{"id":7943,"date":"2024-02-15T23:44:44","date_gmt":"2024-02-15T22:44:44","guid":{"rendered":"https:\/\/genetika-plzen.cz\/?page_id=7943"},"modified":"2026-01-30T09:56:23","modified_gmt":"2026-01-30T08:56:23","slug":"cenik","status":"publish","type":"page","link":"https:\/\/genetika-plzen.nullable.group\/en\/cenik\/","title":{"rendered":"Price list"},"content":{"rendered":"
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The vast majority of all examinations are covered by health insurance. 
<\/b>Below you will find a price list for services, if medical indication is not met<\/b>. <\/p>\n

The above-standard services listed in the price list for self-payers<\/b> are not covered by public insurance. The price is always recalculated with regard to the official current exchange rate. <\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\"\"\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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\n\t\t\t\t\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/i><\/span>\n\t\t\t\t\t\t\t\t<\/i><\/span>\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/span>\n\t\t\t\t\t\t\t\t\t\t\t\tGENETIC TESTING FOR COUPLES<\/a>\n\t\t\t\t\t<\/div>\n\t\t\t\t\t
Carrier test \u2013 NGS Panel, Including Reproductive Disorders (for Insured Persons of Czech Health Insurance)<\/td>3\u00a0500\u00a0K\u010d<\/td><\/tr>
Carrier Test \u2013 Repeated Extended Examination (for Insured Persons of Czech Health Insurance \u2013 previously SMA, CFTR, etc.)<\/td>5\u00a0000\u00a0K\u010d<\/td><\/tr>
Carrier Test \u2013 Self-Payer<\/td>18 500\u00a0K\u010d<\/td><\/tr><\/tbody><\/table><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t
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\n\t\t\t\t\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/i><\/span>\n\t\t\t\t\t\t\t\t<\/i><\/span>\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/span>\n\t\t\t\t\t\t\t\t\t\t\t\tCONSULTATION WITH A CLINICAL GENETICIST<\/a>\n\t\t\t\t\t<\/div>\n\t\t\t\t\t
Targeted Clinical and Genetic Examination Not Yet Concluded (Initial Genetic Consultation)<\/td>1\u00a0500\u00a0K\u010d<\/td><\/tr>
Clinical and genetic screening tests<\/td>300\u00a0K\u010d<\/td><\/tr>
Genetic consultation including sperm analysis<\/td>1 000 K\u010d<\/td><\/tr><\/tbody><\/table><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t
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\n\t\t\t\t\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/i><\/span>\n\t\t\t\t\t\t\t\t<\/i><\/span>\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/span>\n\t\t\t\t\t\t\t\t\t\t\t\tULTRASOUND EXAMINATION<\/a>\n\t\t\t\t\t<\/div>\n\t\t\t\t\t
Superconsultative ultrasound examination \u2013 single pregnancy<\/td>1\u00a0500\u00a0K\u010d<\/td><\/tr>
Superconsultative ultrasound examination \u2013 twins<\/td>2\u00a0500\u00a0K\u010d<\/td><\/tr>
3D\/4D ultrasound (including USB)<\/td>1 500 K\u010d<\/td><\/tr>
Control sonoanatomical examination<\/td>500\u00a0K\u010d<\/td><\/tr>
Ultrasound examination at 30 weeks of pregnancy\u00a0<\/td>1\u00a0000\u00a0K\u010d<\/td><\/tr>
Ultrasound screening for fetal growth restriction in the third trimester of pregnancy\u00a0<\/td>1\u00a0000\u00a0K\u010d<\/td><\/tr>
