Clinical and research tests for C1366911 - Genetic Testing Registry (GTR) - NCBI

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Results: 1 to 15 of 15

Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
Cerebral cavernous malformations Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests United States	3	3	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Cerebral cavernous malformations Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States	3	3	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Cerebral cavernous malformations NGS panel HNL Genomics Connective Tissue Gene Tests United States	3	3	C Sequence analysis of the entire coding region T Targeted variant analysis
Vascular malformations Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States	20	19	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Vascular malformations NGS panel HNL Genomics Connective Tissue Gene Tests United States	20	19	C Sequence analysis of the entire coding region T Targeted variant analysis
Vascular malformations Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests United States	20	19	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Cerebral cavernous malformations NGS panel HNL Genomics Connective Tissue Gene Tests United States	3	3	C Sequence analysis of the entire coding region T Targeted variant analysis
Cerebral cavernous malformations Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests United States	3	3	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Cerebral cavernous malformations Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States	3	3	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Hereditary hemorrhagic telangiectasia (HHT) Pittsburgh Cytogenetics Laboratory University of Pittsburgh Medical Center United States	8	9	D Deletion/duplication analysis
Cerebral cavernous malformations: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada	3	3	C Sequence analysis of the entire coding region
Cerebral Cavernous Malformation Panel, Sequencing and Deletion/Duplication ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories United States	4	3	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Cerebral cavernous malformations 1 Labor Dr. Wisplinghoff Germany	1	1	C Sequence analysis of the entire coding region
Invitae Cerebral Cavernous Malformations Panel Invitae United States	4	3	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Vascular Malformations NGS Multi-Gene Panel (21 Genes) Amsterdam UMC Genome Diagnostics Amsterdam University Medical Center, Location AMC Netherlands	10	21	C Sequence analysis of the entire coding region

Results: 1 to 15 of 15

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