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Results: 1 to 13 of 13

Tests names and labsConditionsGenes, analytes, and microbesMethods

ACTG2 - NGS including CNV analysis

Centogene AG - the Rare Disease Company
Germany
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Visceral myopathy, 155310, Autosomal dominant; VSCM (Familial visceral myopathy) (ACTG2 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

Congenital Diarrhea and Enteropathies Panel

PreventionGenetics, part of Exact Sciences
United States
241157
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Congenital Abnormalities of the Kidney and Urinary Tract (CAKUT) Panel

PreventionGenetics, part of Exact Sciences
United States
8278
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Renal malformation panel. NGS panel of 22 genes.

Genologica Medica
Spain
4422
  • C Sequence analysis of the entire coding region

MYLK Deletion/duplication analysis

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
21
  • D Deletion/duplication analysis

Mito Genome Sequencing & Deletion Testing

GeneDx
United States
242
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

FAMILIAL VISCERAL MYOPATHY

Laboratorio de Genetica Clinica SL
Spain
11
  • C Sequence analysis of the entire coding region

ACTG2 Single Gene

Fulgent Genetics
United States
351
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

ACTG2 Sequencing

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
11
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Visceral Myopathy (ACTG2)

Center for Human Genetics, Inc
United States
11
  • C Sequence analysis of the entire coding region

Single gene testing ACTG2

CeGaT GmbH
Germany
11
  • C Sequence analysis of the entire coding region

ACTG2

MGZ Medical Genetics Center
Germany
21
  • C Sequence analysis of the entire coding region

Results: 1 to 13 of 13

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.