Fetal reduction<\/td>2 500 K\u010d<\/td><\/tr><\/tbody><\/table>
\u00a0<\/div><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t
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\n\t\t\t\t\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/i><\/span>\n\t\t\t\t\t\t\t\t<\/i><\/span>\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/span>\n\t\t\t\t\t\t\t\t\t\t\t\tINVASIVE PRENATAL DIAGNOSTICS<\/a>\n\t\t\t\t\t<\/div>\n\t\t\t\t\t
examination of the fetus from cells obtained by amniocentesis (AMC) or chorionic villus sampling (CVS)<\/b><\/td><\/tr>
Chromosomal testing of amniotic fluid using the Array CGH method<\/td>10\u00a0000\u00a0K\u010d<\/td><\/tr>
Chromosomal testing of amniotic fluid using Array CGH + QF PCR + consultation<\/td>19\u00a0000\u00a0K\u010d<\/td><\/tr>
Chromosomal testing of chorionic villi + QF PCR + consultation<\/td>19\u00a0000\u00a0K\u010d<\/td><\/tr>
Screening for the most common aneuploidies using QF PCR (AMC or CVS)<\/td>8\u00a0000\u00a0K\u010d<\/td><\/tr><\/tbody><\/table><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t
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\n\t\t\t\t\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/i><\/span>\n\t\t\t\t\t\t\t\t<\/i><\/span>\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/span>\n\t\t\t\t\t\t\t\t\t\t\t\tNON-INVASIVE PRENATAL DIAGNOSTICS<\/a>\n\t\t\t\t\t<\/div>\n\t\t\t\t\t
(fetal examination from the mother's blood)<\/b><\/td><\/tr>
Combined first trimester screening including preeclampsia \u2013 genetic risk assessment \u2013 singleton pregnancy<\/td>2\u00a0000\u00a0K\u010d<\/td><\/tr>
Combined first trimester screening including preeclampsia \u2013 genetic risk assessment \u2013 twins<\/td>3\u00a0000\u00a0K\u010d<\/td><\/tr>
Second Trimester Screening \u2013 Genetic Risk Assessment<\/td>2\u00a0000\u00a0K\u010d<\/td><\/tr>
NIPT (non-invasive testing of fetal DNA from maternal blood)<\/td>12\u00a0500\u00a0K\u010d<\/td><\/tr>
NIPT (non-invasive testing of fetal DNA from maternal blood) + microdeletion<\/td>16 500 K\u010d<\/td><\/tr>
Intramuscular injection<\/td>100\u00a0K\u010d<\/td><\/tr>
Rhesonativ S\/D injection<\/td>1\u00a0100\u00a0K\u010d<\/td><\/tr>
First trimester risk assessment (free \u03b2-hCG, PAPP-A)<\/td>2 000 K\u010d<\/td><\/tr>
Second trimester risk assessment (AFP, hCG)<\/td>1 000 K\u010d<\/td><\/tr><\/tbody><\/table><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t
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\n\t\t\t\t\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/i><\/span>\n\t\t\t\t\t\t\t\t<\/i><\/span>\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/span>\n\t\t\t\t\t\t\t\t\t\t\t\tMOLECULAR GENETIC TESTS<\/a>\n\t\t\t\t\t<\/div>\n\t\t\t\t\t
Examination of thrombophilic status Leiden mutation of the F5 gene<\/td>1\u00a0000\u00a0K\u010d<\/td><\/tr>
Thrombophilic status examination Prothrombin mutations of the F2 gene<\/td>1\u00a0000\u00a0K\u010d<\/td><\/tr>
Examination of Thrombophilic Conditions \u2013 Leiden, Prothrombin<\/td>1\u00a0900\u00a0K\u010d<\/td><\/tr>
Testing for 36 mutations of the CFTR gene (cystic fibrosis)<\/td>9\u00a0000\u00a0K\u010d<\/td><\/tr>
Spinal muscular atrophy testing (MLPA testing of the SMN1 and SMN2 genes)<\/td>3\u00a0000\u00a0K\u010d<\/td><\/tr>
