Filters

See more specimen types...
See more states

Other countries

Results: 1 to 20 of 43 (representing 22 labs)

Tests names and labsConditionsGenes and analytesMethods

qCarrier Plus

Quantitative Genomic Medicine Laboratories, SL
Spain
328300
  • C Sequence analysis of the entire coding region

Ehlers-Danlos Syndrome Sequencing Panel

PreventionGenetics
United States
1818
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

ADAMTS2. Complete sequencing

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

Ehlers-Danlos Syndrome Type VIIC , Sequencing ADAMTS2 Gene

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

GeneAware Ashkenazi Jewish Panel Version 2 (Male)

Baylor Miraca Genetics Laboratories
United States
4437
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

GeneAware Ashkenazi Jewish Panel Version 2 (Female)

Baylor Miraca Genetics Laboratories
United States
4739
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

GeneAware Complete Panel Version 2 (Male)

Baylor Miraca Genetics Laboratories
United States
164149
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

GeneAware Complete Panel Version 2 (Female)

Baylor Miraca Genetics Laboratories
United States
175159
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Invitae Ehlers-Danlos Syndrome Panel

Invitae
United States
3514
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Connective Tissue Focus Panel

Courtagen Diagnostics Laboratory Courtagen Life Sciences
United States
14783
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Ehlers-Danlos Syndrome Spotlight Panel

Courtagen Diagnostics Laboratory Courtagen Life Sciences
United States
1710
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Inheritest NGS, Comprehensive

Integrated Genetics Westborough Integrated Genetics
United States
136141
  • T Targeted variant analysis

EHLERS-DANLOS, SYNDROME

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
1111
  • C Sequence analysis of the entire coding region

Inheritest NGS, Ashkenazi Jewish Ancestry Panel

Integrated Genetics Westborough Integrated Genetics
United States
4039
  • T Targeted variant analysis

Ehlers-Danlos syndrome type VIIC

Integrated Genetics Westborough Integrated Genetics
United States
11
  • C Sequence analysis of the entire coding region

NGS panel - Ehlers-Danlos syndromes (Ehlers-Danlos type IV - vascular type - excluded)

Genome Diagnostics VU University Medical Center
Netherlands
1520
  • D Deletion/duplication analysis
  • S Mutation scanning of the entire coding region
  • T Targeted variant analysis

NGS panel - Ehlers-Danlos syndromes (Ehlers-Danlos type IV - vascular type - excluded) + FLNA

Genome Diagnostics VU University Medical Center
Netherlands
1421
  • D Deletion/duplication analysis
  • T Targeted variant analysis

NGS panel - Ehlers-Danlos syndromes (Ehlers-Danlos type IV - vascular type - excluded) + COL3A1

Genome Diagnostics VU University Medical Center
Netherlands
1421
  • D Deletion/duplication analysis
  • T Targeted variant analysis

NGS panel - Ehlers-Danlos syndromes (Ehlers-Danlos type IV - vascular type - excluded)

Genome Diagnostics VU University Medical Center
Netherlands
1420
  • D Deletion/duplication analysis
  • T Targeted variant analysis

NGS panel - Ehlers-Danlos syndromes (Ehlers-Danlos type IV - vascular type - excluded) + FN1

Genome Diagnostics VU University Medical Center
Netherlands
1321
  • D Deletion/duplication analysis
  • T Targeted variant analysis

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.

Support Center