For self-payers, examinations are not paid from health insurance, and the examination does not satisfy a medical indication
| Genetic consultation with medical doctor/geneticist | |
| Targeted clinical – genetic examination, not yet closed | 1 500 CZK |
| Clinical – genetic control/final consultation | 300 CZK |
| Spermiogram examination, including consultation | 800 CZK |
| Ultrasound examination | |
| 1st trimester ultrasound examination including certified NT measurement (Nuchal translucency) | 1 600 CZK |
| 2nd trimester detailed ultrasound examination including fetal heart and morphology examination | 1 600 CZK |
| 3rd trimester ultrasound screening examination of fetal morphology | 1 600 CZK |
| 3D / 4D ultrasound (including DVD) – non-medical performance | 1 600 CZK |
| Screening prenatal examination | |
| Assessment of genetic risk in the 1st + 2nd trimester (integrated test) | 600 CZK |
| Non-invasive prenatal examination | |
| Non-invasive prenatal testing | 12 500 CZK |
| Invasive prenatal examination | |
| Chromosomal examination of amniotic fluid | 5 000 CZK |
| Examination of the most common aneuploidies by QF PCR | 7 000 CZK |
| Chromosomal examination of amniotic fluid + QF PCR | 10 000 CZK |
| Chromosomal examination of chorionic villus + QF PCR | 12 000 CZK |
| Amniotic fluid examination by QF PCR + Array CGH | 20 000 CZK |
| Chorionic villus examination by QF PCR + Array CGH | 20 000 CZK |
| Cytogenetic and molecular cytogenetic examinations | |
| Examination of karyotype | 4 000 CZK |
| Chromosomal breakage analysis | 2 000 CZK |
| FISH method (price depends on the number of examined probes) | from 9 500 CZK |
| Array CGH examination | 10 000 CZK |
| Molecular genetic examinations | |
| DNA banking – DNA isolation and storage | 1 000 CZK |
| Thrombophilic mutations – Leiden, Protrombin | 2 000 CZK |
| Microdeletions of Y chromosome | 4 500 CZK |
| Cystic fibrosis (34 mutations of CFTR gene) | 9 000 CZK |
| Fragile X syndrome | 6 000 CZK |
| Spinal muscular atrophy (SMA) | 4 500 CZK |
| Predisposition to gluten intolerance (celiac disease) | 4 000 CZK |
| Predisposition to hereditary oncological diseases (NGS panel sequencing) | 23 000 CZK |
| Detection of known familial gene mutation (Sanger sequencing/MLPA) | 4 000 CZK |