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Results: 1 to 20 of 26 (representing 10 labs)

Tests names and labsConditionsGenes and analytesMethods

Senior-Loken syndrome 7

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

Comprehensive Inherited Retinal Dystrophies (includes RPGR ORF15) Sequencing Panel

PreventionGenetics
United States
299280
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Nephronophthisis / Senior-Loken Syndrome and Bardet-Biedl Syndrome via the SDCCAG8 Gene

PreventionGenetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Ciliopathy Sequencing Panel

PreventionGenetics
United States
9293
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Nephronophthisis and Senior-Loken Syndrome Sequencing Panel

PreventionGenetics
United States
1718
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Ciliopathy Focus Panel

Courtagen Diagnostics Laboratory Courtagen Life Sciences
United States
218152
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Monogenic Obesity Spotlight Panel

Courtagen Diagnostics Laboratory Courtagen Life Sciences
United States
4933
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Senior-Loken Syndrome Spotlight Panel

Courtagen Diagnostics Laboratory Courtagen Life Sciences
United States
219
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Bardet-Biedl Syndrome Spotlight Panel

Courtagen Diagnostics Laboratory Courtagen Life Sciences
United States
2816
  • C Sequence analysis of the entire coding region

Ciliopathies

Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health and Science University
United States
44116
  • C Sequence analysis of the entire coding region

Senior-Loken syndrome 7 (sequence analysis of SDCCAG8 gene)

CGC Genetics
Portugal
11
  • C Sequence analysis of the entire coding region

Bardet-Biedl syndrome panel

Molecular Vision Laboratory
United States
3823
  • C Sequence analysis of the entire coding region

Retinal Dystrophy Panel

Molecular Vision Laboratory
United States
372287
  • C Sequence analysis of the entire coding region

Senior-Loken Syndrome Panel

CeGaT GmbH
Germany
1412
  • C Sequence analysis of the entire coding region

Senior Loken Syndrome Panel

CeGaT GmbH
Germany
1112
  • C Sequence analysis of the entire coding region

Senior Loken Syndrome Panel

CeGaT GmbH
Germany
1412
  • C Sequence analysis of the entire coding region

SDCCAG8

Fulgent Genetics
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Ciliopathies: Sequencing and Deletion/Duplication Panel

Emory Genetics Laboratory Emory University
United States
165112
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Senior-Loken Syndrome: Sequencing and Deletion/Duplication Panel

Emory Genetics Laboratory Emory University
United States
157
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Eye Disorders: Comprehensive Sequencing and Deletion/Duplication Panel

Emory Genetics Laboratory Emory University
United States
320207
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 26

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.

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