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Results: 21 to 38 of 38

Tests names and labsConditionsGenes, analytes, and microbesMethods

Hereditary Cancer Panel (Complete)

Mendelics
Brazil
1264
  • 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

Vascular malformations panel. 14-gene NGS panel.

Genologica Medica
Spain
3814
  • 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

Vascular Anomalies (VANseq) Expanded Del/Dup Panel

Seattle Children's Hospital Genetics Laboratories Seattle Children's
United States
5047
  • D Deletion/duplication analysis

Vascular Anomalies (VANseq) Expanded Sequencing Panel

Seattle Children's Hospital Genetics Laboratories Seattle Children's
United States
5047
  • C Sequence analysis of the entire coding region

GLMN

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

Vascular Malformations Panel

Blueprint Genetics
Finland
714
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CEN4GEN Comprehensive Hereditary Cancer Syndrome: Gene sequencing Panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
1143
  • C Sequence analysis of the entire coding region

GLOMUVENOUS MALFORMATION

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

Glomuvenous malformations

Labor Dr. Wisplinghoff
Germany
11
  • C Sequence analysis of the entire coding region

Vascular Malformation NGS Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
3421
  • C Sequence analysis of the entire coding region

Vascular Malformations NGS Multi-Gene Panel (21 Genes)

Amsterdam UMC Genome Diagnostics Amsterdam University Medical Center
Netherlands
1021
  • C Sequence analysis of the entire coding region

GLMN 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

Venous malformation (TEK, GLMN)

Center for Human Genetics Cliniques Universitaires Saint Luc
Belgium
12
  • C Sequence analysis of the entire coding region

Glomuvenous Malformation (TEK, GLMN)

Center for Human Genetics Cliniques Universitaires Saint Luc
Belgium
12
  • C Sequence analysis of the entire coding region

Blue Rubber Bleb Nevus Syndrome

Laboratory of Human Molecular Genetics de Duve Institute - Universite catholique de Louvain
Belgium
11
  • C Sequence analysis of the entire coding region

Results: 21 to 38 of 38

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.