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Results: 1 to 20 of 27 (representing 21 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

Antithrombin III deficiency

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

Antithrombin Deficiency via the SERPINC1 Gene

PreventionGenetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Hereditary Thrombophilia (Antithrombin III. Cambridge I/II Deficiency), Sequencing SERPINC1 Gene

Reference Laboratory Genetics
Spain
11
  • C Sequence analysis of the entire coding region

ANTITHROMBIN III DEFICIENCY

Laboratorio de Genetica Clinica SL
Spain
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Antithrombin III deficiency

Labor Dr. Wisplinghoff
Germany
11
  • C Sequence analysis of the entire coding region

Antithrombin III deficiency

LifeLabs Genetics
Canada
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Single gene testing SERPINC1

CeGaT GmbH
Germany
11
  • C Sequence analysis of the entire coding region

Thrombophilia, Hereditary: SERPINC1 gene deletions-duplications analysis (MLPA)

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
11
  • D Deletion/duplication analysis

Thrombophilia, Hereditary: SERPINC1 gene sequence analysis

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
11
  • C Sequence analysis of the entire coding region

Platelets, Coagulation disorders Panel

CeGaT GmbH
Germany
1717
  • C Sequence analysis of the entire coding region

aCGH Deletion/Duplication Analysis

BloodCenter of Wisconsin Diagnostic Laboratories BloodCenter of Wisconsin
United States
6065
  • D Deletion/duplication analysis

SERPINC1

Division Human Genetics Medical University Innsbruck
Austria
11
  • S Mutation scanning of the entire coding region

Antithrombin deficiency, SERPINC1 sequencing

Molecular Diagnostics Laboratory Seoul National University Hospital
South Korea
11
  • C Sequence analysis of the entire coding region

Thrombophilia (p.Ser114Asn e p.Ala416Ser mutations on SERPINC1 gene)

CGC Genetics
Portugal
11
  • C Sequence analysis of the entire coding region

SERPINC1

Fulgent Genetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Hereditary Thrombophilia Panel

Invitae
United States
95
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Antithrombin III Deficiency Test

Invitae
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Thrombophilia, Hereditary (Antithrombin III. Cambridge I/II): SERPINC1 gene mutation analysis (A384P/S)

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
11
  • T Targeted variant analysis

Results: 1 to 20 of 27

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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