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Results: 21 to 40 of 106

Tests names and labsConditionsGenes, analytes, and microbesMethods

GeneSeq PLUS, Fetal Analysis

Integrated Genetics Westborough LabCorp
United States
292597
  • C Sequence analysis of the entire coding region

Partner Reflex to GeneSeq

Integrated Genetics Westborough LabCorp
United States
330746
  • C Sequence analysis of the entire coding region

Inheritest 500 PLUS Panel

Integrated Genetics Westborough LabCorp
United States
287578
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Hemochromatosis Panel

Mendelics
Brazil
16
  • C Sequence analysis of the entire coding region

HEMOCHROMATOSIS HYPERFERRITINEMIA SYNDROME PANEL

Laboratorio de Genetica Clinica SL
Spain
18
  • E Sequence analysis of select exons

SUDDEN DEATH/ IDIOPATHIC VENTRICULAR FIBRILLATION EXOME PANEL

Laboratorio de Genetica Clinica SL
Spain
1394
  • E Sequence analysis of select exons

Inherited Metabolic Disorders Panel

Dhiti Omics Technologies Private Ltd
India
376317
  • 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

Hemochromatosis Panel by Sanger Sequencing

Baylor Genetics
United States
15
  • 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

Hereditary hemochromatosis (HFE2, HAMP, TFR2, SLC40A1, FTH1)

Center for Human Genetics Cliniques Universitaires Saint Luc
Belgium
15
  • S Mutation scanning 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 NGS Panel

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

Juvenile Hereditary Hemochromatosis: gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
12
  • C Sequence analysis of the entire coding region

HEMOCHROMATOSIS TYPE 2

Laboratorio de Genetica Clinica SL
Spain
22
  • 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
14434
  • D Deletion/duplication analysis
  • 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

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

Results: 21 to 40 of 106

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.