• Ambry Genetics Announces One Millionth Test Leveraging RNA to Improve Diagnostic Accuracy and Yield

    Ambry Genetics Announces One Millionth Test Leveraging RNA to Improve Diagnostic Accuracy and Yield

    Milestone highlights growing adoption of DNA and RNA-informed diagnostics for hereditary cancer and rare disease

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  • <p>Ambry’s Contributions to MAVEs Support Thousands of Patient Reclassifications and Expand to New Genes</p>

    Ambry’s Contributions to MAVEs Support Thousands of Patient Reclassifications and Expand to New Genes

    Making Waves: New study published in Nature Communications builds on Ambry’s contributions to MAVE research to deepen understanding of PALB2 and its role in hereditary cancer predisposition.

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  • Ambry's Patient for Life™ Study Published in <em>Genetics in Medicine</em>

    Ambry's Patient for Life™ Study Published in Genetics in Medicine

    Peer-reviewed research highlights the power of proactive reanalysis in rare disease diagnosis.

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  • Genetic Clinicians and Rare Sibling Support

Dedicated to providing high-quality, accessible genetic testing

Your trusted laboratory for answers and innovation for nearly 25 years.

Accessible. Affordable. Actionable.

No qualified patient should go without necessary testing due to cost.

five patients

HISTORICALLY, 4 OUT OF 5 PATIENTS PAY

$0

one patient

AVERAGE COST FOR PATIENTS WHO DO PAY

(individual patient responsibility amounts may vary)

LESS THAN

$100

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Who We Are

With over 20 years of scientific innovations and discoveries, Ambry is an industry leader enabling healthcare professionals to confidently make informed care decisions with their patients by providing them with advanced genetic testing solutions.

At Ambry, people are at the center of our advancements, which starts with our own team. Recognized as an award-winning and outstanding place to work, we maintain a commitment to fostering diverse knowledge and perspectives to drive meaningful collaboration and help us all strive toward better health.

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