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Results: 21 to 40 of 121

Tests names and labsConditionsGenes and analytesMethods

Invitae Pediatric Solid Tumors Panel

Invitae
United States
9148
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Familial Gastrointestinal Stromal Tumor Syndrome Panel

Invitae
United States
37
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Hereditary Breast-Ovarian Cancer Panel

NeoGenomics Laboratories
United States
173
  • C Sequence analysis of the entire coding region

Comprehensive Hereditary Cancer Panel

Genetic Services Laboratory University of Chicago
United States
1750
  • C Sequence analysis of the entire coding region

Renal / Urinary Cancer Comprehensive Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
77327
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Paraganglioma-Pheochromocytoma Comprehensive Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
37111
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Sarcoma Comprehensive Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
92126
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Cancer Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
1736124
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Renal / Urinary Cancer Comprehensive Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
77327
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Mitochondrial respiratory chain complex II, III, and IV deficiency

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
1921
  • C Sequence analysis of the entire coding region

PARAGANGLIOMA-PHEOCHROMOCYTOMA

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
1011
  • C Sequence analysis of the entire coding region

ONCOLOGY, PANEL

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
6780
  • C Sequence analysis of the entire coding region

CancerNext-Expanded

Ambry Genetics
United States
3349
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hereditary Kidney Cancer Panel

Division of Genomic Diagnostics The Children's Hospital of Philadelphia
United States
2020
  • S Mutation scanning of the entire coding region

CHOP Comprehensive Hereditary Cancer Panel

Division of Genomic Diagnostics The Children's Hospital of Philadelphia
United States
92128
  • C Sequence analysis of the entire coding region

CHOP Solid Tumors Panel

Division of Genomic Diagnostics The Children's Hospital of Philadelphia
United States
1237
  • S Mutation scanning of the entire coding region

Hereditary Endocrine Cancer Panel

Division of Genomic Diagnostics The Children's Hospital of Philadelphia
United States
1215
  • S Mutation scanning of the entire coding region

Hereditary Paraganglioma/Pheochromocytoma Panel

Division of Genomic Diagnostics The Children's Hospital of Philadelphia
United States
912
  • S Mutation scanning of the entire coding region

Renal Cancer Panel

GeneDx
United States
618
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

PGL/PCC (Paraganglioma/Pheochromocytoma) Panel

GeneDx
United States
212
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 21 to 40 of 121

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.