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Results: 1 to 20 of 1354

Tests names and labsConditionsGenes, analytes, and microbesMethods

Vitamin K-dependent clotting factors, combined deficiency of, 1, 277450, Autosomal recessive; VKCFD1 (Hereditary combined deficiency of vitamin K-dependent clotting factors) (GGCX 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

Vitamin K-dependent clotting factors, combined deficiency of, 2, 607473; VKCFD2 (Hereditary combined deficiency of vitamin K-dependent clotting factors) (VKORC1 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

K/k Genotyping

Versiti Diagnostic Laboratories Versiti, Inc
United States
11
  • C Sequence analysis of the entire coding region

Kell K/k (KEL) Antigen Genotyping, Fetal

ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories
United States
11
  • T Targeted variant analysis

Kell K/k (KEL) Antigen Genotyping

ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories
United States
11
  • T Targeted variant analysis

GGCX Gene Vitamin K-dependent clotting factors combined deficiency type 1 NGS Genetic DNA Test

DNA Labs India
India
11
  • S Mutation scanning of the entire coding region

Vitamin K-dependent clotting factors, combined deficiency of: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
22
  • C Sequence analysis of the entire coding region

Vitamin k-dependent clotting factors, combined deficiency of, 1

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

Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency, 610842 (Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency) (GGCX 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

Vitamin k-dependent clotting factors, combined deficiency of, 2

Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders
Germany
11
  • 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

Hereditary combined deficiency of vitamin K-dependent clotting factors, type 2 (sequence analysis of VKORC1 gene)

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

Vitamin K-dependent clotting factors, combined deficiency of, 1 , Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency (sequence analysis of GGCX gene)

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

Detection of somatic mutations of exon 10 of MPL gene (including W515L / K)

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

Genomic Unity® Custom Analysis

Variantyx, Inc.
United States
14054
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

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

Comprehensive Bleeding Disorder Panel

Versiti Diagnostic Laboratories Versiti, Inc
United States
8050
  • 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

Coagulation Disorders

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

Results: 1 to 20 of 1354

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.