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Results: 21 to 40 of 42

Tests names and labsConditionsGenes, analytes, and microbesMethods

Comprehensive Bleeding Disorder Panel

Versiti Diagnostic Laboratories Versiti, Inc
United States
8050
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Female Infertility

Asper Biogene Asper Biogene LLC
Estonia
8564
  • C Sequence analysis of the entire coding region

Super Panel Plus

NxGen MDx
United States
116117
  • 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
66
  • 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
2122
  • 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
2520
  • D Deletion/duplication analysis
  • S Mutation scanning of the entire coding region

Thrombosis Disorder NGS Panel

Fulgent Genetics
United States
4618
  • 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
14682
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Beacon Expanded Female Carrier Screening Plus Panel

Fulgent Genetics
United States
716335
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Beacon Expanded Male Carrier Screening Plus Panel

Fulgent Genetics
United States
661306
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Coagulation Disorders

Asper Biogene Asper Biogene LLC
Estonia
2116
  • C Sequence analysis of the entire coding region

Prothrombin polymorphism in thrombophilia

Genetics Service Unit BRIC-National Institute of Biomedical Genomics
India
11
  • T Targeted variant analysis

Single gene testing F2

CeGaT GmbH
Germany
21
  • C Sequence analysis of the entire coding region

Factor II mutation study

Diagnostics Division CENTRE FOR DNA FINGERPRINTING AND DIAGNOSTICS
India
11
  • E Sequence analysis of select exons

Thrombophilia

Centre for cellular and molecular biology Centre for Cellular and Molecular Biology
India
21
  • T Targeted variant analysis

F2 Single Gene

Fulgent Genetics
United States
41
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Coagulation Deficiency NGS Panel

Fulgent Genetics
United States
5624
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51284672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Factor 2 deficiency

MedGene
Slovakia
11
  • C Sequence analysis of the entire coding region

Factor 2 deficiency

Praxis fuer Humangenetik Wien
Austria
11
  • C Sequence analysis of the entire coding region

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.