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Results: 1 to 20 of 33

Tests names and labsConditionsGenes and analytesMethods

Cerebral cavernous malformations 3 - Sanger / Del Dup Comprehensive

Connective Tissue Gene Tests
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Cerebral cavernous malformations 3 (CCM3) - Deletion/Duplication

Connective Tissue Gene Tests
United States
11
  • D Deletion/duplication analysis

Cerebral cavernous malformations 3 (CCM3) - Sanger Sequencing

Connective Tissue Gene Tests
United States
11
  • C Sequence analysis of the entire coding region

Rapid microarray (CGH and SNP)

Allele Diagnostics
United States
247231
  • H Detection of homozygosity
  • D Deletion/duplication analysis
  • H Detection of homozygosity

CCM2, KRIT1, PDCD10. NextGeneDx. Complete sequencing by NGS

Instituto de Medicina Genomica
Spain
33
  • C Sequence analysis of the entire coding region

Cerebral Cavernous Malformations Sequencing Panel

PreventionGenetics
United States
33
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

KRIT1. Complete sequencing

Instituto de Medicina Genomica
Spain
31
  • C Sequence analysis of the entire coding region

CCM2. Complete sequencing

Instituto de Medicina Genomica
Spain
31
  • C Sequence analysis of the entire coding region

KRIT1. Detection of the mutation c.1363C>T by sequencing

Instituto de Medicina Genomica
Spain
31
  • T Targeted variant analysis

PDCD10. Complete sequencing

Instituto de Medicina Genomica
Spain
31
  • C Sequence analysis of the entire coding region

CCM2, KRIT1, PDCD10. MLPA testing

Instituto de Medicina Genomica
Spain
33
  • D Deletion/duplication analysis

Cerebral Cavernous Malformations via the PDCD10/CCM3 Gene

PreventionGenetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

CEREBRAL CAVERNOUS MALFORMATION, FAMILIAL

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
33
  • C Sequence analysis of the entire coding region

Vascular Malformations NGS Multi-Gene Panel (21 Genes)

DNA Diagnostics Laboratory Academic Medical Centre, University of Amsterdam
Netherlands
1021
  • C Sequence analysis of the entire coding region

Hereditary cerebral cavernous malformation

Bioarray
Spain
11
  • C Sequence analysis of the entire coding region

Cerebral cavernous malformations (NGS panel for 3 genes)

CGC Genetics
Portugal
33
  • C Sequence analysis of the entire coding region

CCM2 Gene Sequencing

GeneDx
United States
11
  • C Sequence analysis of the entire coding region

PDCD10 Gene Sequencing

GeneDx
United States
11
  • C Sequence analysis of the entire coding region

Cerebral Cavernous Malformation: Sequencing Panel

Emory Genetics Laboratory Emory University
United States
33
  • C Sequence analysis of the entire coding region

Cerebral Cavernous Malformation (CCM) Sequencing, 3 Genes

ARUP Laboratories, Molecular Genetics University of Utah ARUP Lab
United States
43
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 33

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.