Clinical and research tests for C0272317 - Genetic Testing Registry (GTR)

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Results: 21 to 40 of 44

Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
Factor II (prothrombin) mutation analysis 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
Female Infertility Asper Biogene Asper Biogene LLC Estonia	85	64	C Sequence analysis of the entire coding region
Super Panel Plus NxGen MDx United States	116	117	D Deletion/duplication analysis E Sequence analysis of select exons C Sequence analysis of the entire coding region T Targeted variant analysis
Factor II and Factor V Leiden Panel NxGen MDx United States	6	6	D Deletion/duplication analysis E Sequence analysis of select exons C Sequence analysis of the entire coding region
Universal Panel Plus NxGen MDx United States	21	22	D Deletion/duplication analysis E Sequence analysis of select exons C Sequence analysis of the entire coding region T Targeted variant analysis
Coagulation Disorder Panel Versiti Diagnostic Laboratories Versiti, Inc United States	25	20	D Deletion/duplication analysis S Mutation scanning of the entire coding region
Thrombosis Disorder NGS Panel Fulgent Genetics United States	46	18	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Comprehensive Thrombosis, Platelet Disorder, and Coagulation Deficiency NGS Panel Fulgent Genetics United States	146	82	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Beacon Expanded Female Carrier Screening Plus Panel Fulgent Genetics United States	716	335	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Beacon Expanded Male Carrier Screening Plus Panel Fulgent Genetics United States	661	306	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
Prothrombin polymorphism in thrombophilia Genetics Service Unit National Institute of Biomedical Genomics India	1	1	T Targeted variant analysis
Bleeding Disorders , Panel Massive Sequencing (NGS) 23 Genes Reference Laboratory Genetics Spain	22	22	C Sequence analysis of the entire coding region
Single gene testing F2 CeGaT GmbH Germany	2	1	C Sequence analysis of the entire coding region
Factor II mutation study Diagnostics Division CENTRE FOR DNA FINGERPRINTING AND DIAGNOSTICS India	1	1	E Sequence analysis of select exons
Thrombophilia Centre for cellular and molecular biology Centre for Cellular and Molecular Biology India	2	1	T Targeted variant analysis
F2 Single Gene Fulgent Genetics United States	4	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Coagulation Deficiency NGS Panel Fulgent Genetics United States	56	24	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Clinical Exome Fulgent Genetics United States	5129	4672	D Deletion/duplication analysis C Sequence analysis of the entire coding region

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Results: 21 to 40 of 44

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 44

Results: 21 to 40 of 44