Clinical and research tests for 505219 - Genetic Testing Registry (GTR) - NCBI

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Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
Hypertrophic Cardiomyopathy panel Clinical Genomics Laboratory Washington University in St. Louis United States	1	42	C Sequence analysis of the entire coding region
Dilated Cardiomyopathy panel Clinical Genomics Laboratory Washington University in St. Louis United States	1	68	C Sequence analysis of the entire coding region
Arrhythmogenic Right Ventricular Cardiomyopathy panel Clinical Genomics Laboratory Washington University in St. Louis United States	1	17	C Sequence analysis of the entire coding region
Cardiomyopathy panel Clinical Genomics Laboratory Washington University in St. Louis United States	5	96	C Sequence analysis of the entire coding region
Long QT Syndromes panel Clinical Genomics Laboratory Washington University in St. Louis United States	2	16	C Sequence analysis of the entire coding region
Catecholaminergic Polymorphic Ventricular Tachycardia panel Clinical Genomics Laboratory Washington University in St. Louis United States	2	7	C Sequence analysis of the entire coding region
Brugada Syndromes panel Clinical Genomics Laboratory Washington University in St. Louis United States	2	17	C Sequence analysis of the entire coding region
Cardiac Diseases Gene panel Clinical Genomics Laboratory Washington University in St. Louis United States	12	150	C Sequence analysis of the entire coding region
Whole Exome Sequencing Clinical Genomics Laboratory Washington University in St. Louis United States	1	1	C Sequence analysis of the entire coding region
Somatic Undergrowth Panel with interpretation Clinical Genomics Laboratory Washington University in St. Louis United States	5	6	C Sequence analysis of the entire coding region
Rasopathies panel with interpretation Clinical Genomics Laboratory Washington University in St. Louis United States	1	26	C Sequence analysis of the entire coding region
Inborn Errors of Immunity Panel with interpretation Clinical Genomics Laboratory Washington University in St. Louis United States	8	9	C Sequence analysis of the entire coding region
Cortical Malformations and Epilepsy Panel with interpretation Clinical Genomics Laboratory Washington University in St. Louis United States	35	39	C Sequence analysis of the entire coding region
Vascular Anomalies Panel with interpretation Clinical Genomics Laboratory Washington University in St. Louis United States	1	65	C Sequence analysis of the entire coding region
Monogenic Diabetes and MODY Panel Clinical Genomics Laboratory Washington University in St. Louis United States	1	44	C Sequence analysis of the entire coding region
Permanent Neonatal Diabetes Mellitus (PNDM) Panel Clinical Genomics Laboratory Washington University in St. Louis United States	1	29	C Sequence analysis of the entire coding region
Hyperinsulinism Panel Clinical Genomics Laboratory Washington University in St. Louis United States	4	18	C Sequence analysis of the entire coding region
Endoplasmic Reticulum (ER) Stress Disorders Panel Clinical Genomics Laboratory Washington University in St. Louis United States	1	5	C Sequence analysis of the entire coding region
Atypical Diabetes and ER Stress Disorders Gene Panel Clinical Genomics Laboratory Washington University in St. Louis United States	1	54	C Sequence analysis of the entire coding region
Cystic Disease and Nephronopthisis panel Clinical Genomics Laboratory Washington University in St. Louis United States	16	33	C Sequence analysis of the entire coding region

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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.