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Results: 1 to 20 of 31

Tests names and labsConditionsGenes, analytes, and microbesMethods

Carpal tunnel syndrome, familial, 115430, Autosomal dominant; CTS1 (TTR gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

NeuromuscularZoom

Johns Hopkins Genomics DNA Diagnostic Laboratory Johns Hopkins Hospital
United States
480254
  • C Sequence analysis of the entire coding region

RenalZoom

Johns Hopkins Genomics DNA Diagnostic Laboratory Johns Hopkins Hospital
United States
527338
  • C Sequence analysis of the entire coding region

TTR gene sequence and deletion/duplication

Ambry Genetics
United States
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

HCMFirst® reflex HCMNext®

Ambry Genetics
United States
5830
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

HCMNext®

Ambry Genetics
United States
5830
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

DCMNext®

Ambry Genetics
United States
10037
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CustomNext-Cardio®

Ambry Genetics
United States
236167
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CMNext®

Ambry Genetics
United States
13856
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CardioNext®

Ambry Genetics
United States
18992
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Arrhythmia & Cardiomyopathy Panel, Comprehensive

CNH Molecular Diagnostics Laboratory Childrens National Hospital
United States
21193
  • C Sequence analysis of the entire coding region

Cardiomyopathy Panel, Comprehensive

CNH Molecular Diagnostics Laboratory Childrens National Hospital
United States
17071
  • C Sequence analysis of the entire coding region

Cardiomyopathy Panel, Hypertrophic

CNH Molecular Diagnostics Laboratory Childrens National Hospital
United States
8535
  • C Sequence analysis of the entire coding region

Cardiomyopathy Panel, Dilated

CNH Molecular Diagnostics Laboratory Childrens National Hospital
United States
13448
  • C Sequence analysis of the entire coding region

Transthyretin Amyloidosis (TTR Single Gene Test)

Fulgent Genetics
United States
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Cardiomyopathy NGS Panel

Fulgent Genetics
United States
450128
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Paroxysmal Extreme Pain Disorder NGS Panel

Fulgent Genetics
United States
18553
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Single gene testing TTR

CeGaT GmbH
Germany
21
  • C Sequence analysis of the entire coding region

TTR

Institute of Human Genetics Medical University Innsbruck
Austria
31
  • S Mutation scanning of the entire coding region

TTR Single Gene

Fulgent Genetics
United States
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 31

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.