Clarity in the moments that matter most
Every report we create is powered by GeneDx Infinity, the largest rare disease and prenatal exome dataset.1
- ~1M exomes & genomes sequenced
- 4K+ prenatal exomes sequenced
- 2.5M+ tests
- 7M+ phenotypes
The right genetic test can change everything
Our suite of prenatal tests helps you uncover answers with precision and speed without needing to work with multiple labs or collect multiple samples.
GenomeDx™ Prenatal
Use when: Complex or unexplained fetal anomalies are detected via ultrasound and CMA and karyotype are non-diagnostic, and comprehensive genomic analysis is needed.*
*GenomeDx Prenatal is currently not available in New York State.
#1 genetic test
Trusted by over 75,000 healthcare providers.1
*Incremental diagnostic yield
*Incremental diagnostic yield
Specimen requirements
We accept amniotic fluid, cultured amniocytes, cultured chorionic villi (CVS), products of conception (POC), and extracted DNA. A maternal blood or buccal sample is required to conduct maternal cell contamination (MCC) studies. A paternal and maternal blood or buccal sample is also required for exome/genome trio, chromosomal microarray (CMA), and panel tests.
Reflex to exome with the same sample
We accept amniotic fluid, cultured amniocytes, cultured chorionic villi (CVS), products of conception (POC), and extracted DNA. A maternal blood or buccal sample is required to conduct maternal cell contamination (MCC) studies. A paternal and maternal b
When CMA or panel testing does not provide an answer, automatically reflex to exome using the same sample with no additional ordering steps or sample requirements, and faster access to clinically actionable insights.2
- No need to collect another sample
- No need to create a new order
- No delay in care
Covered for more patients than you think
We accept all commercial insurance plans, Medicaid, Medicare, and TRICARE. Our dedicated billing team helps secure the best coverage for your patients, and we offer competitive self-pay pricing, interest-free payment plans, and a Financial Assistance Program for eligible families.
Learn more about our coverage and patient support.
A diverse set of indications
Prenatal genetic testing can uncover the genetic cause or disease behind the following anomalies and many more:
"To me, nothing is more important than the reporting so that you can make sure you're giving your patients the highest quality and the best variant interpretation. This is where GeneDx really stands up and does an excellent job"
Start with exome when time is limited
Many providers start with CMA or panels, and those are still critical tools. But when ultrasound findings raise concern and time is limited, going straight to exome can save families weeks of waiting with stepwise testing.
