Filters
reset allTests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Cardiomyopathy and Arrhythmia Panel Mayo Clinic Laboratories Mayo Clinic United States | 73 | 105 |
|
Comprehensive Cardiomyopathy Panel Mayo Clinic Laboratories Mayo Clinic United States | 68 | 83 |
|
Congenital Heart Disease Gene Panel Mayo Clinic Laboratories Mayo Clinic United States | 22 | 44 |
|
Hypertrophic Cardiomyopathy Panel Mayo Clinic Laboratories Mayo Clinic United States | 44 | 48 |
|
Dilated Cardiomyopathy/LVNC Panel Mayo Clinic Laboratories Mayo Clinic United States | 52 | 63 |
|
Noonan Syndrome and Related Panel Mayo Clinic Laboratories Mayo Clinic United States | 15 | 20 |
|
UAB Medical Genomics Laboratory UAB Medicine United States | 8 | 18 |
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UAB Medical Genomics Laboratory UAB Medicine United States | 7 | 17 |
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Clinical Genomics Unit Hospital Universitari Germans Trias i Pujol Spain | 5 | 16 |
|
Clinical Genomics Unit Hospital Universitari Germans Trias i Pujol Spain | 9 | 19 |
|
Centogene AG - the Rare Disease Company Germany | 740 | 728 |
|
PGmax™ - Comprehensive Congenital Heart Disease Panel PreventionGenetics, part of Exact Sciences United States | 24 | 1 |
|
Noonan syndrome core Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States | 10 | 14 |
|
Noonan syndrome core Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests United States | 10 | 14 |
|
GeneSeq® Cardio Single Gene Analysis Integrated Genetics Westborough LabCorp United States | 55 | 177 |
|
GeneSeq® Cardio: Noonan Syndrome/RASopathies Panel Integrated Genetics Westborough LabCorp United States | 6 | 20 |
|
Noonan Syndrome, Fetal Analysis Integrated Genetics Westborough LabCorp United States | 5 | 19 |
|
Noonan and Comprehensive RASopathies Panel GeneDx United States | 2 | 25 |
|
Combined Cardiac Sequencing and Del/Dup Panel GeneDx United States | 10 | 138 |
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Comprehensive Primary Immunodeficiency NGS Panel Fulgent Genetics United States | 1048 | 472 |
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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.