Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Personalis, Inc. United States | 1 | 413 |
|
Tempus AI - RTP United States | 2 | 647 |
|
Mayo Clinic Laboratories Mayo Clinic United States | 1 | 51 |
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Motor Neuron Disease Gene Panel Mayo Clinic Laboratories Mayo Clinic United States | 2 | 34 |
|
Tempus AI - CHI United States | 2 | 647 |
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Foundation Medicine, Inc. United States | 2 | 405 |
|
OnkoSight Advanced Breast Cancer Panel BioReference Health United States | 1 | 50 |
|
Comprehensive HemeComplete Profile + Heme Fusion + CALR PCR + FLT3 PCR PathGroup United States | 16 | 160 |
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Centogene AG - the Rare Disease Company Germany | 218 | 135 |
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ERBB4 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 1 | 1 |
|
Centogene AG - the Rare Disease Company Germany | 1886 | 1858 |
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Amyotrophic Lateral Sclerosis (ALS) / Dementia Panel Centogene AG - the Rare Disease Company Germany | 64 | 66 |
|
MayoComplete Solid Tumor Panel Mayo Clinic Laboratories Mayo Clinic United States | 1 | 476 |
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The Jackson Laboratory for Genomic Medicine United States | 1 | 517 |
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PathGroup United States | 73 | 505 |
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OmniSeq, Inc. United States | 1 | 525 |
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Labcorp Genetics (formerly Invitae) LabCorp United States | 72 | 33 |
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Amyotrophic lateral sclerosis and related disorders NGS panel HNL Genomics Connective Tissue Gene Tests United States | 1 | 24 |
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Amyotrophic lateral sclerosis and related disorders Deletion/ Duplication panel HNL Genomics Connective Tissue Gene Tests United States | 1 | 24 |
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Amyotrophic lateral sclerosis and related disorders Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States | 1 | 24 |
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IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.