Clinical and research tests for C4707243 - 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
Connective tissue disorder NGS panel HNL Genomics Connective Tissue Gene Tests United States	37	47	C Sequence analysis of the entire coding region T Targeted variant analysis
Connective tissue disorder Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States	37	47	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	223	198	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Ehlers-Danlos Syndromes (EDS) Panel PreventionGenetics, part of Exact Sciences United States	99	65	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Targeted Variant Analysis Integrated Genetics Westborough LabCorp United States	330	746	T Targeted variant analysis
TGFBR1 Gene, entire coding region or targeted variant Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute Canada	2	1	C Sequence analysis of the entire coding region T Targeted variant analysis
TGFBR2 Gene, entire coding region or targeted variant Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute Canada	2	1	C Sequence analysis of the entire coding region T Targeted variant analysis
FBN1 Gene, entire coding region or targeted variant Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute Canada	2	1	C Sequence analysis of the entire coding region T Targeted variant analysis
MYLK Gene, entire coding region or targeted variant Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute Canada	1	1	C Sequence analysis of the entire coding region T Targeted variant analysis
MYH11 Gene, entire coding region or targeted variant Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute Canada	1	1	C Sequence analysis of the entire coding region T Targeted variant analysis
SLC2A10 Gene, entire coding region or targeted variant Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute Canada	1	1	C Sequence analysis of the entire coding region T Targeted variant analysis
TGFB2 Gene, entire coding region or targeted variant Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute Canada	2	1	C Sequence analysis of the entire coding region T Targeted variant analysis
TGFB3 Gene, entire coding region or targeted variant Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute Canada	3	1	C Sequence analysis of the entire coding region T Targeted variant analysis
SMAD3 Gene, entire coding region or targeted variant Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute Canada	2	1	C Sequence analysis of the entire coding region T Targeted variant analysis
ACTA2 Gene, entire coding region or targeted variant Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute Canada	1	1	C Sequence analysis of the entire coding region T Targeted variant analysis
Aortic Aneurysm, Familial Thoracic Panel by NGS Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute Canada	1	10	C Sequence analysis of the entire coding region T Targeted variant analysis

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.