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

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Results: 21 to 40 of 58

Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
Fibrinogen gene analysis (FGA, FGB & FGG) Molecular Haemostasis & Thrombosis Synnovis Analytics LLP - Guy's and St. Thomas' NHS Foundation Trust United Kingdom	3	3	C Sequence analysis of the entire coding region
Bleeding Disorders Panel PreventionGenetics, part of Exact Sciences United States	78	79	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Coagulation Factor Deficiency Panel PreventionGenetics, part of Exact Sciences United States	21	20	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Hematology Comprehensive Panel CGC Genetics Unilabs Portugal	1	291	C Sequence analysis of the entire coding region
Bleeding Disorders Panel CGC Genetics Unilabs Portugal	1	121	C Sequence analysis of the entire coding region
Afibrinogenemia, congenital , Dysfibrinogenemia, congenital , Hypofibrinogenemia, congenital (sequence analysis of FGB gene) CGC Genetics Unilabs Portugal	1	1	C Sequence analysis of the entire coding region
Coagulation Disorders Panel Mendelics Brazil	1	51	C Sequence analysis of the entire coding region
Clotting factor deficiency panel. 16-gene NGS panel. Genologica Medica Spain	29	16	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
Fibrinogen Disorders Panel Versiti Diagnostic Laboratories Versiti, Inc United States	1	3	D Deletion/duplication analysis 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
Afibrinogenemia familiar Bioarray Spain	1	2	C Sequence analysis of the entire coding region
Genomic Unity® Custom Analysis Variantyx, Inc. United States	1	4054	D Deletion/duplication analysis X Mutation scanning of select exons 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
Xpanded Adult Movement Disorders Panel GeneDx United States	5	473	C Sequence analysis of the entire coding region
Fibrinogen Genetic Analysis MNG Laboratories (Medical Neurogenetics, LLC.) United States	1	3	C Sequence analysis of the entire coding region
Platelet Function Genetic Analysis MNG Laboratories (Medical Neurogenetics, LLC.) United States	3	31	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
NewbornDx Advanced Sequencing Evaluation Athena Diagnostics United States	1	1722	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.

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Results: 21 to 40 of 58

Results: 21 to 40 of 58