U.S. flag

An official website of the United States government

Filters

reset all
See more specimen types...

Other countries

Results: 1 to 13 of 13

Tests names and labsConditionsGenes, analytes, and microbesMethods

Solid Tumor Panel

Centogene AG - the Rare Disease Company
Germany
218135
  • C Sequence analysis of the entire coding region

Burkitt lymphoma, 113970, Isolated cases; BL (Burkitt lymphoma) (MYC 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

Detection by FISH of C-MYC (8q24) rearrangements

CGC Genetics Unilabs
Portugal
11
  • F Fluorescence in situ hybridization (FISH)

Detection by FISH of t(8;14) MYC/IGH

CGC Genetics Unilabs
Portugal
11
  • F Fluorescence in situ hybridization (FISH)

MYC (8Q24) Rearrangement

Duzen Laboratories Duzen BBAGUAS
Turkey
11
  • I FISH-interphase

Oncology FISH Analysis - MYC translocation

Baylor Genetics
United States
11
  • T Targeted variant analysis

FISH, Lymphoma Panel

Cytogenetics and Molecular Pathology Laboratory UP Health System Marquette
United States
76
  • F Fluorescence in situ hybridization (FISH)
  • K Karyotyping

t(8;14) MYC/IGH

KSL Diagnostics KSL Biomedical
United States
21
  • I FISH-interphase

8q24 cMYC

KSL Diagnostics KSL Biomedical
United States
31
  • I FISH-interphase

Chromosome Analysis: Cancer

Genomic Research Center Shahid Beheshti University of Medical Sciences
Iran
111
  • K Karyotyping

MYC Single Gene

Fulgent Genetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51294672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Chromosome Analysis: Cancer

Warren G. Sanger Human Genetics Laboratory Nebraska Medicine (formerly a UNMC Lab)
United States
251
  • K Karyotyping

Results: 1 to 13 of 13

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.