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Items: 1 to 20 of 134

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6131053insertion1nstd186human GRCh37 chr17: 76,163,788-76,163,788 , GRCh38.p12 chr17: 78,167,707-78,167,707 SYNGR2
    nsv5979945insertion1nstd209human GRCh38 chr17: 78,167,707-78,167,707 , GRCh37.p13 chr17: 76,163,788-76,163,788 SYNGR2
    nsv5662993insertion1nstd207human GRCh38 chr17: 78,167,707-78,167,707 , GRCh37.p13 chr17: 76,163,788-76,163,788 SYNGR2
    nsv5552677insertion1nstd206human GRCh38 chr17: 78,167,707-78,167,707 , GRCh37.p13 chr17: 76,163,788-76,163,788 SYNGR2
    nsv5530798copy number variation1nstd206human GRCh38 chr17: 78,167,662-78,167,987 , GRCh37.p13 chr17: 76,163,743-76,164,068 SYNGR2
    nsv5526575copy number variation1nstd206human GRCh38 chr17: 78,173,173-78,173,313 , GRCh37.p13 chr17: 76,169,254-76,169,394 , SYNGR2, 1 more genes
    nsv5155861mobile element insertion1nstd203human GRCh38 chr17: 78,167,552-78,167,588 , GRCh37.p13 chr17: 76,163,633-76,163,669 SYNGR2
    nsv5149880mobile element insertion1nstd203human GRCh38 chr17: 78,167,707-78,167,719 , GRCh37.p13 chr17: 76,163,788-76,163,800 SYNGR2
    nsv5148597mobile element insertion1nstd203human GRCh38 chr17: 78,167,706-78,167,719 , GRCh37.p13 chr17: 76,163,787-76,163,800 SYNGR2
    nsv5035778inversion1nstd200human GRCh38 chr17: 78,138,562-78,604,810 , GRCh37.p13 chr17: 76,134,643-76,600,892 , DNAH17-AS1, 20 more genes
    nsv4676104copy number variation1nstd102humanPathogenic GRCh37 chr17: 73,261,871-78,608,763 , GRCh38.p12 chr17: 75,265,790-80,634,963 LLGL2, TSEN54, 165 more genes
    nsv4457646copy number variation1nstd102humanPathogenic GRCh37 chr17: 62,778,720-81,041,938 , GRCh38.p12 chr17: 64,782,602-83,084,062 LOC107985089, ARSG, 448 more genes
    nsv4259276copy number variation1nstd166human GRCh37.p13 chr17: 76,092,239-76,465,993 , GRCh38.p12 chr17: 78,096,158-78,469,911 , SYNGR2, 19 more genes
    nsv3919635copy number variation1nstd102humanPathogenic GRCh37 chr17: 76,088,317-81,044,553 , NCBI36 chr17: 73,599,912-78,637,842 , GRCh38 chr17: 78,092,236-83,086,677 LINC03048, MIR3186, 154 more genes
    nsv3919156copy number variation1nstd102humanPathogenic GRCh38 chr17: 69,916,435-83,102,552 , GRCh37 chr17: 67,912,576-81,048,189 , NCBI36 chr17: 65,424,171-78,653,717 CD300A, RNF213, 359 more genes
    nsv3917654copy number variation1nstd102humanPathogenic NCBI36 chr17: 64,716,815-78,637,842 , GRCh37 chr17: 67,205,220-81,044,553 , GRCh38 chr17: 69,209,079-83,086,677 LOC101928447, GRB2, 368 more genes
    nsv3914783copy number variation1nstd102humanPathogenic NCBI36 chr17: 16,698,288-78,654,742 , GRCh37.p13 chr17: 16,757,563-81,048,189 , GRCh38.p12 chr17: 16,854,249-83,103,577 LOC105371922, GJD3, 1855 more genes
    nsv3911899copy number variation1nstd102humanLikely benign GRCh38 chr17: 78,092,356-78,444,214 , NCBI36 chr17: 73,600,032-73,951,891 , GRCh37 chr17: 76,088,437-76,440,296 SOCS3, DNAH17, 17 more genes
    nsv3911811copy number variation1nstd102humanPathogenic NCBI36 chr17: 31,824,931-78,654,742 , GRCh37.p13 chr17: 34,750,818-81,048,189 , GRCh38.p12 chr17: 36,382,248-83,103,577 PRPSAP1, CACNG1, 1350 more genes
    nsv3909523copy number variation1nstd102humanPathogenic GRCh37 chr17: 63,689,671-81,041,938 , GRCh38.p12 chr17: 65,693,553-83,084,062 RPL38, RNF157-AS1, 428 more genes
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