Filters

See more specimen types...

Other countries

Results: 1 to 20 of 29

Tests names and labsConditionsGenes and analytesMethods

CentoICU platinum

Centogene AG - the Rare Disease Company
Germany
768514
  • C Sequence analysis of the entire coding region

CentoICU platinum plus

Centogene AG - the Rare Disease Company
Germany
768514
  • C Sequence analysis of the entire coding region

Feingold syndrome

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

Facial Dysostosis Sequencing Panel

Genetic Services Laboratory University of Chicago
United States
1417
  • C Sequence analysis of the entire coding region

Skeletal Disorders and Joint Problems Sequencing Panel

PreventionGenetics
United States
327258
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

MYCN. Complete sequencing

Instituto de Medicina Genomica
Spain
11
  • C Sequence analysis of the entire coding region

Alveolar capillary dysplasia with misalignment of pulmonary veins (deletions/duplications analysis of 16q24.1 region)

CGC Genetics
Portugal
33
  • D Deletion/duplication analysis

Alveolar capillary dysplasia with misalignment of pulmonary veins (deletions/duplications analysis of 16q24.1 region)

CGC Genetics
Portugal
33
  • D Deletion/duplication analysis

FEINGOLD SYNDROME TYPE 1

Laboratorio de Genetica Clinica SL
Spain
11
  • C Sequence analysis of the entire coding region

Feingold Syndrome, Sequencing MYCN Gene

Reference Laboratory Genetics
Spain
11
  • C Sequence analysis of the entire coding region

Craniofacial Seq Analysis

Division of Genomic Diagnostics The Children's Hospital of Philadelphia
United States
4043
  • C Sequence analysis of the entire coding region

Craniofacial Seq + Del/Dup Panel

Division of Genomic Diagnostics The Children's Hospital of Philadelphia
United States
4043
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Craniofacial Del/Dup Panel

Division of Genomic Diagnostics The Children's Hospital of Philadelphia
United States
4043
  • D Deletion/duplication analysis

Feingold syndrome: deletions-duplications analysis (MLPA) MYCN gene

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
11
  • D Deletion/duplication analysis

Detection by FISH of MYCN

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

Single gene testing MYCN

CeGaT GmbH
Germany
11
  • C Sequence analysis of the entire coding region

qChip

Quantitative Genomic Medicine Laboratories, SL
Spain
184162
  • D Deletion/duplication analysis

MYCN Gene Sequencing

GeneDx
United States
11
  • S Mutation scanning of the entire coding region

MYCN

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

Skeletal Dysplasias NGS panel

Fulgent Genetics
United States
370161
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 29

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.

Support Center