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Results: 1 to 20 of 30

Tests names and labsConditionsGenes, analytes, and microbesMethods

F12 Gene, Full Gene Next-Generation Sequencing

Mayo Clinic Laboratories Mayo Clinic
United States
21
  • C Sequence analysis of the entire coding region

Factor XII deficiency (F12 gene)

Molecular Genetics and Cytogenetics, Clinical Laboratory Service RED DE SALUD UC CHRISTUS
Chile
11
  • T Targeted variant analysis

F12 - NGS including CNV analysis

Centogene AG - the Rare Disease Company
Germany
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Hereditary Angioedema Panel

Invitae
United States
54
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Factor XII deficiency, 234000, Autosomal recessive (Congenital factor XII deficiency) (F12 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Factor XII deficiency, 234000, Autosomal recessive (Congenital factor XII deficiency) (MLPA)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • D Deletion/duplication analysis

Bleeding Disorders Panel

PreventionGenetics, part of Exact Sciences
United States
7879
  • 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
2120
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Clotting factor deficiency panel. 16-gene NGS panel.

Genologica Medica
Spain
2916
  • C Sequence analysis of the entire coding region

Bleeding disorder / coagulopathy panel. NGS panel of 62 genes.

Genologica Medica
Spain
9662
  • C Sequence analysis of the entire coding region

Factor XII deficiency

Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Factor XII (HAE) mutation analysis

Genetiks Genetic Diagnosis Center Genetic Diseases Evaluation Center
Turkey
11
  • C Sequence analysis of the entire coding region

Comprehensive Thrombotic Microangiopathy NGS Panel

Fulgent Genetics
United States
5837
  • 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

Focus Thrombotic Microangiopathy NGS Panel

Fulgent Genetics
United States
4022
  • 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

Bleeding Disorders , Panel Massive Sequencing (NGS) 23 Genes

Reference Laboratory Genetics
Spain
2222
  • C Sequence analysis of the entire coding region

HEREDITARY THROMBOPHILIA

Laboratorio de Genetica Clinica SL
Spain
33
  • T Targeted variant analysis

Congenital Factor XII Deficiency , Sequencing F12 Gene

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

FACTOR XII DEFICIENCY

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

Results: 1 to 20 of 30

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.