Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Comprehensive Cardiology Panel PreventionGenetics, part of Exact Sciences United States | 224 | 202 |
|
Cardiac Arrhythmia Exome Panel Northwest Clinical Genomics Laboratory University of Washington United States | 39 | 51 |
|
Comprehensive Cardiac Arrhythmia Panel PreventionGenetics, part of Exact Sciences United States | 79 | 65 |
|
Long QT Syndrome via the KCNJ5 Gene PreventionGenetics, part of Exact Sciences United States | 1 | 1 |
|
GeneSeq® Neuro: Hypokalemic and Hyperkalemic Periodic Paralysis Panel MNG Laboratories (Medical Neurogenetics, LLC.) United States | 6 | 5 |
|
Long QT syndrome 13 (sequence analysis of KCNJ5 gene) CGC Genetics Unilabs Portugal | 1 | 1 |
|
Inherited Cadiac Disorders Panel Dhiti Omics Technologies Private Ltd India | 60 | 33 |
|
Arrhythmia panel. NGS panel of 55 genes. Genologica Medica Spain | 128 | 55 |
|
Long QT syndrome panel. 16-gene NGS panel. Genologica Medica Spain | 36 | 16 |
|
Atrial fibrillation panel. NGS panel of 19 genes. Genologica Medica Spain | 55 | 19 |
|
Pseudohypoaldosterolism panel. NGS panel of 10 genes. Genologica Medica Spain | 15 | 10 |
|
Monogenic Hypertension Genetic Panel MNG Laboratories (Medical Neurogenetics, LLC.) United States | 16 | 11 |
|
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 |
|
CNH Molecular Diagnostics Laboratory Childrens National Hospital United States | 34 | 15 |
|
Institute for Human Genetics University Medical Center Freiburg Germany | 2 | 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 |
|
Long QT Syndrome: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 18 | 16 |
|
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.