Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Cardiomyopathy and Arrhythmia Panel, Sequencing and Deletion/Duplication ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories United States | 125 | 83 |
|
MVZ Dr. Eberhard & Partner Dortmund Germany | 1 | 1 |
|
Cardio-channelopathy-gene-panel MVZ Dr. Eberhard & Partner Dortmund Germany | 35 | 33 |
|
MVZ Dr. Eberhard & Partner Dortmund Germany | 1 | 1 |
|
Fulgent Genetics United States | 2 | 1 |
|
Left Ventricular Non-Compaction Cardiomyopathy NGS Panel Fulgent Genetics United States | 82 | 24 |
|
Invitae Brugada Syndrome Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 7 | 8 |
|
Fulgent Genetics United States | 5128 | 4672 |
|
Cardiac Arrhythmia NGS Multi-Gene Panel (48 genes), Sequence & CNV analysis Amsterdam UMC Genome Diagnostics Amsterdam University Medical Center Netherlands | 7 | 47 |
|
Cardiac conduction abnormalities panel Genome Diagnostics Laboratory University Medical Center Utrecht Netherlands | 76 | 33 |
|
Fulgent Genetics United States | 84 | 24 |
|
Comprehensive Cardiovascular NGS Panel Fulgent Genetics United States | 671 | 250 |
|
Comprehensive Arrhythmia NGS Panel Fulgent Genetics United States | 184 | 76 |
|
John Welsh Cardiovascular Diagnostic Laboratory Baylor College of Medicine United States | 1 | 1 |
|
Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center United States | 100 | 73 |
|
Left Ventricular Noncompaction Panel Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center United States | 51 | 36 |
|
Cardiomyopathy NGS Multi-Gene Panel (50 genes), Sequence & CNV analysis Amsterdam UMC Genome Diagnostics Amsterdam University Medical Center Netherlands | 5 | 51 |
|
Amsterdam UMC Genome Diagnostics Amsterdam University Medical Center Netherlands | 1 | 1 |
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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.