This advanced test screens for microdeletions that can affect learning, growth, and organ function. Panorama Microdeletion NIPT helps you uncover serious risks that standard tests may miss.
Fast lab processing means most parents receive their results within a few working days.
Panorama Microdeletions NIPT includes the test, secure sample collection, analysis, and a consultation with a Jeen genetic counsellor.
Conditions like Trisomy 21, 18, and 13 can occur even without family history. Screening helps identify risk early in pregnancy.
*This number is based on UK prevalence data for conditions screened by Natera's Panorama Microdeletions panel.
Disclaimer! The information provided in this article is for educational purposes only and is based on NHS recommendations. It is not a substitute for professional medical advice. Always consult your doctor or a qualified healthcare provider for advice on medical conditions or treatments.
Panorama screens for a select group of well-characterised microdeletion syndromes, including:
Microdeletions are small missing segments of DNA on specific chromosomes. These missing pieces can affect several genes, often leading to developmental delays, learning disabilities, physical differences, or medical conditions. Unlike more common conditions like Down’s syndrome, microdeletions may not be picked up in standard screening, making early detection with Panorama especially valuable.
From just a single maternal blood draw at 9 weeks, Panorama Microdeletions can assess your baby’s risk for a range of rare genetic conditions. The sample is processed in a state-of-the-art US laboratory, where specialised genomic analysis and AI-driven technology are used to identify tiny missing segments of DNA. You’ll typically receive your results within 7 to 10 working days, giving you early insight with no risk to your pregnancy.
Panorama Microdeletion screening is not available for:
This screening also has these limitations:
Panorama Microdeletions is an ideal option for parents who want to screen for rare but serious genetic conditions that may not be covered by standard NIPT. It may be especially suitable if:
Please note: Panorama Microdeletions screening is only available for singleton pregnancies and is not recommended for twin pregnancies, egg donation, or vanishing twin cases.
Basic and advanced PrenatalSafe options compared to help you choose the right test for your pregnancy.
Basic NIPT screens for the three most common chromosomal conditions: Down’s syndrome (Trisomy 21), Edwards’ syndrome (Trisomy 18), and Patau’s syndrome (Trisomy 13). Advanced NIPT includes everything in the basic test, but can also check for sex chromosome conditions, some rare genetic deletions (called microdeletions), and can tell you the biological sex of the baby if you choose to know. At Jeen, our genetic counsellors will help you decide which version is right for you during your consultation.
We ask you to send us your scan so our medical team can confirm that you’re at least 10 weeks pregnant and that the pregnancy appears to be developing normally. This helps us ensure the test is appropriate and that the results will be accurate. It’s also important to understand that NIPT only screens for specific genetic conditions. It does not detect structural anomalies, such as heart defects or issues with organ development, which are physical rather than genetic. These types of conditions are usually picked up later in pregnancy through detailed ultrasound scans. Sending your early scan allows our doctors to check for any concerns before moving forward with the NIPT.
No - genetic testing shows your risk, not a guarantee. Some people with a genetic variant never develop the condition, while others without a variant might still be affected due to lifestyle or environmental factors.
Yes, NIPT can usually identify the baby’s biological sex with high accuracy, but this is completely optional. If you’d like to know, just let your genetic counsellor know during your consultation — and if you’d rather not find out, we’ll make sure it’s not included in your report.
At the moment, NIPT is only offered through the NHS in certain cases — for example, if you’ve had a high-risk result from a standard screening test. At Jeen, we offer private NIPT testing with flexible options, fast results, and full clinical support, including at-home appointments and expert guidance.
Your results will usually be ready within 2–10 working days from the time your sample arrives at our partner lab. The exact turnaround time depends on which NIPT you’ve chosen and the location of the laboratory. We’ll keep you informed throughout the process and arrange a follow-up consultation to talk you through your results as soon as they’re ready.
Please note that delays can occur during public holidays in both the UK and the US. If your results indicate that follow-up testing is needed for your partner, we’ll act quickly to keep everything moving smoothly. Our priority is to get you the answers you need without unnecessary delays — so you can make confident, informed decisions for your pregnancy.
You can take the NIPT from 10 weeks into your pregnancy. Before booking your test with Jeen, we ask you to send us a recent pregnancy scan, such as a dating or viability scan, so our team of specialists can confirm you’re eligible to proceed.
Yes, NIPT is completely safe for both you and your baby. It’s a non-invasive blood test that only requires a small sample from your arm, and there is no physical contact with the baby. This means there is no risk of miscarriage or harm to the pregnancy, unlike some invasive procedures.
NIPT is over 99% accurate at detecting Down’s syndrome and also highly reliable for Edwards’ and Patau’s syndromes. It is more accurate than standard NHS screening and produces fewer false positive results, which means fewer people are sent for unnecessary follow-up testing.
Yes, at Jeen we believe it’s important that everyone taking NIPT has a chance to speak to a qualified genetic counsellor first. This session helps you understand what the test covers, what it doesn’t, and what the results might mean for you and your baby. It’s a space to ask any questions and make confident, informed choices.
If your result shows a high risk for a condition, we’ll arrange a follow-up session with one of our genetic counsellors to explain exactly what it means. You’ll be given the option to have a diagnostic test, such as amniocentesis or CVS, which can confirm the result. We’ll support you at every step, with clear information and no pressure.
No, NIPT screens for a specific set of genetic conditions, mostly involving extra or missing chromosomes. It won’t detect all birth defects or structural anomalies, such as heart defects or limb differences. That’s why it’s important to still attend all your routine scans and check-ups during pregnancy.
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