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Items: 1 to 20 of 209

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7017615copy number variation1nstd229human GRCh38 chr19: 29,529,144-29,536,708 , GRCh37.p13 chr19: 30,020,051-30,027,615 VSTM2B
    nsv7013119copy number variation1nstd229human GRCh38 chr19: 29,546,810-29,549,066 , GRCh37.p13 chr19: 30,037,717-30,039,973 VSTM2B
    nsv7012247copy number variation1nstd229human GRCh38 chr19: 29,520,756-29,524,938 , GRCh37.p13 chr19: 30,011,663-30,015,845 VSTM2B, VSTM2B-DT
    nsv7009327copy number variation1nstd229human GRCh38 chr19: 29,549,115-29,552,489 , GRCh37.p13 chr19: 30,040,022-30,043,396 VSTM2B
    nsv7000983copy number variation1nstd229human GRCh38 chr19: 29,535,501-29,588,500 , GRCh37.p13 chr19: 30,026,408-30,079,407 VSTM2B
    nsv7000412copy number variation1nstd229human GRCh38 chr19: 29,541,747-29,541,936 , GRCh37.p13 chr19: 30,032,654-30,032,843 VSTM2B
    nsv6999105copy number variation1nstd229human GRCh38 chr19: 29,559,674-29,559,769 , GRCh37.p13 chr19: 30,050,581-30,050,676 VSTM2B
    nsv6534466copy number variation1nstd223human GRCh38 chr19: 29,520,756-29,524,938 , GRCh37.p13 chr19: 30,011,663-30,015,845 VSTM2B-DT, VSTM2B
    nsv6527526copy number variation1nstd223human GRCh38 chr19: 28,925,173-32,768,942 , GRCh37.p13 chr19: 29,416,080-33,259,848 DPY19L3, CCNE1, 50 more genes
    nsv6526233copy number variation1nstd223human GRCh38 chr19: 28,377,231-29,769,380 , GRCh37.p13 chr19: 28,868,138-30,260,287 LINC01532, C19orf12, 16 more genes
    nsv6290300copy number variation1nstd102humanPathogenic GRCh37 chr19: 19,546,923-41,313,229 , GRCh38.p12 chr19: 19,436,114-40,807,324 ZNF420, LOC105372330, 574 more genes
    nsv6288639insertion1nstd214human GRCh38 chr19: 29,537,703-29,537,703 , GRCh37.p13 chr19: 30,028,610-30,028,610 VSTM2B
    nsv6108022insertion1nstd212human GRCh38 chr19: 29,537,712-29,537,712 , GRCh37.p13 chr19: 30,028,619-30,028,619 VSTM2B
    nsv5927788copy number variation1nstd209human GRCh38 chr19: 29,559,674-29,559,768 , GRCh37.p13 chr19: 30,050,581-30,050,675 VSTM2B
    nsv5875137copy number variation1nstd209human GRCh38 chr19: 29,551,147-29,553,196 , GRCh37.p13 chr19: 30,042,054-30,044,103 VSTM2B
    nsv5663054insertion1nstd207human GRCh38 chr19: 29,542,690-29,542,690 , GRCh37.p13 chr19: 30,033,597-30,033,597 VSTM2B
    nsv5661762insertion1nstd207human GRCh38 chr19: 29,537,703-29,537,703 , GRCh37.p13 chr19: 30,028,610-30,028,610 VSTM2B
    nsv5531422copy number variation1nstd206human GRCh38 chr19: 29,534,712-29,534,851 , GRCh37.p13 chr19: 30,025,619-30,025,758 VSTM2B
    nsv5359697translocation1nstd200human GRCh38 chr19: 29,559,769-29,559,769 , GRCh38 chr19: 29,559,678-29,559,678 , GRCh37.p13 chr19: 30,050,676-30,050,676 , GRCh37.p13 chr19: 30,050,585-30,050,585 VSTM2B
    nsv5321302copy number variation1nstd204human GRCh38.p13 chr19: 29,534,171-29,534,282 , GRCh37.p13 chr19: 30,025,078-30,025,189 VSTM2B
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