Testing for the most common mutations in the Connexin 26 gene (35delG, W24X)<\/td>3\u00a0000\u00a0K\u010d<\/td><\/tr>
Y chromosome microdeletion testing<\/td>4\u00a0500\u00a0K\u010d<\/td><\/tr>
Examination of the Gilbert syndrome<\/td>3\u00a0500\u00a0K\u010d<\/td><\/tr>
Fragile X Syndrome Testing<\/td>6\u00a0000\u00a0K\u010d<\/td><\/tr>
Hemochromatosis testing<\/td>3\u00a0000\u00a0K\u010d<\/td><\/tr>
Testing for predisposition alleles to celiac disease<\/td>4\u00a0000\u00a0K\u010d<\/td><\/tr>
Examination of Nijmegen breakage syndrome<\/td>2\u00a0500\u00a0K\u010d<\/td><\/tr>
Lactose intolerance test<\/td>4\u00a0000\u00a0K\u010d<\/td><\/tr>
DNA isolation<\/td>1\u00a0000\u00a0K\u010d<\/td><\/tr>
Isolation and preservation of DNA for 5 years<\/td>3\u00a0500\u00a0K\u010d<\/td><\/tr>
Serological Examination from Amniotic Fluid \u2013 Toxoplasmosis<\/td>2 000 K\u010d<\/td><\/tr>
HLA B27 Examination \u2013 Ankylosing Spondylitis<\/td>1 800 K\u010d<\/td><\/tr>
Smith-Lemli-Opitz syndrome (SLO syndrome) screening (3 mutations)<\/td>2 500 K\u010d<\/td><\/tr><\/tbody><\/table>
\u00a0<\/div><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t
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\n\t\t\t\t\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/i><\/span>\n\t\t\t\t\t\t\t\t<\/i><\/span>\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/span>\n\t\t\t\t\t\t\t\t\t\t\t\tCYTOGENETIC EXAMINATION<\/a>\n\t\t\t\t\t<\/div>\n\t\t\t\t\t
Peripheral blood karyotype examination<\/td>5\u00a0000\u00a0K\u010d<\/td><\/tr>
Examination of acquired chromosomal aberrations<\/td>5\u00a0000\u00a0K\u010d<\/td><\/tr>
Molecular cytogenetic testing using the a-CGH method<\/td>10\u00a0000\u00a0K\u010d<\/td><\/tr>
FISH testing depending on the number of probes<\/td>od 9\u00a0500\u00a0K\u010d<\/td><\/tr><\/tbody><\/table>
\u00a0<\/div><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t
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\n\t\t\t\t\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/i><\/span>\n\t\t\t\t\t\t\t\t<\/i><\/span>\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/span>\n\t\t\t\t\t\t\t\t\t\t\t\tREPRODUCTIVE GENETICS TESTING<\/a>\n\t\t\t\t\t<\/div>\n\t\t\t\t\t
PGT-A of 24 chromosomes using NGS (price per embryo)<\/td>5 600 K\u010d<\/td><\/tr>
Verification of the presence of a familial mutation<\/td>12 500 K\u010d<\/td><\/tr>
KIR + HLA-C analysis (pair)<\/td>8 000 K\u010d<\/td><\/tr>
PGT-M preparation set-up before PGT-M<\/td>5 000 K\u010d<\/td><\/tr>
PGT-M using the Karyomapping method + basic PGT-A of 24 chromosomes (up to 2 embryos)<\/td>71 500 K\u010d<\/td><\/tr>
PGT-M using the Karyomapping method + basic PGT-A of 24 chromosomes (up to 5 embryos)<\/td>96 000 K\u010d<\/td><\/tr>
PGT-M using the Karyomapping method + basic PGT-A of 24 chromosomes (for each additional embryo starting from the 6th)<\/td>12 500 K\u010d<\/td><\/tr>
PGT-M Direct diagnosis (special case)<\/td>15 600 K\u010d<\/td><\/tr>
PGT-SR and PGT-A of 24 chromosomes using NGS (price per embryo)<\/td>6 400 K\u010d<\/td><\/tr><\/tbody><\/table>
\u00a0<\/div><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t
\n\t\t\t\t\t
