NIPT Pro
Deeper insight, trusted by most expectant parents.
NIPT Pro is a non-invasive prenatal test that detects Down syndrome, DiGeorge syndrome, and more than 100 other conditions from as early as week 10 of pregnancy. Unlike NIPT Basic, Standard and Plus tests, NIPT Pro looks deeper and further, detecting even smaller changes that matter for your baby’s future health.

Trusted by more than 4,000 doctors worldwide
NIPT Pro is our best-selling prenatal test
It tests for the widest panel of genetic conditions, using whole genome sequencing across all 46 chromosomes. Whole genome sequencing enables detection of all major trisomies, sex chromosome aneuploidies, and 92 deletion/duplication syndromes. With the deepest sequencing depth (averaging 30 million reads) and highest resolution on the market (up to 3 Mbp), NIPT Pro delivers very reliable results, while detecting small genetic changes that can seriously affect child’s health.
It screens for
Down (trisomy 21), Edwards (trisomy 18), and Patau (trisomy 13) syndrome
Sex chromosome aneuploidies (e.g. Turner and Klinefelter syndrome)
94 deletion/duplication syndromes, incl. DiGeorge 1 syndrome
Trisomies 9, 16, 24
All other trisomies, monosomies and deletions/duplications bigger than 5 Mbp if you select incidental findings
Optional: Gender information
Have one worry less with NIPT by GenePlanet
Fast results in 6-10 days
Requires only a small sample of blood – completely safe for the baby
More than 99% reliable results for most common trisomies
Analysed in state-of-the-art NGS EU-based lab



More reliable thanks to superior technology
Would you trust a blurry photo to make a life decision?
NIPT Pro delivers crystal-clear genetic insights thanks to:
Highest sequencing depth
Highest sequencing depth for more reliable results: an average of 30 million reads is far more than many other tests that use around 10-25 million reads. Each DNA fragment is checked multiple times, so we don’t miss anything important.
Highest resolution
Highest resolution for detecting small DNA changes with serious outcome. It can detect genetic changes as small as 3 million base pairs – that’s over 2x more detailed than many other tests, which often detect only changes larger than 7 million base pairs.
Because your baby deserves the sharpest picture of health.
All NIPT by GenePlanet packages give you reliable answers.
But with NIPT Pro, you benefit from upgraded technology that looks even closer at your baby’s DNA.
NIPT Plus — The essentials
Sequencing depth: up to 25 million reads
Detects 60 larger deletions and duplications (over5 Mbp)
Perfect if you want to check the most common genetic conditions and larger structural DNA changes.
NIPT Pro — See more, know more
Ultra-deep sequencing: an average of 30 million reads
Detects 92 smaller deletions and duplications (from 3 Mbp), many different from Plus – including DiGeorge syndrome
Ideal if you want broader insight and want to minimize the risk of missing even smaller DNA changes with serious impact on your baby’s health.
How do I do the test?
Choose your gynaecologist
Give a small blood sample from the arm
Get results in just 6–10 days

Expand NIPT Pro with additional analyses

CF & SMA Carrier
Screen if you carry a gene variant for cystic fibrosis and spinal muscular atrophy
Learn more