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Results: 1 to 16 of 16

Tests names and labsConditionsGenes, analytes, and microbesMethods

EWSR1 - NGS including CNV analysis

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

CentoNeuro Panel

Centogene AG - the Rare Disease Company
Germany
18861858
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Amyotrophic Lateral Sclerosis (ALS) / Dementia Panel

Centogene AG - the Rare Disease Company
Germany
6466
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Endeavor

PathGroup
United States
73505
  • C Sequence analysis of the entire coding region

Ewing sarcoma, 612219; ES (Ewing sarcoma) (EWSR1 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

Neuroepithelioma, 612219 (Neuroepithelioma) (EWSR1 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

Solid and brain tumor fusion panel

Laboratory for Molecular Pediatric Pathology Boston Children's Hospital
United States
1426
  • E Sequence analysis of select exons

Detection by FISH of EWSR1 rearrangements (sarcoma Ewing)

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

EWS-FLI1 t(11;22) (PNET) RT-PCR

Duzen Laboratories Duzen BBAGUAS
Turkey
21
  • R RNA analysis

EWSR1 rearrangements

Duzen Laboratories Duzen BBAGUAS
Turkey
31
  • I FISH-interphase

Ewing Sarcoma NGS Fusion Panel

NeoGenomics Laboratories NeoGenomics Laboratories, Inc.
United States
12
  • C Sequence analysis of the entire coding region

FISH - Solid Tumor

Warren G. Sanger Human Genetics Laboratory Nebraska Medicine (formerly a UNMC Lab)
United States
2241
  • F Fluorescence in situ hybridization (FISH)

EWSR1 Single Gene

Fulgent Genetics
United States
171
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Ewing sarcoma IFISH

Cytogenetics Laboratory University of Washington
United States
11
  • I FISH-interphase

Hemato-oncology chromosomal microarray

Pittsburgh Cytogenetics Laboratory University of Pittsburgh Medical Center
United States
2393
  • D Deletion/duplication analysis
  • H Detection of homozygosity

Clinical Exome

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

Results: 1 to 16 of 16

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.