Clinical and research tests for C0949658 - 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
Hypertrophic cardiomyopathy extended panel Health in Code Spain	1	104	C Sequence analysis of the entire coding region
Hypertrophic cardiomyopathy panel Health in Code Spain	1	17	C Sequence analysis of the entire coding region
Hypertrophic cardiomyopathy with suspected Noonan Syndrome Health in Code Spain	1	2	C Sequence analysis of the entire coding region
Hypertrophic cardiomyopathy with suspeced Fabry disease Health in Code Spain	1	1	C Sequence analysis of the entire coding region
Hypertrophic cardiomyopathy wiht suspected familial amyloidosis Health in Code Spain	1	1	C Sequence analysis of the entire coding region
Hypertrophic cardiomyopathy associated with pre-exctiation, WPW sndrome and/or conduction disorders Health in Code Spain	1	2	C Sequence analysis of the entire coding region
Standard hypertrophic cardiomyopathy Stage 2 Health in Code Spain	1	4	C Sequence analysis of the entire coding region
Standard hypertrophic cardiomyopathy Stage 1 Health in Code Spain	1	5	C Sequence analysis of the entire coding region
CentoCardio Panel Centogene AG - the Rare Disease Company Germany	289	275	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Hereditary Heart Health Test Color Diagnostics, LLC DBA Color Health United States	19	30	C Sequence analysis of the entire coding region
Cardiomyopathy Exome Panel Northwest Clinical Genomics Laboratory University Of Washington United States	32	75	C Sequence analysis of the entire coding region
Hereditary Disease Risk Test Color Diagnostics, LLC DBA Color Health United States	51	59	C Sequence analysis 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
Congenital muscular dystrophy Asper Biogene Asper Biogene LLC Estonia	59	28	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.