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Results: 1 to 20 of 111 (representing 70 labs)

Tests names and labsConditionsGenes and analytesMethods

CentoICU platinum

Centogene AG - the Rare Disease Company
Germany
769514
  • C Sequence analysis of the entire coding region

CentoICU platinum plus

Centogene AG - the Rare Disease Company
Germany
769514
  • C Sequence analysis of the entire coding region

Prothrombin-Related Thrombophilia

Clinical Molecular Genetics Laboratory Johns Hopkins All Children's Hospital
United States
11
  • E Sequence analysis of select exons
  • T Targeted variant analysis

Prothrombin-Related Thrombophilia

Genetics Laboratory Shodair Children's Hospital
United States
10
  • T Targeted variant analysis

MTHFR

Genelex
United States
41
  • T Targeted variant analysis

Factor II deficiency

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Prothrombin (Factor II) Gene mutation

Molecular Diagnostics Children's Hospital of Wisconsin
United States
11
  • T Targeted variant analysis

Factor V Leiden

IBC Instituto de Bioquimica Clinica SRL
Argentina
21
  • X Mutation scanning of select exons

Factor II

Castle Medical Molecular Diagnostics Castle Medical, LLC
United States
21
  • T Targeted variant analysis

MTHFR, FII, FV. Simultaneous analysis of the polymorphims FII (20210G>A), FV (p.Arg506Gln) and MTHFR (c.677C>T)

Instituto de Medicina Genomica
Spain
23
  • T Targeted variant analysis

MTHFR, FII, FV. Simultaneous analysis of the polymorphims FII (20210G>A), FV (p.Arg506Gln), MTHFR (c.677C>T) and MTHFR (c.1298A>C)

Instituto de Medicina Genomica
Spain
23
  • T Targeted variant analysis

MTHFR, FII, FV, PAI. Simultaneous analysis of the polymorphims FII (c.20210G>A), FV (p.R506Q), MTHFR (c.677C>T) and 5G/4G in the 5´UTR region of the PAI gene

Instituto de Medicina Genomica
Spain
34
  • T Targeted variant analysis

F2. Complete sequencing

Instituto de Medicina Genomica
Spain
41
  • C Sequence analysis of the entire coding region

Prothrombin Mutation Analysis

Molecular Pathology Laboratory University of Pennsylvania Health System
United States
11
  • T Targeted variant analysis

Thrombophilia Mutation Panel

Baylor Miraca Genetics Laboratories Baylor College of Medicine
United States
113
  • T Targeted variant analysis

Prothrombin Mutation Panel

Baylor Miraca Genetics Laboratories Baylor College of Medicine
United States
41
  • T Targeted variant analysis

MTHFR Thermolabile Variant Analysis

Baylor Miraca Genetics Laboratories Baylor College of Medicine
United States
41
  • T Targeted variant analysis

Thrombotic Risk, Inherited Etiologies (Most Common) with Reflex to Factor V Leiden

ARUP Laboratories, Molecular Genetics and Genomics
United States
16
  • A Analyte
  • T Targeted variant analysis

MitoMet®Plus aCGH Analysis

Baylor Miraca Genetics Laboratories Baylor College of Medicine
United States
845637
  • D Deletion/duplication analysis

Prothrombin

Center for Genetics at Saint Francis Saint Francis Hospital
United States
11
  • T Targeted variant analysis

Results: 1 to 20 of 111

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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