Clinical and research tests for C2584774 - Genetic Testing Registry (GTR) - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

<< First < Prev

Page 2 of 3

Results: 21 to 40 of 42

Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
RenalZoom Johns Hopkins Genomics DNA Diagnostic Laboratory Johns Hopkins Hospital United States	527	338	C Sequence analysis of the entire coding region
Congenital Fibrinogen Deficiency via the FGB 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
Congenital Fibrinogen Deficiency via the FGG 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
Congenital Fibrinogen Deficiency Panel PreventionGenetics, part of Exact Sciences United States	1	3	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Congenital Fibrinogen Deficiency via the FGA 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
Invitae Hereditary Thrombophilia Panel Invitae United States	24	11	D Deletion/duplication analysis
Clotting factor deficiency panel. 16-gene NGS panel. Genologica Medica Spain	29	16	C Sequence analysis of the entire coding region
Familial Amyloidosis Genologica Medica Spain	44	19	C Sequence analysis of the entire coding region
Bleeding disorder / coagulopathy panel. NGS panel of 62 genes. Genologica Medica Spain	96	62	C Sequence analysis of the entire coding region
Afibrinogenemia, congenital: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada	1	3	C Sequence analysis of the entire coding region
Afibrinogenemia, congenital Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders Germany	1	2	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
Coagulation Disorders Asper Biogene Asper Biogene LLC Estonia	21	16	C Sequence analysis of the entire coding region
Congenital Fibrinogen Disorders , Panel Massive Sequencing (NGS) FGA, FGB, FGG Genes Reference Laboratory Genetics Spain	2	3	C Sequence analysis of the entire coding region
Bleeding Disorders , Panel Massive Sequencing (NGS) 23 Genes Reference Laboratory Genetics Spain	22	22	C Sequence analysis of the entire coding region
AFIBRINOGENEMIA – DYSFIBRINOGENEMIA – HYPOFIBRINOGENEMIA Laboratorio de Genetica Clinica SL Spain	2	3	C Sequence analysis of the entire coding region
Afibrinogenemia, congenital Labor Dr. Wisplinghoff Germany	1	3	C Sequence analysis of the entire coding region
Single gene testing FGA CeGaT GmbH Germany	3	1	C Sequence analysis of the entire coding region
Afibrinogenemia, congenital Bioarray Spain	1	1	C Sequence analysis of the entire coding region
Afibrinogenemia, congenital Bioarray Spain	1	1	C Sequence analysis of the entire coding region

<< First < Prev

Page 2 of 3

Results: 21 to 40 of 42

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.