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| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Brugada syndrome and related disorders Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests United States | 18 | 26 |
|
PreventionGenetics, part of Exact Sciences United States | 63 | 49 |
|
Comprehensive Cardiology Panel PreventionGenetics, part of Exact Sciences United States | 223 | 198 |
|
PreventionGenetics, part of Exact Sciences United States | 5 | 7 |
|
Comprehensive Cardiac Arrhythmia Panel PreventionGenetics, part of Exact Sciences United States | 77 | 64 |
|
PreventionGenetics, part of Exact Sciences United States | 9 | 17 |
|
Brugada Syndrome via the CACNB2 Gene PreventionGenetics, part of Exact Sciences United States | 1 | 1 |
|
Arrhythmia panel. NGS panel of 55 genes. Genologica Medica Spain | 128 | 55 |
|
Atrial fibrillation panel. NGS panel of 19 genes. Genologica Medica Spain | 55 | 19 |
|
Genologica Medica Spain | 12 | 5 |
|
Brugada syndrome panel. 9-gene NGS panel. Genologica Medica Spain | 26 | 9 |
|
CNH Molecular Diagnostics Laboratory Childrens National Hospital United States | 25 | 14 |
|
Arrhythmia & Cardiomyopathy Panel, Comprehensive CNH Molecular Diagnostics Laboratory Childrens National Hospital United States | 211 | 93 |
|
Arrhythmia Panel, Comprehensive CNH Molecular Diagnostics Laboratory Childrens National Hospital United States | 71 | 36 |
|
Institute for Human Genetics University Medical Center Freiburg Germany | 1 | 1 |
|
Comprehensive Cardiomyopathy NGS Panel Fulgent Genetics United States | 450 | 128 |
|
Long QT/Brugada Syndrome NGS Panel Fulgent Genetics United States | 69 | 34 |
|
Arrhythmogenic Right Ventricular Cardiomyopathy NGS Panel Fulgent Genetics United States | 118 | 46 |
|
Brugada Syndrome: gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 11 | 9 |
|
Cardiology Genetic Panel (Full) , Panel Massive Sequencing (NGS) 96 Genes Reference Laboratory Genetics Spain | 119 | 95 |
|
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.