\n\t\t\t\t\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/i><\/span>\n\t\t\t\t\t\t\t\t<\/i><\/span>\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/span>\n\t\t\t\t\t\t\t\t\t\t\t\tONCOGENETIC EXAMINATIONS<\/a>\n\t\t\t\t\t<\/div>\n\t\t\t\t\t
Oncopanel<\/td>26\u00a0000\u00a0K\u010d<\/td><\/tr>
(ATM,APC,BARD1, BRCA1, BRCA2, BRIP1, CDH1, CHEK2, EPCAM,MLH1, MSH2, MSH6, MUTYH,NBN,PALB2, PMS2, PTEN,RAD50,RAD51C, RAD51D,STK11,TP53)<\/td><\/tr>
Detection of a known mutation of a gene from the oncology panel<\/td>3\u00a0500\u00a0K\u010d<\/td><\/tr><\/tbody><\/table>
\u00a0<\/div><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t
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\n\t\t\t\t\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/i><\/span>\n\t\t\t\t\t\t\t\t<\/i><\/span>\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/span>\n\t\t\t\t\t\t\t\t\t\t\t\tPATERNITY TESTS<\/a>\n\t\t\t\t\t<\/div>\n\t\t\t\t\t
Paternity Test without Expert Opinion \u2013 Father + Child<\/td>5\u00a0900\u00a0K\u010d<\/td><\/tr>
Paternity Test without Expert Opinion \u2013 Father + Child + Mother<\/td>6\u00a0900\u00a0K\u010d<\/td><\/tr>
Paternity Test without Expert Opinion \u2013 3 Persons<\/td>7\u00a0900\u00a0K\u010d<\/td><\/tr>
combination: 2x father + 1x child \/ 1x father + 2x child<\/td><\/tr>
Testing another person in addition to the test already performed (another father, another child)<\/td>2 900 K\u010d<\/td><\/tr>
Paternity Test including Expert Opinion \u2013 Father + Child<\/td>12\u00a0000\u00a0K\u010d<\/td><\/tr>
Paternity Test including Expert Opinion \u2013 Father + Child + Mother<\/td>13\u00a0000\u00a0K\u010d<\/td><\/tr><\/tbody><\/table>
\u00a0<\/div><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t
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\n\t\t\t\t\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/i><\/span>\n\t\t\t\t\t\t\t\t<\/i><\/span>\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/span>\n\t\t\t\t\t\t\t\t\t\t\t\tADMINISTRATIVE TASKS<\/a>\n\t\t\t\t\t<\/div>\n\t\t\t\t\t
Photos on request (2 images)<\/td>150\u00a0K\u010d<\/td><\/tr>
Obtaining copies and extracts of documentation<\/td>150\u00a0K\u010d<\/td><\/tr>
USG photography<\/td>150\u00a0K\u010d<\/td><\/tr>
3D \u2013 USG fotografie<\/td>550\u00a0K\u010d<\/td><\/tr>
Color Photo \u2013 A5 (price per piece)<\/td>100 K\u010d<\/td><\/tr><\/tbody><\/table>
\u00a0<\/div><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t
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\n\t\t\t\t\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/i><\/span>\n\t\t\t\t\t\t\t\t<\/i><\/span>\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/span>\n\t\t\t\t\t\t\t\t\t\t\t\tIMMUNOLOGY CLINIC<\/a>\n\t\t\t\t\t<\/div>\n\t\t\t\t\t
IMMUNOLOGICAL EXAMINATION OF WOMEN<\/b><\/td>price<\/b><\/td><\/tr>
Consultation and report for the entire couple in the field of reproductive immunology<\/td>4\u00a0000\u00a0K\u010d<\/td><\/tr>
Blood sampling<\/td>200\u00a0K\u010d<\/td><\/tr>
Examinations<\/td>300\u00a0K\u010d<\/td><\/tr>
Colposcopy + ovulation mucus sampling<\/td>300\u00a0K\u010d<\/td><\/tr>
Antibodies against sperm in blood serum<\/td>300\u00a0K\u010d<\/td><\/tr>
Antibodies against sperm in blood serum \u2013 iMAR test<\/td>1 500 K\u010d<\/td><\/tr>
Antizonal antibodies in blood serum<\/td>300\u00a0K\u010d<\/td><\/tr>
