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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6131617insertion1nstd186human GRCh37 chr15: 81,205,870-81,205,872 , GRCh38.p12 chr15: 80,913,529-80,913,531 CEMIP
    nsv5970529insertion1nstd209human GRCh38 chr15: 80,913,530-80,913,530 , GRCh37.p13 chr15: 81,205,871-81,205,871 CEMIP
    nsv5935349copy number variation1nstd209human GRCh38 chr15: 77,970,674-82,312,707 , GRCh37.p13 chr15: 78,263,016-82,605,043 , ST20, 91 more genes
    nsv5930438copy number variation1nstd209human GRCh38 chr15: 80,912,036-80,913,530 , GRCh37.p13 chr15: 81,204,377-81,205,871 , CEMIP
    nsv5930205copy number variation1nstd209human GRCh38 chr15: 80,911,976-80,913,524 , GRCh37.p13 chr15: 81,204,317-81,205,865 , CEMIP
    nsv5849087copy number variation1nstd209human GRCh38 chr15: 80,884,145-80,886,244 , GRCh37.p13 chr15: 81,176,486-81,178,585 CEMIP
    nsv5706700mobile element insertion2nstd211human GRCh38 chr15: 80,872,475-80,872,475 , GRCh37.p13 chr15: 81,164,816-81,164,816 CEMIP
    nsv5659297insertion1nstd207human GRCh38 chr15: 80,913,529-80,913,529 , GRCh37.p13 chr15: 81,205,870-81,205,870 CEMIP
    nsv5656080insertion1nstd207human GRCh38 chr15: 80,872,459-80,872,459 , GRCh37.p13 chr15: 81,164,800-81,164,800 CEMIP
    nsv5646858insertion1nstd207human GRCh38 chr15: 80,911,950-80,911,950 , GRCh37.p13 chr15: 81,204,291-81,204,291 , CEMIP
    nsv5542791insertion1nstd206human GRCh38 chr15: 80,913,529-80,913,531 , GRCh37.p13 chr15: 81,205,870-81,205,872 CEMIP
    nsv5529284copy number variation1nstd206human GRCh38 chr15: 80,926,978-80,927,093 , GRCh37.p13 chr15: 81,219,319-81,219,434 CEMIP
    nsv5520947copy number variation1nstd206human GRCh38 chr15: 80,789,530-80,792,880 , GRCh37.p13 chr15: 81,081,871-81,085,221 CEMIP
    nsv5518297copy number variation1nstd206human GRCh38 chr15: 80,781,152-80,785,557 , GRCh37.p13 chr15: 81,073,493-81,077,898 CEMIP
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5349218translocation1nstd200human GRCh38 chr15: 80,831,387-80,831,387 , GRCh38 chr15: 80,831,457-80,831,457 , GRCh37.p13 chr15: 81,123,728-81,123,728 , GRCh37.p13 chr15: 81,123,798-81,123,798 CEMIP
    nsv5313826copy number variation1nstd204human GRCh38.p13 chr15: 80,798,428-80,800,066 , GRCh37.p13 chr15: 81,090,769-81,092,407 CEMIP
    nsv5158252mobile element insertion1nstd203human GRCh38 chr15: 80,872,459-80,872,475 , GRCh37.p13 chr15: 81,164,800-81,164,816 CEMIP
    nsv5147198mobile element insertion1nstd203human GRCh38 chr15: 80,872,464-80,872,475 , GRCh37.p13 chr15: 81,164,805-81,164,816 CEMIP
    nsv5009098copy number variation1nstd200human GRCh38 chr15: 80,898,945-80,901,610 , GRCh37.p13 chr15: 81,191,286-81,193,951 , CEMIP
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