GTR Home > Tests > Search results - Usher syndrome, type 1D

Apply filters

Showing test for 1 condition

reset

Compare labs

Your search term can be found in tests with a total of 2019 conditions. Only 1000 conditions are displayed in this filter box. Please type the name of the condition in the search box in this filter to find the specific condition. You can use the filters below to narrow down your results.
If the name of the condition you typed is not present, please try another query or search using the All GTR tab.

  • Hide states

GTR test search results for C1832845[DISCUI]

C Clinical test, R Research test

Showing 1 to 20 of 44 tests for 1 condition in 18 labs

CUsher syndrome type 1D/F

Lab: Centogene AG - the Rare Disease Company University of Rostock Rostock, Mecklenburg-Vorpommern, Germany
Test targets
Methods
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CUsher syndrome type 1D/F

Lab: Centogene AG - the Rare Disease Company University of Rostock Rostock, Mecklenburg-Vorpommern, Germany
Test targets
Methods
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CUsher Syndrome Sequencing Panel

Lab: PreventionGenetics Marshfield, Wisconsin, United States
Test targets
Methods
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis
Total conditions (10)
Total targets (11)

CTruGenome Predisposition Screen (Whole Genome Sequencing)

Lab: Illumina Clinical Services Laboratory Illumina San Diego, California, United States
Test targets
Methods
  • C Sequence analysis of the entire coding region
Total conditions (1541)
Total targets (1578)

CCDH23. Complete sequencing

Lab: Instituto de Medicina Genomica Paterna, Comunidad Valenciana, Spain
Test targets
Methods
  • C Sequence analysis of the entire coding region

CCDH23 Sequence Analysis

Lab: Baylor Miraca Genetics Laboratories Houston, Texas, United States
Test targets
Methods
  • C Sequence analysis of the entire coding region

CPCDH15 Comprehensive - Sequence & Deletion/Duplication Analysis

Lab: Baylor Miraca Genetics Laboratories Houston, Texas, United States
Test targets
Methods
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CUsher Syndrome Panel

Test targets
Methods
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
Total conditions (15)
Total targets (9)

COtoGenome Test for Hearing Loss (87 Genes)

Methods
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis
Total conditions (112)
Total targets (86)

CUsher Syndrome Type 1 and Deafness, Autosomal Recessive 23 (DFNB23) via the PCDH15 Gene

Lab: PreventionGenetics Marshfield, Wisconsin, United States
Test targets
Methods
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

CUsher Syndrome Type 1 and Deafness, Autosomal Recessive 12 (DFNB12) via the CDH23 Gene

Lab: PreventionGenetics Marshfield, Wisconsin, United States
Test targets
Methods
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

COtoSCOPE

Methods
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
Total conditions (98)
Total targets (92)

CCDH23

Lab: Fulgent Clinical Diagnostics Lab Fulgent Diagnostics Temple City, California, United States
Test targets
Methods
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
Total conditions (23)

CPCDH15

Lab: Fulgent Clinical Diagnostics Lab Fulgent Diagnostics Temple City, California, United States
Test targets
Methods
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
Total conditions (24)

CNGS Hearing Loss Panel

Methods
  • C Sequence analysis of the entire coding region
Total conditions (100)
Total targets (84)

CUSHER SYNDROME and NON-SYNDROMIC DEAFNESS

Test targets
Methods
  • C Sequence analysis of the entire coding region
Total conditions (25)
Total targets (18)

CDEAFNESS A.R. (39 genes)

Test targets
Methods
  • C Sequence analysis of the entire coding region
Total conditions (51)
Total targets (39)

CDEAFNESS A.D. and A.R.

Test targets
Methods
  • C Sequence analysis of the entire coding region
Total conditions (65)
Total targets (57)

CUsher syndrome, type 1D

Lab: Bioarray Elche, Comunidad Valenciana, Spain
Test targets
Methods
  • C Sequence analysis of the entire coding region

CUsher syndrome (NGS panel for 12 genes)

Lab: CGC Genetics Porto, Porto, Portugal
Test targets
Methods
  • C Sequence analysis of the entire coding region
Total conditions (15)
Total targets (12)

Showing 1 to 20 of 44 tests for 1 condition in 18 labs

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.