Antiphospholipid antibodies \u2013 profile in blood serum\u00a0<\/td>12\u00a0000\u00a0K\u010d<\/td><\/tr>
anti-cardiolipin IgG, IgM<\/td><\/tr>
Beta2-glycoprotein IgG, IgA<\/td><\/tr>
Annexin V, IgG, IgM<\/td><\/tr>
Phosphatidyl serine IgG, IgM<\/td><\/tr>
Phosphatidylinositol IgG, IgM<\/td><\/tr>
Phosphatidic acid IgG, IgM<\/td><\/tr>
Phosphatidylethanolamine IgG, IgM<\/td><\/tr>
Antibodies against sperm in ovulatory secretions \u2013 iMAR test<\/td>1\u00a0500\u00a0K\u010d<\/td><\/tr>
Antibodies against sperm in ovulatory secretions \u2013 Kremer test<\/td>200\u00a0K\u010d<\/td><\/tr>
Total<\/b><\/td>20\u00a0600\u00a0K\u010d<\/b><\/td><\/tr>
\u00a0<\/b><\/td>\u00a0<\/td><\/tr>
IMMUNOLOGICAL EXAMINATION OF MEN<\/b><\/td>price<\/b><\/td><\/tr>
Blood sampling<\/td>200\u00a0K\u010d<\/td><\/tr>
Antibodies against sperm in blood serum<\/td>300\u00a0K\u010d<\/td><\/tr>
Antibodies against sperm in blood serum \u2013 iMAR test<\/td>1 500 K\u010d<\/td><\/tr>
Sperm analysis (ejaculate)<\/td>1\u00a0000\u00a0K\u010d<\/td><\/tr>
MAR test (ejaculate)<\/td>1\u00a0500\u00a0K\u010d<\/td><\/tr>
Intrachromosomal enzymes Hs8, Hs14<\/td>2\u00a0000\u00a0K\u010d<\/td><\/tr>
Measurement of Sperm Oxidative Stress<\/td>2\u00a0500\u00a0K\u010d<\/td><\/tr>
Total<\/b><\/td>9 000 K\u010d<\/b><\/td><\/tr><\/tbody><\/table><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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<\/div>\n\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>","protected":false},"excerpt":{"rendered":"

Naprost\u00e1 v\u011bt\u0161ina v\u0161ech vy\u0161et\u0159en\u00ed je hrazena ze zdravotn\u00edho poji\u0161t\u011bn\u00ed. N\u00ed\u017ee naleznete cen\u00edk slu\u017eeb, pokud k nim nen\u00ed spln\u011bna medic\u00ednsk\u00e1 indikace.  Nadstandardn\u00ed slu\u017eby uveden\u00e9 v cen\u00edku pro samopl\u00e1tce (n\u00ed\u017ee) nejsou hrazeny ze zdravotn\u00edho poji\u0161t\u011bn\u00ed.  GENETICK\u00c9 TESTOV\u00c1N\u00cd PRO P\u00c1RY Carrier test \u2013 NGS\u00a0panel, v\u010detn\u011b Poruch Reprodukce (pro poji\u0161t\u011bnce ZP \u010cR) 3\u00a0500\u00a0K\u010d Carrier test \u2013 opakovan\u00e9 roz\u0161\u00ed\u0159en\u00e9 vy\u0161et\u0159en\u00ed (pro […]<\/p>","protected":false},"author":9,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"service-area":[38],"class_list":["post-7943","page","type-page","status-publish","hentry","service-area-cenik"],"yoast_head":"\nCen\u00edk | Genetika 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\u010cR) 3\u00a0500\u00a0K\u010d Carrier test \u2013 opakovan\u00e9 roz\u0161\u00ed\u0159en\u00e9 vy\u0161et\u0159en\u00ed (pro […]\" \/>\n<meta property=\"og:url\" content=\"https:\/\/genetika-plzen.nullable.group\/en\/cenik\/\" \/>\n<meta property=\"og:site_name\" content=\"Genetika Plze\u0148\" \/>\n<meta property=\"article:modified_time\" content=\"2026-01-30T08:56:23+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/www.genetika-plzen.cz\/wp-content\/uploads\/2024\/02\/thumb_3000x3000_cenikec92-1024x683.jpg\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Estimated reading time\" \/>\n\t<meta name=\"twitter:data1\" content=\"5 minutes\" \/>\n<script type=\"application\/ld+json\" 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