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Results: 21 to 40 of 41

Tests names and labsConditionsGenes, analytes, and microbesMethods

SLC40A1 Sequence Analysis (Familial Mutation/Variant Analysis)

Baylor Genetics
United States
11
  • E Sequence analysis of select exons

SLC40A1 Sequence Analysis (Prenatal Diagnosis)

Baylor Genetics
United States
11
  • E Sequence analysis of select exons

Hemochromatosis: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
76
  • C Sequence analysis of the entire coding region

Comprehensive Metabolism NGS Panel

Fulgent Genetics
United States
602355
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hemochromatosis Type 4 (SLC40A1 Single Gene Test)

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

Hemochromatosis NGS Panel

Fulgent Genetics
United States
127
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hemochromatosis

Asper Biogene Asper Biogene LLC
Estonia
105
  • C Sequence analysis of the entire coding region

HEMOCHROMATOSIS TYPE 4

Laboratorio de Genetica Clinica SL
Spain
22
  • C Sequence analysis of the entire coding region

Hemochromatosis type 4

Labor Dr. Wisplinghoff
Germany
11
  • 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

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

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

SLC40A1 Single Gene

Fulgent Genetics
United States
11
  • D Deletion/duplication analysis
  • 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

Comprehensive Cardiovascular NGS Panel

Fulgent Genetics
United States
671250
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

SLC40A1-Related Hereditary Hemochromatosis (Ferroportin disease)

MVZ Dr. Eberhard & Partner Dortmund
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

SLC40A1-Related Hereditary Hemochromatosis

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

SLC40A1-Related Hereditary Hemochromatosis

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

Results: 21 to 40 of 41

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.