NIPT Amity
Ensure your baby’s health with non-invasive, accurate prenatal screening
NIPT provides accurate detection of genetic conditions with a simple blood test. Gain insights into your baby's health
Explore Your Baby’s Health with Precision Using Our Advanced NIPT, Offering Early Detection of Genetic Conditions
Test Advantages
Early detection of genetic conditions
Insight into baby's health
Accurate and reliable results
Simple blood test
NIPT Amity
The NIPT at Genome X is a state-of-the-art, non-invasive test designed to screen for genetic conditions in your baby with exceptional accuracy. By analyzing a simple maternal blood sample, this test provides comprehensive insights into your baby’s health, helping you understand potential genetic risks early on. With reliable and detailed results, this test ensures that you can make informed decisions with confidence and peace of mind about your pregnancy and your baby’s well-being.
Experience the Future of Genetic Testing with Our State-of-the-Art Solutions, Delivering Accurate Results and Comprehensive Support
NIPT Amity Lite offers a non-invasive prenatal test to screen for key genetic conditions through a simple blood sample. This test evaluates:
Trisomy 13 (Patau Syndrome)
Trisomy 18 (Edwards Syndrome)
Trisomy 21 (Down Syndrome)
Sex Chromosome Abnormalities
Optional Microdeletions (8 or 116)
Gain early insights into your baby's genetic health with NIPT Amity Lite, providing essential information for informed pregnancy decisions.
NIPT Amity Basic offers a non-invasive prenatal test that screens for:
Trisomy 13 (Patau Syndrome)
Trisomy 9
Trisomy 16
Trisomy 21 (Down Syndrome)
Trisomy 22
Sex Chromosome Abnormalities
Optional Microdeletions (8 or 116)
This test provides essential insights into your baby's genetic health through a simple blood sample, helping you make informed decisions about your pregnancy.
NIPT Amity Premium offers a comprehensive non-invasive prenatal test that screens for:
All Chromosomes
Optional Microdeletions (8 or 116)
This advanced test provides detailed insights into your baby's genetic health, including an extensive analysis of all chromosomes and specific microdeletions, using just a simple blood sample. It's designed to give you the most thorough understanding of your baby's genetic profile for informed decision-making.
Test Procedure
Genome X Test Procedure
A simple blood or saliva sample is collected from both partners.
Our lab uses advanced genetic sequencing technologies.
The samples are securely shipped to our laboratory.
Comprehensive genetic tests are conducted.
You receive a detailed report explaining the findings.
Key Features
Genome X Test Features
Swift Results
Test results delivered within 5 to 7 working days, ensuring top-notch service and accuracy.
Affordance
High-quality genetic testing made affordable, offering transparent pricing and exceptional value.
Reliable Results
High quality testing achieved through international collaborations to ensure precision and global expertise.
Confidential
Testimonials
Our Patients Reviews
"The genetic testing was accurate and fast—really impressed with the level of detail provided. Excellent service!"
