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Results: 1 to 20 of 50

Tests names and labsConditionsGenes, analytes, and microbesMethods

NGS Oncology Melanoma Profile (Tissue Only)

Diagnostic Laboratory Services, Inc.
United States
141
  • C Sequence analysis of the entire coding region

OnkoRisk Hereditary Oncology Plus Panel

BioReference Health
United States
9777
  • C Sequence analysis of the entire coding region

OnkoRisk Hereditary Oncology Management Panel

BioReference Health
United States
4717
  • C Sequence analysis of the entire coding region

OnkoRisk Women's Hereditary Cancer Panel

BioReference Health
United States
3418
  • C Sequence analysis of the entire coding region

OnkoRisk Hereditary Urology Panel

BioReference Health
United States
2719
  • C Sequence analysis of the entire coding region

NGS Oncology Tumor Profile

Diagnostic Laboratory Services, Inc.
United States
540
  • C Sequence analysis of the entire coding region

Hereditary Melanoma and/or Pancreatic Cancer, CDKN2A Gene

GeneKor MSA
Greece
31
  • C Sequence analysis of the entire coding region

Endeavor

PathGroup
United States
73505
  • C Sequence analysis of the entire coding region

UCSF500 Cancer Gene Panel

Clinical Cancer Genomics Laboratory University of California, San Francisco
United States
22
  • C Sequence analysis of the entire coding region

Melanoma Cancer Panel

IntelligeneCG LLC
United States
139
  • C Sequence analysis of the entire coding region

Hereditary Lymphoid/Immunodeficiency Predisposition Panel

Genetic Services Laboratory University of Chicago
United States
2766
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

OnkoSight Advanced Melanoma NGS

BioReference Health
United States
127
  • C Sequence analysis of the entire coding region

Familial Cutaneous Malignant Melanoma

GeneDx
United States
39
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

NeoTYPE® Melanoma Profile

NeoGenomics Laboratories NeoGenomics Laboratories, Inc.
United States
122
  • F Fluorescence in situ hybridization (FISH)
  • C Sequence analysis of the entire coding region

TERT Promoter Mutation Analysis

NeoGenomics Laboratories NeoGenomics Laboratories, Inc.
United States
51
  • C Sequence analysis of the entire coding region

NTRK NGS Fusion Panel

NeoGenomics Laboratories NeoGenomics Laboratories, Inc.
United States
83
  • C Sequence analysis of the entire coding region

NTRK & RET NGS Fusion Panel

NeoGenomics Laboratories NeoGenomics Laboratories, Inc.
United States
74
  • C Sequence analysis of the entire coding region

Childhood Epilepsy NGS Panel

Fulgent Genetics
United States
354209
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Neonatal Epilepsy NGS Panel

Fulgent Genetics
United States
509275
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Adolescent/Adult Epilepsy NGS Panel

Fulgent Genetics
United States
18282
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 50

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.