All test packages

27 specialized panels — pick what fits your needs.

Prenatal Care

17 packages

Geno NIPT 3

1 tests · Turnaround 2–4 days

Screens for three common chromosomal conditions: Down syndrome (T21), Edwards syndrome (T18) and Patau syndrome (T13).

Geno NIPT 4

1 tests · Turnaround 2–4 days

Screens for Down, Edwards and Patau syndromes, combined with assessment of sex chromosome (X, Y) number abnormalities.

Geno NIPT 4 Thalass

1 tests · Turnaround 2–4 days

Screens for three common syndromes and sex chromosome abnormalities, with assessment of the risk of carrying a Thalassemia gene.

Geno NIPT 7

1 tests · Turnaround 2–4 days

Screens for three common syndromes and four sex chromosome conditions: Turner, Klinefelter, Triple X and Jacobs.

Geno NIPT 7 Plus

1 tests · Turnaround 2–4 days

Includes the full Geno NIPT 7 panel plus screening for maternal carrier risk of selected recessive conditions such as Thalassemia, SMA and G6PD deficiency.

Geno NIPT 23

1 tests · Turnaround 2–4 days

Screens chromosome number abnormalities across all 23 fetal chromosome pairs: 22 autosomal pairs and one sex chromosome pair.

Geno NIPT 23 Plus

1 tests · Turnaround 2–4 days

Screens all 23 fetal chromosome pairs and 21 common maternal recessive genetic conditions.

Geno NIPT 23 Pro

1 tests · Turnaround 2–4 days

Screens all 23 chromosome pairs and an additional 60 microdeletion/microduplication syndromes involving chromosomal copy-number variants (CNVs).

Geno NIPT 23 Ultra

1 tests · Turnaround 2–4 days

Screens all 23 chromosome pairs with expanded detection of 90 chromosomal microdeletion/microduplication syndromes.

Geno NIPT 3 Twins

1 tests · Turnaround 2–4 days

Screens for Down, Edwards and Patau syndromes, designed specifically for twin pregnancies.

Geno NIPT 23 Twins

1 tests · Turnaround 2–4 days

Screens chromosome number abnormalities across all 23 chromosome pairs for twin pregnancies.

Prenatal Care – First Trimester (11–13 weeks)

19 tests · Turnaround 1–2 days

Early, non-invasive screening for fetal chromosomal abnormalities from a single maternal blood draw, with high accuracy.

Prenatal Care – Second Trimester (16–18 weeks)

13 tests · Turnaround 1 hour

Early, non-invasive screening for fetal chromosomal abnormalities from a single maternal blood draw, with high accuracy.

Prenatal Care – 22 Weeks

13 tests · Turnaround 1–2 days

Early, non-invasive screening for fetal chromosomal abnormalities from a single maternal blood draw, with high accuracy.

Prenatal Care – 26 Weeks

12 tests · Turnaround 1 hour

Early, non-invasive screening for fetal chromosomal abnormalities from a single maternal blood draw, with high accuracy.

Prenatal Care – 32 Weeks

13 tests · Turnaround 1 hour

Early, non-invasive screening for fetal chromosomal abnormalities from a single maternal blood draw, with high accuracy.

Prenatal Care – 37 Weeks

14 tests · Turnaround 1 day

Early, non-invasive screening for fetal chromosomal abnormalities from a single maternal blood draw, with high accuracy.

Understanding NIPT screening

NIPT analyzes cell-free DNA in maternal blood, including DNA originating from the placenta, to assess the chance of selected fetal chromosome conditions. It uses a maternal blood sample without directly sampling the fetus. Packages differ in scope; choose after counseling, not simply by the number of items.

From blood sample to result counseling

Counseling & maternal blood sample
1

Counseling & maternal blood sample

Confirm gestational age, history and package suitability with your clinician before sampling.

DNA analysis
2

DNA analysis

The laboratory analyzes the sample within the chosen panel. Result turnaround: 2–4 days.

Results & follow-up counseling
3

Results & follow-up counseling

Your clinician explains the risk, the result’s limitations and any follow-up needed.

Cancer Screening

2 packages

General Health Check-up

2 packages

Pre-marital Screening

3 packages

Micronutrients & Nutrition

2 packages

Men's Health

1 packages