We assess the risk of Down syndrome and other chromosomal conditions in your baby
Book the test
Geneticist's consultation included
Results from 4 days
NGS technology
An internationally trained teamWhat is NIPT
From week 10 of pregnancy, NIPT assesses these risks from an ordinary blood test of the mother. Based on the results, a geneticist chooses a personal plan for the pregnancy.
Who is NIPT for?
Prices
Screening for 3 chromosomal conditions
3 500 000 UZS
+400 000 UZS for express results in 4 days
Down syndrome (trisomy 21)Edwards syndrome (trisomy 18)Patau syndrome (trisomy 13)The baby's sexSuitable for twinsFree geneticist's consultationResults in 12 working days
Extended screening for 86 chromosomal conditions
3 900 000 UZS
+400 000 UZS for express results in 4 days
Everything in BasicSex chromosome conditions19 rare trisomies60 microdeletion syndromes
Not suitable for twinsFree geneticist's consultationResults in 12 working days
Leave your number and we will call you to arrange a time.
A nurse takes a small sample of blood from a vein.
In 8–12 working days, or in 4 days with express testing.
The doctor explains the results and tells you whether any other tests are needed.
Why GeneHUB
In prenatal diagnostics, this means every mother-to-be can get reliable information about her baby's health early in pregnancy.
How do we do it?
We run next-generation sequencing in our own local laboratory: no international shipping risks and less time from the blood draw to the decoded data.
Every step, from the blood draw to bioinformatic analysis and validation of results, follows strict international protocols that keep the data reproducible and confidential.
Our advantages
A validated technology: 100% sensitivity and 99.95% specificity in studies.
A geneticist explains the results and gives personal advice on what to do next.
GeneHUB specialists trained at the universities of Pavia, Seoul, Athens and Saint Petersburg.
The test is done entirely in the GeneHUB laboratory. Genetic data never leave the country.
Medical activity under licence No. 2384 of 14.02.2024.
One blood test and a geneticist's consultation give you important answers
Doctors
Geneticist, over 9 years of experience
Graduated from the Tashkent State Medical University and trained in Moscow (Russia). Specialises in molecular genetic diagnostics, PCR and NGS, and finding mutations and hereditary conditions.
Head of the GeneHUB laboratory, over 4 years of experience
Graduated from the Tashkent Medical Academy in medical biology. Experienced in laboratory diagnostics and molecular genetics, trained in Almaty and Moscow.
Molecular geneticist and bioinformatician, over 4 years of experience
Studied and did research at the universities of Pavia (Italy) and Athens (Greece). Specialises in NGS sequencing and bioinformatics, and researched cancer on 3D cell models.
Geneticist, over 7 years of experience
Graduated from the Tashkent State Medical University and did research at UNIST (South Korea). Specialises in hereditary conditions and reproductive and prenatal genetics, and studied stem cells.
Reading the results
Trisomy 21 (Down syndrome)
Trisomy 18 (Edwards syndrome)
Trisomy 13 (Patau syndrome)
Fetal fraction3 — 6.8%
Enough for a reliable result (at least 3.5%)
The baby's sex — Female
Determined from the mother's blood (on request)
Questions
In studies the test has 100% sensitivity and 99.95% specificity. It is one of the most accurate non-invasive methods.
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