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Results: 1 to 20 of 75

Tests names and labsConditionsGenes, analytes, and microbesMethods

Hereditary Cancer Screening - Nervous System & Endocrine Cancer Panel (44 Genes)

Genesys Diagnostics Genesys Diagnostics, Inc.
United States
5244
  • X Mutation scanning of select exons

Hereditary Cancer Screening - Full Hereditary Cancer Panel (99 Genes)

Genesys Diagnostics Genesys Diagnostics, Inc.
United States
10999
  • X Mutation scanning of select exons

AIP Gene Pituitary adenoma, ACTH-secreting, due to AIP germline mutation NGS Genetic DNA Test

DNA Labs India
India
11
  • S Mutation scanning of the entire coding region

AIP Gene Pituitary adenoma, growth hormone-secreting, due to AIP germline mutation NGS Genetic DNA Test

DNA Labs India
India
11
  • S Mutation scanning of the entire coding region

AIP Gene Pituitary adenoma, prolactin-secreting, due to AIP germline mutation NGS Genetic DNA Test

DNA Labs India
India
11
  • S Mutation scanning of the entire coding region

Hereditary Endocrine Cancer Panel

Mayo Clinic Laboratories Mayo Clinic
United States
124
  • C Sequence analysis of the entire coding region

Hereditary Expanded Cancer Panel

Mayo Clinic Laboratories Mayo Clinic
United States
186
  • C Sequence analysis of the entire coding region

Familial isolated pituitary adenoma

Molecular Genetics Laboratory North York General Hospital
Canada
11
  • C Sequence analysis of the entire coding region

Comprehensive cancer panel (76 genes)

Molecular Genetics Laboratory North York General Hospital
Canada
174
  • T Targeted variant analysis

AIP - NGS including CNV analysis

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Diabetes and Obesity Panel

Centogene AG - the Rare Disease Company
Germany
247262
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Invitae Multi-Cancer + RNA Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
14263
  • D Deletion/duplication analysis

Penn Cancer Grant Panel

Ambry Genetics
United States
7980
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Pituitary adenoma, ACTH-secreting, 219090, Autosomal recessive (Cushing disease) (MLPA)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • D Deletion/duplication analysis

Pituitary adenoma, prolactin-secreting, 600634 (Familial isolated pituitary adenoma) (MLPA)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • D Deletion/duplication analysis

Pituitary adenoma, growth hormone-secreting, 102200, Autosomal dominant, Somatic mutation (Acromegaly) (AIP gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Pituitary adenoma, ACTH-secreting, 219090, Autosomal recessive (Cushing disease) (AIP gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Pituitary adenoma, prolactin-secreting, 600634 (Familial isolated pituitary adenoma) (AIP gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Invitae Familial Isolated Pituitary Adenomas Test

Labcorp Genetics (formerly Invitae) LabCorp
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Genetic Health Screen

Labcorp Genetics (formerly Invitae) LabCorp
United States
409164
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 75

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.