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Results: 1 to 20 of 20

Tests names and labsConditionsGenes, analytes, and microbesMethods

KRT2 Gene Ichthyosis, bullous type NGS Genetic DNA Test

DNA Labs India
India
11
  • S Mutation scanning of the entire coding region

TLL1 Gene Atrial septal defect type 6 NGS Genetic DNA Test

DNA Labs India
India
11
  • S Mutation scanning of the entire coding region

TLL1 - NGS including CNV analysis

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

CentoCardio Panel

Centogene AG - the Rare Disease Company
Germany
289275
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Nonsyndromic Congenital Heart Disease Panel

PreventionGenetics, part of Exact Sciences
United States
5444
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Atrial septal defect 6, 613087, Autosomal dominant; ASD6 (Interatrial communication) (TLL1 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

TLL1

Institute for Human Genetics University Medical Center Freiburg
Germany
11
  • C Sequence analysis of the entire coding region

Congenital Heart Defects Panel 

CGC Genetics Unilabs
Portugal
1208
  • C Sequence analysis of the entire coding region

SUDDEN DEATH/ IDIOPATHIC VENTRICULAR FIBRILLATION EXOME PANEL

Laboratorio de Genetica Clinica SL
Spain
1394
  • E Sequence analysis of select exons

HEREDITARY ARRHYTHMIA EXOME PANEL

Laboratorio de Genetica Clinica SL
Spain
1160
  • E Sequence analysis of select exons

Congenital structural heart disease panel. NGS panel of 62 genes.

Genologica Medica
Spain
11362
  • C Sequence analysis of the entire coding region

Genomic Unity® Custom Analysis

Variantyx, Inc.
United States
14054
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

Atrial septal defect: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
88
  • C Sequence analysis of the entire coding region

Structural Heart Disease NGS Panel

Fulgent Genetics
United States
7328
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Congenital Heart Defect NGS Panel

Fulgent Genetics
United States
377114
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Congenital Structural Heart Disease Panel

Blueprint Genetics
Finland
962
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Heart Diseases - panels

MGZ Medical Genetics Center
Germany
4157
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Congenital Heart Defects Panel

CeGaT GmbH
Germany
4244
  • C Sequence analysis of the entire coding region

TLL1 Single Gene

Fulgent Genetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51284672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 20

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.