Clinical and research tests for 9421 - Genetic Testing Registry (GTR) - NCBI

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Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
Nonsyndromic Congenital Heart Disease Panel PreventionGenetics, part of Exact Sciences United States	54	44	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Invitae Congenital Heart Disease Panel Labcorp Genetics (formerly Invitae) LabCorp United States	107	55	D Deletion/duplication analysis 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
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
GeneSeq Cardio Targeted Variant Analysis Integrated Genetics Westborough LabCorp United States	55	177	T Targeted variant analysis
GeneSeq® Cardio Single Gene Analysis Integrated Genetics Westborough LabCorp United States	55	177	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Congenital Heart Defects Panel CGC Genetics Unilabs Portugal	1	208	C Sequence analysis of the entire coding region
Targeted Variant, Fetal Analysis Integrated Genetics Westborough LabCorp United States	292	746	T Targeted variant analysis
Partner Reflex to GeneSeq Integrated Genetics Westborough LabCorp United States	330	746	C Sequence analysis of the entire coding region
GeneSeq® Cardio: Familial Congenital Heart Disease Panel Integrated Genetics Westborough LabCorp United States	8	17	D Deletion/duplication analysis 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
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
Congenital structural heart disease panel. NGS panel of 62 genes. Genologica Medica Spain	113	62	C Sequence analysis of the entire coding region
Congenital Heart Defect NGS Panel Fulgent Genetics United States	377	114	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
Congenital Structural Heart Disease Panel Blueprint Genetics Finland	9	62	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Dilated Cardiomyopathy (DCM) Panel Blueprint Genetics Finland	1	70	D Deletion/duplication analysis 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.