Clinical and research tests for 609691 - Genetic Testing Registry (GTR) - NCBI

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Results: 1 to 16 of 16

Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
D-2-hydroxyglutaric aciduria (sequence analysis of D2HGDH gene) CGC Genetics Unilabs Portugal	1	1	C Sequence analysis of the entire coding region
Congenital Anomalies of the Gastrointestinal Tract Panel PreventionGenetics, part of Exact Sciences United States	297	180	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Pan Cardiomyopathy Panel PreventionGenetics, part of Exact Sciences United States	112	111	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Hypertrophic Cardiomyopathy Panel PreventionGenetics, part of Exact Sciences United States	67	64	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Comprehensive Cardiology Panel PreventionGenetics, part of Exact Sciences United States	224	202	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Cardiovascular panel _v.2.0 CGC Genetics Unilabs Portugal	1	264	C Sequence analysis of the entire coding region
Cardiomyopathy panel_v.2.0 CGC Genetics Unilabs Portugal	1	203	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
HYPERTROPHIC CARDIOMYOPATHY EXOME PANEL Laboratorio de Genetica Clinica SL Spain	1	197	E Sequence analysis of select exons
NON-COMPACTION CARDIOMYOPATHY EXOME PANEL Laboratorio de Genetica Clinica SL Spain	1	69	E Sequence analysis of select exons
SUDDEN DEATH/ IDIOPATHIC VENTRICULAR FIBRILLATION EXOME PANEL Laboratorio de Genetica Clinica SL Spain	1	394	E Sequence analysis of select exons
DILATED CARDIOMYOPATHY EXOME PANEL Laboratorio de Genetica Clinica SL Spain	1	141	E Sequence analysis of select exons
Cardiomyopathy, familial hypertrophic Panel by NGS Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute Canada	1	27	C Sequence analysis of the entire coding region T Targeted variant analysis
FHOD3 Single Gene Fulgent Genetics United States	1	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Hypertrophic Cardiomyopathy Genetics Laboratory University of Oklahoma Health Sciences Center United States	1	18	C Sequence analysis of the entire coding region

Results: 1 to 16 of 16

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.