Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Cardiology Sequencing- Arrhythmia Comprehensive Panel (134 Genes) Genesys Diagnostics Genesys Diagnostics, Inc. United States | 88 | 134 |
|
Cardiology Sequencing- Full Panel (174 Genes) Genesys Diagnostics Genesys Diagnostics, Inc. United States | 122 | 174 |
|
CACNB2 Gene Brugada syndrome type 4 NGS Genetic DNA Test DNA Labs India India | 1 | 1 |
|
Comprehensive Arrhythmia Gene Panel Mayo Clinic Laboratories Mayo Clinic United States | 36 | 44 |
|
Cardiomyopathy and Arrhythmia Panel Mayo Clinic Laboratories Mayo Clinic United States | 73 | 105 |
|
GenepoweRx Uppaluri K&H Personalized Medicine Clinic India | 63 | 102 |
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CACNB2 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 1 | 1 |
|
Centogene AG - the Rare Disease Company Germany | 1886 | 1858 |
|
Centogene AG - the Rare Disease Company Germany | 777 | 770 |
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Centogene AG - the Rare Disease Company Germany | 289 | 275 |
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Centogene AG - the Rare Disease Company Germany | 829 | 848 |
|
Cardiac channelopathy Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States | 1 | 41 |
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Cardiac channelopathy NGS panel HNL Genomics Connective Tissue Gene Tests United States | 1 | 41 |
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Cardiac channelopathy Deletion/ Duplication panel HNL Genomics Connective Tissue Gene Tests United States | 1 | 41 |
|
Brugada syndrome and related disorders Deletion/ Duplication panel HNL Genomics Connective Tissue Gene Tests United States | 1 | 25 |
|
Brugada syndrome and related disorders Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States | 1 | 25 |
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Brugada syndrome and related disorders NGS panel HNL Genomics Connective Tissue Gene Tests United States | 1 | 25 |
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Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
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Labcorp Genetics (formerly Invitae) LabCorp United States | 409 | 164 |
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Labcorp Genetics (formerly Invitae) LabCorp United States | 208 | 81 |
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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.