Why choose KNOVA Full Panel NIPT?
KNOVA is ideal for parents who want the most detailed and comprehensive prenatal screening available.
- Cutting-edge technology: Built by Fulgent Genetics, KNOVA uses next-generation sequencing to offer highly accurate results with a wide detection range.
- Ideal for high-risk pregnancies: If your baby has a raised nuchal translucency (NT) or ultrasound concern, KNOVA provides detailed information that may help avoid invasive testing.
- All-in-one test: There’s no “basic” version of KNOVA. Every test includes its full, extended panel so you never miss a key result.
- Unmatched screening power: KNOVA screens for more conditions than any other NIPT.
- Optional Gender Reveal: Find out your baby’s sex with over 99% accuracy, if you wish.
What conditions does KNOVA screen for?
KNOVA offers the broadest panel of any NIPT, detecting both chromosomal and monogenic conditions. It’s built with Fulgent’s industry-leading sequencing platform, capable of analysing over 18,000 human genes.
- All major trisomies: Down’s (21), Edwards’ (18), Patau (13), plus rare trisomies (15, 16, 22)
- Sex chromosome conditions: Turner and Klinefelter syndromes, and more
- 56 single-gene (monogenic) disorders: Like Noonan syndrome, CHARGE, Cornelia de Lange, tuberous sclerosis, skeletal dysplasias.
- 12 microdeletion syndromes: Including DiGeorge syndrome (22q11.2).
What are the limitations of KNOVA?
While KNOVA is the most complete prenatal screening available, it isn’t suitable for every pregnancy. KNOVA cannot be used in the following situations:
- Twin or triplet pregnancies
- Pregnancies with egg donation
- Cases of vanishing twin syndrome
- Mothers with a history of bone marrow or organ transplant
- Parental mosaicism or chromosomal abnormalities
KNOVA is also a screening test, not a diagnostic one. If any result shows a high risk, you may still need further testing (like CVS or amniocentesis) to confirm the result.
Who Should Consider KNOVA NIPT?
KNOVA is recommended for parents who:
- Want the most advanced and thorough genetic screening available.
- Have seen a raised NT or abnormal findings on early ultrasound.
- Prefer to avoid amniocentesis or CVS unless absolutely necessary
- Want reassurance about rare genetic syndromes and single-gene conditions.
- Have a family history of complex or unexplained conditions.
KNOVA is one of the most advanced NIPT in the UK, available through Jeen. Book your appointment today and take the next step in understanding your baby’s genetic health.
What Are My Blood Draw Options for KNOVA NIPT?
In line with our flexible, prevention-first approach, Jeen Health offers multiple convenient options for how you provide your DNA sample for KNOVA NIPT:
- Self-Arranged Blood Draw (Free): We'll send your KNOVA NIPT kit and you can then arrange your own blood draw with a local nurse, midwife, phlebotomy service, or clinic. Many patients ask their private GP, or maternity care provider to assistPlease ensure your provider is comfortable drawing into the NIPT-specific tubes supplied in your kit. If needed, we can share instructions.
- Best if you already have a provider you trust
- No added charge from Jeen, but you may need to pay your chosen provider directly
- Nationwide availability across the UK and some EU region
- Jeen Clinic Network (+£40): Prefer a clinic-based option? Book a blood draw appointment at one of our 40+ trusted partner locations across the UK.
- Home Visit (+£65): Need maximum convenience? We’ll send a qualified nurse to your home to take your blood sample.
- Ideal for patients with mobility, time or privacy needs
- Available across most of the UK and appointments coordinated by our team
These sample collection options ensure NIPT is accessible on your terms.































