U.S. flag

An official website of the United States government

Filters

reset all

Other countries

Results: 1 to 20 of 43

Tests names and labsConditionsGenes, analytes, and microbesMethods

Hereditary Cancer Testing - Full Panel (76) AIP, APC, ATM, AXIN2, BAP1, BARD1, BMPR1A, BRCA1, BRCA2, BRIP1, CDC73, CDH1, CDK4, CDKN1B, CDKN2A, CHEK2, CTNN1, DICER1, EGFR, EGLN1, EPCAM, EXT1, EXT2, FH, FLCN, GALNT12, GREM1, HOXB13, KIT, LZTR1, MAX, MEN1, M

Diagnostic Medical Genetics Mount Sinai Hospital, Sinai Health System
Canada
178
  • S Mutation scanning of the entire coding region

AXIN2-related Attenuated Familial Adenomatous Polyposis

Diagnostic Medical Genetics Mount Sinai Hospital, Sinai Health System
Canada
11
  • S Mutation scanning of the entire coding region

BAP1 Tumour Predisposition Syndrome

Diagnostic Medical Genetics Mount Sinai Hospital, Sinai Health System
Canada
11
  • S Mutation scanning of the entire coding region

Birt-Hogg-Dube Syndrome

Diagnostic Medical Genetics Mount Sinai Hospital, Sinai Health System
Canada
11
  • S Mutation scanning of the entire coding region

Carney Complex

Diagnostic Medical Genetics Mount Sinai Hospital, Sinai Health System
Canada
11
  • S Mutation scanning of the entire coding region

CHRPE, CMV Thyroid, Desmoid

Diagnostic Medical Genetics Mount Sinai Hospital, Sinai Health System
Canada
11
  • S Mutation scanning of the entire coding region

CHRPE, CMV Thyroid, Desmoid with MUTYH

Diagnostic Medical Genetics Mount Sinai Hospital, Sinai Health System
Canada
12
  • S Mutation scanning of the entire coding region

DICER-associated Syndrome

Diagnostic Medical Genetics Mount Sinai Hospital, Sinai Health System
Canada
11
  • S Mutation scanning of the entire coding region

Dysplastic Nevus Syndrome

Diagnostic Medical Genetics Mount Sinai Hospital, Sinai Health System
Canada
12
  • S Mutation scanning of the entire coding region

Familial Isolated Pituitary Adenoma

Diagnostic Medical Genetics Mount Sinai Hospital, Sinai Health System
Canada
11
  • S Mutation scanning of the entire coding region

Hereditary Hyperparathyroidism

Diagnostic Medical Genetics Mount Sinai Hospital, Sinai Health System
Canada
12
  • S Mutation scanning of the entire coding region

Hereditary Leiomyomatosis and Renal Cell Cancer

Diagnostic Medical Genetics Mount Sinai Hospital, Sinai Health System
Canada
11
  • S Mutation scanning of the entire coding region

Hereditary Lung Cancer

Diagnostic Medical Genetics Mount Sinai Hospital, Sinai Health System
Canada
11
  • S Mutation scanning of the entire coding region

Li-Fraumeni Syndrome

Diagnostic Medical Genetics Mount Sinai Hospital, Sinai Health System
Canada
11
  • S Mutation scanning of the entire coding region

MEN1 Syndrome

Diagnostic Medical Genetics Mount Sinai Hospital, Sinai Health System
Canada
12
  • S Mutation scanning of the entire coding region

Multiple Endocrine Neoplasia Type 2

Diagnostic Medical Genetics Mount Sinai Hospital, Sinai Health System
Canada
11
  • S Mutation scanning of the entire coding region

Neurofibromatosis, type 1

Diagnostic Medical Genetics Mount Sinai Hospital, Sinai Health System
Canada
11
  • S Mutation scanning of the entire coding region

Nevoid Basal Cell Carcinoma Syndrome/ Gorlin Syndrome

Diagnostic Medical Genetics Mount Sinai Hospital, Sinai Health System
Canada
12
  • S Mutation scanning of the entire coding region

Nijmegen Breakage Syndrome

Diagnostic Medical Genetics Mount Sinai Hospital, Sinai Health System
Canada
11
  • S Mutation scanning of the entire coding region

Peutz-Jeghers Syndrome

Diagnostic Medical Genetics Mount Sinai Hospital, Sinai Health System
Canada
11
  • S Mutation scanning of the entire coding region

Results: 1 to 20 of 43

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.