GTR Home > Tests > Search results - CHRNE[gene]

Apply filters

Showing tests for all 2085 conditions

Compare labs

Your search term can be found in tests with a total of 2085 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 1145[geneid]

C Clinical test, R Research test

Showing 1 to 20 of 41 tests for 2085 conditions in 18 labs

CAllNeuro panel

Lab: Centogene AG - the Rare Disease Company Rostock, Mecklenburg-Vorpommern, Germany
Test targets
Methods
  • C Sequence analysis of the entire coding region
Total conditions (602)
Total targets (1038)

CCongenital Myasthenic Syndrome Sequencing Panel

Lab: Genetic Services Laboratory University of Chicago Chicago, Illinois, United States
Total conditions (11)
Total targets (17)

CMyasthenic syndrome, congenital

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

CCHRNA1, CHAT, CHRNE, RAPSN, DOK7, COLQ. NextGeneDx.Complete sequencing by NGS

Lab: Instituto de Medicina Genomica Paterna, Comunidad Valenciana, Spain
Test targets
Methods
  • C Sequence analysis of the entire coding region
Total targets (6)

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)

CCHRNE. Complete sequencing

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

CFetal Akinesia Deformation Sequence/Lethal Multiple Pterygium 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 (7)
Total targets (11)

CCongenital Myasthenic 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 (14)

CCongenital Myasthenic Syndrome via the CHRNE 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

CCarrierMap

Lab: Recombine New York, New York, United States
Total conditions (299)
Total targets (297)

CCongenital myasthenic syndrome

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

CMyasthenic syndrome fast channel congenital (NGS panel for 8 genes)

Lab: CGC Genetics Porto, Porto, Portugal
Test targets
Methods
  • C Sequence analysis of the entire coding region
Total targets (8)

CCongenital Myasthenic Syndromes and Arthrogryposis Panel

Lab: CeGaT GmbH Tuebingen, Baden-Wurttemberg, Germany
Total conditions (9)
Total targets (44)

CMuscle Weakness (Myopathy, Muscular Dystrophy)

Test targets
Methods
  • C Sequence analysis of the entire coding region
Total conditions (6)
Total targets (179)

Showing 1 to 20 of 41 tests for 2085 conditions 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.