Clinical and research tests for C1960469 - Genetic Testing Registry (GTR) - NCBI

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Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
Comprehensive Arrhythmia Gene Panel Mayo Clinic Laboratories Mayo Clinic United States	36	44	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Arrhythmogenic Cardiomyopathy Panel Mayo Clinic Laboratories Mayo Clinic United States	26	18	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Cardiomyopathy and Arrhythmia Panel Mayo Clinic Laboratories Mayo Clinic United States	73	105	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Comprehensive Cardiomyopathy Panel Mayo Clinic Laboratories Mayo Clinic United States	68	83	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Hypertrophic Cardiomyopathy Panel Mayo Clinic Laboratories Mayo Clinic United States	44	48	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Dilated Cardiomyopathy/LVNC Panel Mayo Clinic Laboratories Mayo Clinic United States	52	63	D Deletion/duplication analysis 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
Cardiac Diseases Gene panel Clinical Genomics Laboratory Washington University in St. Louis United States	12	150	C Sequence analysis of the entire coding region
MYH7 Sequencing Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center United States	4	1	S Mutation scanning of the entire coding region
MYBPC3 Sequencing Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center United States	4	1	S Mutation scanning of the entire coding region
Comprehensive Cardiomyopathy Panel (37 genes) Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center United States	4	37	X Mutation scanning of select exons S Mutation scanning of the entire coding region
Hypertrophic Cardiomyopathy Panel, Sequencing ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories United States	25	34	C Sequence analysis of the entire coding region
Comprehensive Cardiomyopathy NGS Panel Fulgent Genetics United States	450	128	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Cardiomyopathy Panel Blueprint Genetics Finland	6	155	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Comprehensive Cardiology Panel Blueprint Genetics Finland	12	185	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Left Ventricular Non-Compaction Cardiomyopathy (LVNC) Panel Blueprint Genetics Finland	1	32	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Non-Compaction Arrhythmogenic Left Ventricular Cardiomyopathy Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University United States	5	12	C Sequence analysis of the entire coding region
PRDM16 Single Gene Fulgent Genetics United States	13	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region
MIB1 Single Gene Fulgent Genetics United States	4	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Left Ventricular Noncompaction Cardiomyopathy (LVNC) Panel CeGaT GmbH Germany	8	11	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.