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Results: 1 to 20 of 30 (representing 24 labs)

Tests names and labsConditionsGenes and analytesMethods

Hemochromatosis type 4

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

NGS Panel for Hemochromatosis and Hyperferritinemia /Hypoferritinemia Panel

BLOODGENETICS
Spain
108
  • C Sequence analysis of the entire coding region

Hyperferritinemia Panel

Molecular Genetics Laboratory London Health Sciences Centre
Canada
1515
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Hereditary Hemochromatosis via the SLC40A1 Gene

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

Hereditary Hemochromatosis Sequencing Panel

PreventionGenetics
United States
77
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

SLC40A1. Complete sequencing

Instituto de Medicina Genomica
Spain
11
  • C Sequence analysis of the entire coding region

Hemochromatosis type 4

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

Hemochromatosis type 4

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

Hereditary Hemochromatosis Spotlight Panel

Courtagen Diagnostics Laboratory Courtagen Life Sciences
United States
75
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Abnormal Glucose/MODY Spotlight Panel

Courtagen Diagnostics Laboratory Courtagen Life Sciences
United States
4931
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Abdominal Pain Spotlight Panel

Courtagen Diagnostics Laboratory Courtagen Life Sciences
United States
6944
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hereditary Hemochromatosis Panel

Blueprint Genetics
Finland
75
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Metabolism Panel

Blueprint Genetics
Finland
14354
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

SLC40A1 Gene Sequencing

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
11
  • C Sequence analysis of the entire coding region

Hemochromatosis NGS Panel

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
157
  • C Sequence analysis of the entire coding region

Hemochromatosis type 4

Bioarray
Spain
11
  • C Sequence analysis of the entire coding region

Single gene testing SLC40A1

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

Genetic disorders with abnormal pigmentation Panel

CeGaT GmbH
Germany
2932
  • C Sequence analysis of the entire coding region

SLC40A1 Sequencing

Molecular Genetics Laboratory Cincinnati Children's Hospital Medical Center
United States
11
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

SLC40A1

Fulgent Genetics
United States
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.

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