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For Geneticists and Genetic Counselors

Precision genetic insights for geneticists and 
‍genetic counselors

Expert-level clinical guidance and genomic insights powered by the industry’s largest rare disease dataset.
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Explore how GeneDx supports geneticists and genetic counselors with comprehensive genomic testing and expert resources.

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Built for clinical action

Trusted answers for genetics experts

High-quality precision
Precise interpretation informed by the Infinity™ rare disease dataset, built from more than 2.5 million genetic tests enriched for rare disease and over 8 million phenotypic datapoints.
Clearer results, better guidance
Cleaner reports and fewer VUS calls support confident clinical decision-making and clearer next steps in care.
Easily accessible
Fast turnaround times, within days or weeks, paired with broad insurance coverage and Medicaid participation in 38 states.
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Scale that drives clinical confidence

  • 2.5M+ genetic tests inform variant classification
  • Over 10.5K curated gene-disease associations
  • ~50% of the Infinity dataset is derived from non-European populations, advancingequity
  • #1 ranked genomic testing brand among pediatric and genetic physicians
  • Results delivered in days to weeks
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One approach.
Two powerful options

When compared to other tests, exome and genome sequencing are more likely to deliver a genetic diagnosis. In fact, 23% of patients diagnosed via exome testing would not have received a diagnosis with a genetic testing panel.

ExomeDx™

Our standard exome sequencing option for patients with suspected genetic conditions, developmental delay, congenital anomalies, epilepsy, or multisystem involvement.

Available for proband, duo, or trio.

Mito analysis can be added as an option.

Results as soon as 2 weeks*

GenomeDx™

Our standard genome sequencing option for routine or complex cases where comprehensive detection is preferred.

Available for proband, duo, or trio.

Results as soon as 4 weeks*

GeneDx also offers a comprehensive menu of targeted variant testing options for families who had previous testing at GeneDx as well as for families who had prior testing at another laboratory. Learn more about targeted variant testing for familial variants.

Broad clinical application

Select one to learn more.

Developmental delay and intellectual disability
Epilepsy
Autism
Cerebral Palsy

Supported by one of the largest genomic databases

With one of the most comprehensive and diverse genomic databases in the industry, GeneDx Infinity delivers insights powered by over a million sequenced exomes and genomes.

Our unmatched scale and expertise ensure every result is informed by deep data, diverse representation, and decades of clinical experience—offering more than a test result, but a clearer path to diagnosis.

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How to Order

Ordering is simple, and GeneDx integrates seamlessly into your existing workflow. Providers using Epic Aura can place orders directly within their system. 

Learn more about ordering
1

Choose a test

Search the test catalog by gene, condition, or indication to identify the most appropriate test for each patient.

2

Submit a sample

Request a collection kit, collect the sample, and ship it using the provided materials and instructions.

3

Receive results

Results are delivered securely through the GeneDx ordering portal with clear findings, interpretation, and clinical guidance.

Clinical support for geneticists and genetic counselors

When you have complex clinical questions, you need timely, reliable answers. Our team of experts supports you throughout the entire testing process.

Pre-order guidance
Test selection, insurance criteria, and case review
Mid-process assistance
Sample adequacy, billing questions, and consent logistics
Post-result interpretation
Clear, actionable guidance for patient management
Connect with our clinical support team
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Real cases, real clarity

Meet Savannah

“There was an ounce of relief in [getting the diagnosis], because we had been waiting for answers and now we had them. We now had some sort of direction, too.” —Emily, Savannah's mother

Meet Sarah

Sarah had no specific cardiac symptoms at birth but was diagnosed with a CHD after concerns were first identified via a routine visit to her pediatrician. After a year-long wait for a genetics evaluation, she received a genetic diagnosis.

Resources & events

Data insights

Infinity dataset overview

Finding

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Ordering

Test ordering workflow guides

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Webinar

Webinars and educational presentations for clinical genetics

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Ready to bring genomics into your practice?

We’re here to support every step.