Dedicated to providing high-quality, accessible genetic testing

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

Hereditary Cancer

Paired DNA/RNA testing with +RNAinsight® analyzes functional RNA data to help detect and classify DNA variants. This approach identifies more positive results, resolves variants of uncertain significance, and reduce evidence gaps in non-White populations.

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Rare Disease

Exome testing through Ambry Genetics includes proactive reanalysis through our Patient for Life program. This premium service provides updated exome testing findings as new gene-disease discoveries are validated, at no additional cost to the patient.

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Patient Education & Identification

The Ambry CARE Program® is a unique, end-to-end digital health solution designed to identify patients at increased risk for certain health conditions who may qualify for genetic testing, provide patient education, and facilitate test ordering and result reporting. CARE supports proactive, patient-centric healthcare while enabling practice productivity.

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What We're Up To
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Delivering
Accuracy

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Bringing
Clarity

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Advancing
Science

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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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