Getchecked NIPT® – Non-Invasive Prenatal Testing at Getchecked

Get your results within 5 business days. Getchecked NIPT offers genetic, non-invasive prenatal testing (NIPT) to screen for the most common fetal chromosomal abnormalities. Our test combines the latest next generation sequencing technology with expert medical reporting.

With Getchecked NIPT Now Offers Non-Invasive Prenatal Testing That Provides a Fast and Accurate Screen for the Most Common Prenatal Chromosomal Abnormalities.*

Getchecked NIPT is performed on a single maternal blood sample and combines the latest next generation sequencing technology with the highest quality medical reporting. It provides unparalleled accuracy and detection compared to other non-invasive testing methods – ultrasonography or nuchal translucency testing.

Our medical expertise is ideally suited to provide you and your patients with reliable, well supported result interpretation.

Why Choose GetcheckedNIPT?

100% SAFE

Only 9ml of maternal blood required


Test performed from the 10th gestational week


Highly accurate results available within 5 business days


Getchecked NIPT kit free of charge. Return shipment via phone call

Expertise You Can Trust

Conventional prenatal testing for fetal chromosomal abnormality involves either chorionic villus sampling or amniocentesis. These procedures are highly invasive and carry an elevated risk of miscarriage, but despite this have become standard practice worldwide due to their high levels of accuracy and the range of abnormalities they can detect.

Approximately 1% of All Babies Will Be Born With a Chromosomal Abnormality





Trisomy 21 (Down syndrome
Trisomy 18 (Edwards syndrome)
Trisomy 13 (Patau syndrome)

Sex Chromosome Aneuploidies & Fetal Gender

Sex Chromosome Aneuploidies

Concordance with cytogenetic results

100.0 %
100.0 %
X0 (Turner syndrome
90.5 %
XXX (Triple X syndrome)
100.0 %
XXY (Klinefelter syndrome)
100.0 %
XYY (Jacobs syndrome)
91.7 %

GetcheckedNIPT Reporting Information

Getcheked NIPT is only designed to analyze chromosome aneuploidies of the fetus after 10 weeks of gestation. Reported are overrepresentations of chromosomes 21, 18 and 13, as well as the sex chromosome aneuploidies XO, XXX, XXY and XYY. This screening test does not test for aneuploidies in other chromosomes not mentioned above and can therefore not exclude abnormalities in these.

Chromosome aneuploidies for a twin gestation can in general be detected by this test. However, the test cannot be attributed to individual twin fetuses because in twin gestations sensitivity and specificity for detection of aneuploidies are limited. In case of twin pregnancy and detection of only one Y chromosome by the test, the fetal gender of each individual twin cannot be determined by the test.

Getchecked Reports NIPT Results As Follows:

Positive result – if Getchecked NIPT identifies an aneuploidy (chromosome 21, 18, 13 or gonosomal chromosomes), Getchecked NIPT reports presence of aneuploidy and provides data on fetal DNA fraction in the sample of mother´s peripheral blood (in percentages) and the data on fetal gender if requested. We urgently recommend to the referring physician or the genetic counselor to determine and decide if further invasive testing and subsequent analysis is needed.

Negative result – if NIPT did not indicate a trisomy of chromosome 13, 18, or 21 or gonosomal abnormalities, Getchecked Clinic reports a negative result together with the data on fetal DNA fraction and the data on fetal gender if requested. A negative result cannot entirely exclude the possibility of fetoplacental mosaicism. Thus, Getchecked Clinic is giving negative results of NIPT together with the suggestion: if the fetus shows abnormalities on ultrasound investigation, or if a family history of fetal abnormalities or other genetic disorders exists, we urgently recommend to the referring physician or the genetic counselor to determine and decide if further invasive testing and subsequent analysis is needed.

In the very unlikely case of inconclusive results of the non-invasive prenatal testing due to the limitation of the system, we recommend further follow-up of the fetal growth using ultrasound as well as 2nd trimester screens. In case of any abnormalities observed on the ultrasound examination or if there is a positive family history of fetal abnormalities or other genetic disorders, we highly suggest invasive testing and subsequent analysis.


Sample Preparation and analysis software are CE-IVD marked

Noninvasive prenatal testing (NIPT) based on cell-free DNA analysis from maternal blood is a screening test; it is not diagnostic. Test results must not be used as the sole basis for diagnosis. Further confirmatory testing is necessary prior to making any irreversible pregnancy decision.

Getchecked Clinic's NIPT Is the Earliest and Most Accurate Way To Detect Trisomy 21

Conventional Prenatal Screening Methods vs. GetcheckedNIPT

how it works

Book in Clinic or Home

Visit or We’ll Visit You: Start your journey either by visiting our clinic or opting for our convenient home collection service.

FDA Approved Laboratory

Global Laboratory Analysis: Your sample is sent to one of the world’s leading laboratories, ensuring top-notch accuracy and reliability.

Personalized Health Plan

Comprehensive Insights: Within 10 days, receive your detailed genetic report and Free Consultation. Your path to personalized health insights begins here.


If you have a query, no matter how small or significant we’ll do our best to assist you. You can call us using the number provided or open a Live Chat with one of our agents.
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