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 |
|
Health in Code Spain | 1 | 218 |
|
Cardiovascular Diseases_General Panel Health in Code Spain | 1 | 380 |
|
Ventricular arrhythmia and sudden death without structural heart disease Health in Code Spain | 1 | 77 |
|
Long QT Syndrome Extended Panel Health in Code Spain | 1 | 28 |
|
Ventricular Arrythmia & Sudden Death Panel without Structural Heart Disease Health in Code Spain | 1 | 53 |
|
Ventricular Arrythmia & Sudden Death Panel with Structural Heart Disease Health in Code Spain | 1 | 141 |
|
Inherited Cardiovascular Diseases and Sudden Death Panel Health in Code Spain | 1 | 213 |
|
Long QT Syndrome Extended Panel Health in Code Spain | 1 | 23 |
|
Long QT syndrome (WES based NGS panel of 18 genes, including CNV analysis) CGC Genetics Unilabs Portugal | 1 | 18 |
|
Cardiac conduction changes (WES based NGS panel of 29 genes, including CNV analysis) CGC Genetics Unilabs Portugal | 1 | 29 |
|
SUDDEN DEATH/ IDIOPATHIC VENTRICULAR FIBRILLATION EXOME PANEL Laboratorio de Genetica Clinica SL Spain | 1 | 394 |
|
HEREDITARY ARRHYTHMIA EXOME PANEL Laboratorio de Genetica Clinica SL Spain | 1 | 160 |
|
Long QT Syndrome: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 19 | 16 |
|
GenepoweRx Uppaluri K&H Personalized Medicine Clinic India | 63 | 102 |
|
Centogene AG - the Rare Disease Company Germany | 289 | 275 |
|
PreventionGenetics, part of Exact Sciences United States | 22 | 19 |
|
Cardiac channelopathy Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States | 1 | 41 |
|
Cardiac channelopathy NGS panel HNL Genomics Connective Tissue Gene Tests United States | 1 | 41 |
|
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.