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Results: 1 to 20 of 68

Tests names and labsConditionsGenes, analytes, and microbesMethods

NOTCH3 Gene, Full Gene Analysis

Mayo Clinic Laboratories Mayo Clinic
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

MVL Vision Panel

Molecular Vision Laboratory
United States
13581028
  • C Sequence analysis of the entire coding region

NOTCH3 - MLPA

Centogene AG - the Rare Disease Company
Germany
31
  • D Deletion/duplication analysis

NOTCH3 - Sanger sequencing

Centogene AG - the Rare Disease Company
Germany
31
  • C Sequence analysis of the entire coding region

Stroke, Cerebral Hemorrhage, Hemiplegia, and Migraine Panel

PreventionGenetics, part of Exact Sciences
United States
346160
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Invitae Hereditary Cerebral Small Vessel Disease Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
2410
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Cerebral arteriopathy with subcortical infarcts and leukoencephalopathy 1, 125310, Autosomal dominant; CADASIL1 (CADASIL) (MLPA)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • D Deletion/duplication analysis

Cerebral arteriopathy with subcortical infarcts and leukoencephalopathy 1, 125310, Autosomal dominant; CADASIL1 (CADASIL) (NOTCH3 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

Cerebral Small Vessel Disease Panel

PreventionGenetics, part of Exact Sciences
United States
1310
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Leukodystrophy and Leukoencephalopathy, Adult Onset Panel

PreventionGenetics, part of Exact Sciences
United States
6745
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Cerebral arteriopathy, with subcortical infarcts and leukoencephalopathy 1 Deletion / Duplication test

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

Cerebral arteriopathy, with subcortical infarcts and leukoencephalopathy 1 Comprehensive test

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

Cerebral arteriopathy, with subcortical infarcts and leukoencephalopathy 1 NGS test

HNL Genomics Connective Tissue Gene Tests
United States
11
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Cerebral small vessel disease NGS panel

HNL Genomics Connective Tissue Gene Tests
United States
87
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

CADASIL NGS panel

HNL Genomics Connective Tissue Gene Tests
United States
32
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Cerebral small vessel disease Deletion / Duplication panel

HNL Genomics Connective Tissue Gene Tests
United States
87
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CADASIL Comprehensive panel

HNL Genomics Connective Tissue Gene Tests
United States
32
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

CADASIL Deletion / Duplication panel

HNL Genomics Connective Tissue Gene Tests
United States
32
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Cerebral small vessel disease Comprehensive panel

HNL Genomics Connective Tissue Gene Tests
United States
87
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Next Generation Sequencing for FHM, EA1, EA2, SCA6, CADASIL, CARASIL, COL4A1/2, Fabry Disease, Small Vessel Disease, Epilepsy

Genomics Research Centre Diagnostics Clinic Queensland Unstitute of Technology
Australia
1812
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 68

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.