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Results: 1 to 20 of 29

Tests names and labsConditionsGenes, analytes, and microbesMethods

Cystic Kidney Disease Gene Panel

Mayo Clinic Laboratories Mayo Clinic
United States
1644
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Tuberous Sclerosis Gene Panel

Mayo Clinic Laboratories Mayo Clinic
United States
32
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

TUBEROUS SCLEROSIS

Clinical Genomics Unit Hospital Universitari Germans Trias i Pujol
Spain
32
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

myRisk Hereditary Cancer

Myriad Genetics, Inc.
United States
3248
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hereditary Cystic and Glomerular Disorders Panel

Genetic Services Laboratory University of Chicago
United States
1764
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Hereditary Cancer Panel (66 Genes)

Quest Diagnostics Nichols Institute San Juan Capistrano
United States
3566
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Tuberous Sclerosis Complex Panel (TSC1 and TSC2)

Quest Diagnostics Nichols Institute San Juan Capistrano
United States
32
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Tuberous Sclerosis Complex Panel, Sequencing and Deletion/Duplication, Fetal

ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories
United States
32
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Tuberous Sclerosis Complex Panel, Sequencing and Deletion/Duplication

ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories
United States
32
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Prenatal Tuberous Sclerosis Panel

GeneDx
United States
12
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Tuberous Sclerosis Panel

GeneDx
United States
12
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Tuberous Sclerosis Panel

Blueprint Genetics
Finland
12
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Hereditary Cancer Panel

Blueprint Genetics
Finland
14146
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Cystic Lung Disease Panel

Blueprint Genetics
Finland
58
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Pulmonology Panel

Blueprint Genetics
Finland
566
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Pediatric Solid Tumors Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
9048
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

NTHL1 Single Gene

Fulgent Genetics
United States
41
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Colorectal Cancer Comprehensive Panel

Fulgent Genetics
United States
7722
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Full Comprehensive Cancer Panel

Fulgent Genetics
United States
329127
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hereditary Tubulopathy and Nephrolithiasis Panel

Genetic Services Laboratory University of Chicago
United States
1275
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 29

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.