Clinical and research tests for 4635 - Genetic Testing Registry (GTR) - NCBI

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Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
GenepoweRx_Cardiac Care GenepoweRx Uppaluri K&H Personalized Medicine Clinic India	63	102	D Deletion/duplication analysis H Detection of homozygosity S Mutation scanning of the entire coding region T Targeted variant analysis
MYL4 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany	1	1	D Deletion/duplication analysis 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
Atrial fibrillation Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States	1	21	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Atrial fibrillation NGS panel HNL Genomics Connective Tissue Gene Tests United States	1	21	C Sequence analysis of the entire coding region T Targeted variant analysis
Atrial fibrillation Deletion/ Duplication panel HNL Genomics Connective Tissue Gene Tests United States	1	21	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Atrial fibrillation, familial, 18, 617280, Autosomal dominant (Familial atrial fibrillation) (MYL4 gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey	1	1	C Sequence analysis of the entire coding region
Comprehensive Cardiology Panel PreventionGenetics, part of Exact Sciences United States	223	198	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Atrial Fibrillation Syndrome via the MYL4 Gene PreventionGenetics, part of Exact Sciences United States	1	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Familial Atrial Fibrillation Syndrome Panel PreventionGenetics, part of Exact Sciences United States	16	20	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Invitae Arrhythmia and Cardiomyopathy Comprehensive Panel Invitae United States	239	100	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Invitae Arrhythmia Comprehensive Panel Invitae United States	115	41	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Comprehensive Cardiac Arrhythmia Panel PreventionGenetics, part of Exact Sciences United States	77	64	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Cardiovascular Comprehensive Panel CGC Genetics Unilabs Portugal	1	353	C Sequence analysis of the entire coding region
Cardiomyopathies Panel CGC Genetics Unilabs Portugal	1	197	C Sequence analysis of the entire coding region
Arrythmia Panel CGC Genetics Unilabs Portugal	1	79	C Sequence analysis of the entire coding region
Arrhythmia Panel Mendelics Brazil	1	311	C Sequence analysis of the entire coding region
Cardiomyopathy Panel Mendelics Brazil	1	311	C Sequence analysis of the entire coding region
Arrhythmia panel. NGS panel of 55 genes. Genologica Medica Spain	128	55	C Sequence analysis of the entire coding region
Genomic Unity® Custom Analysis Variantyx, Inc. United States	1	4054	D Deletion/duplication analysis X Mutation scanning of select exons 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.