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Items: 19

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    Number of Variants: 19

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3885225copy number variation1nstd102humanBenign GRCh37 chr1: 116,226,658-116,232,765 , GRCh38.p12 chr1: 115,684,037-115,690,144 VANGL1
    nsv3886523copy number variation1nstd102humanBenign GRCh37 chr1: 116,227,664-116,232,765 , GRCh38.p12 chr1: 115,685,043-115,690,144 VANGL1
    nsv3887166copy number variation1nstd102humanBenign GRCh37 chr1: 116,230,000-116,234,313 , GRCh38.p12 chr1: 115,687,379-115,691,692 VANGL1
    nsv3876156copy number variation1nstd102humanBenign GRCh37 chr1: 116,228,152-116,231,289 , GRCh38.p12 chr1: 115,685,531-115,688,668 VANGL1
    nsv3881246copy number variation1nstd102humanBenign GRCh37 chr1: 116,229,678-116,232,765 , GRCh38.p12 chr1: 115,687,057-115,690,144 VANGL1
    nsv3878195copy number variation1nstd102humanBenign GRCh37 chr1: 116,232,678-116,296,777 , GRCh38.p12 chr1: 115,690,057-115,754,156 VANGL1, CASQ2
    nsv3882130copy number variation1nstd102humanBenign GRCh37 chr1: 116,234,313-116,295,007 , GRCh38.p12 chr1: 115,691,692-115,752,386 VANGL1, CASQ2
    nsv5381058copy number variation1nstd102humanPathogenic GRCh37 chr1: 102,021,465-119,737,478 , GRCh38.p12 chr1: 101,555,909-119,194,855 VANGL1, AMYP1, 320 more genes
    nsv3877365copy number variation1nstd102humanPathogenic GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250 VANGL1, MARK1, 4930 more genes
    nsv3885206copy number variation1nstd102humanPathogenic GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793 VANGL1, SNAP47, 4927 more genes
    nsv3884414copy number variation2nstd102humanPathogenic GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485 VANGL1, RNU1-153P, 4887 more genes
    nsv3882464copy number variation1nstd102humanPathogenic GRCh37 chr1: 93,837,992-121,343,783 , GRCh38.p12 chr1: 93,372,435-121,601,985 VANGL1, LINC02607, 513 more genes
    nsv3890331copy number variation1nstd102humanPathogenic NCBI36 chr1: 104,669,629-120,321,801 , GRCh37 chr1: 104,868,106-120,471,049 , GRCh38 chr1: 104,325,484-119,977,655 VANGL1, OR11I1P, 324 more genes
    nsv6313671copy number variation1nstd102humanPathogenic GRCh37 chr1: 111,647,582-121,343,783 , GRCh38.p12 chr1: 111,104,960-121,601,985 VANGL1, GAPDHP23, 243 more genes
    nsv3898188copy number variation1nstd102humanPathogenic NCBI36 chr1: 110,100,775-118,994,350 , GRCh38 chr1: 109,756,630-118,650,204 , GRCh37 chr1: 110,299,252-119,192,827 VANGL1, AP4B1-AS1, 198 more genes
    nsv4673999copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 114,024,461-116,189,135 , GRCh38.p12 chr1: 113,481,839-115,646,514 VANGL1, AMPD1, 43 more genes
    nsv4451097copy number variation1nstd102humanUncertain significance GRCh37 chr1: 116,105,961-116,397,171 , GRCh38.p12 chr1: 115,563,340-115,854,550 VANGL1, CASQ2, 4 more genes
    nsv7095740copy number variation1nstd102humanUncertain significance GRCh37 chr1: 113,456,513-116,311,162 , GRCh38.p12 chr1: 112,913,891-115,768,541 VANGL1, TRIM33, 55 more genes
    nsv3873640copy number variation1nstd102humanUncertain significance GRCh37 chr1: 116,065,879-116,693,221 , GRCh38.p12 chr1: 115,523,258-116,150,600 VANGL1, CNOT7P2, 12 more genes
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