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Results: 61 to 73 of 73

Tests names and labsConditionsGenes, analytes, and microbesMethods

Hereditary Breast/Gyn Cancer Panel

Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia
United States
2828
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Renal/Urinary Tract Cancers Panel

Invitae
United States
3724
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Multi-Cancer Panel

Invitae
United States
13980
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Small Cell Carcinoma of the Ovary Hypercalcemic Type Test

Invitae
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Rhabdoid Tumor Predisposition Syndrome Panel

Invitae
United States
42
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Common Hereditary Cancers Panel (Breast, Gyn, GI)

Invitae
United States
7542
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

SMARCA4

MGZ Medical Genetics Center
Germany
21
  • C Sequence analysis of the entire coding region

SMARCA4 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

SMARCA4 Single Gene

Fulgent Genetics
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51274672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Intellectual Disability NGS Panel

Fulgent Genetics
United States
1057554
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Rhabdoid tumor predisposition syndrome 2

MedGene
Slovakia
11
  • C Sequence analysis of the entire coding region

Rhabdoid tumor predisposition syndrome 2

Praxis fuer Humangenetik Wien
Austria
11
  • C Sequence analysis of the entire coding region

Results: 61 to 73 of 73

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.