Clinical and research tests for C5703318 - Genetic Testing Registry (GTR) - NCBI

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Results: 1 to 19 of 19

Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
von Willebrand Disease, VWF Gene, Full Gene Next-Generation Sequencing Mayo Clinic Laboratories Mayo Clinic United States	1	1	C Sequence analysis of the entire coding region
von Willebrand Disease Gene Sequencing Quest Diagnostics Nichols Institute San Juan Capistrano United States	1	1	C Sequence analysis of the entire coding region
DNA von Willebrand Disease Evaluation Bloodworks Genomics - Bleeding Disorders BloodworksNW United States	1	1	E Sequence analysis of select exons
von Willebrand Disease (VWF) Sequencing ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories United States	1	1	C Sequence analysis of the entire coding region
Von Willebrand Disease Genetiks Genetic Diagnosis Center Genetic Diseases Evaluation Center Turkey	1	1	C Sequence analysis of the entire coding region
Comprehensive Bleeding Disorder Panel Versiti Diagnostic Laboratories Versiti, Inc United States	80	50	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Thrombocytopenia Genetic Analysis MNG Laboratories (Medical Neurogenetics, LLC.) United States	20	26	C Sequence analysis of the entire coding region
von Willebrand Disease Genetic Analysis MNG Laboratories (Medical Neurogenetics, LLC.) United States	1	2	C Sequence analysis of the entire coding region
Coagulation Disorder Panel Versiti Diagnostic Laboratories Versiti, Inc United States	25	20	D Deletion/duplication analysis S Mutation scanning of the entire coding region
von Willebrand Disease: gene deletion/duplication CEN4GEN Institute for Genomics and Molecular Diagnostics Canada	1	1	D Deletion/duplication analysis
von Willebrand Disease: gene sequencing CEN4GEN Institute for Genomics and Molecular Diagnostics Canada	1	1	C Sequence analysis of the entire coding region
VON WILLEBRAND DISEASE Laboratorio de Genetica Clinica SL Spain	1	1	E Sequence analysis of select exons C Sequence analysis of the entire coding region
Coagulation Factor Deficiency Panel Blueprint Genetics Finland	3	16	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Platelet Disorders Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University United States	12	55	C Sequence analysis of the entire coding region
Von Willebrand disease, VWF sequencing Molecular Diagnostics Laboratory Seoul National University Hospital South Korea	1	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region
VWF Exon 28 Sequence Analysis (For Type 2M or 2B VWD) Versiti Diagnostic Laboratories Versiti, Inc United States	2	1	E Sequence analysis of select exons
VWF Sequence Analysis (All Exons) Versiti Diagnostic Laboratories Versiti, Inc United States	8	1	C Sequence analysis of the entire coding region
von Willebrand Disease (VWF) MVZ Dr. Eberhard & Partner Dortmund Germany	8	1	D Deletion/duplication analysis E Sequence analysis of select exons C Sequence analysis of the entire coding region
von Willebrand Disease Diagenom GmbH Germany	1	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region

Results: 1 to 19 of 19

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.