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Items: 1 to 20 of 180

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5712011mobile element insertion2nstd211human GRCh38 chr15: 88,617,105-88,617,105 , GRCh37.p13 chr15: 89,160,336-89,160,336 AEN
    nsv5515618copy number variation1nstd206human GRCh38 chr15: 88,628,462-88,628,556 , GRCh37.p13 chr15: 89,171,693-89,171,787 AEN
    nsv5515154copy number variation1nstd206human GRCh38 chr15: 88,627,913-88,628,028 , GRCh37.p13 chr15: 89,171,144-89,171,259 AEN
    nsv5424166mobile element insertion1nstd206human GRCh38 chr15: 88,617,105-88,617,156 , GRCh37.p13 chr15: 89,160,336-89,160,387 AEN
    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
    nsv5373272translocation1nstd200human GRCh38 chr1: 203,861,848-203,861,848 , GRCh38 chr15: 88,616,582-88,616,582 , GRCh37.p13 chr15: 89,159,813-89,159,813 , GRCh37.p13 chr1: 203,830,976-203,830,976 SNRPE, AEN
    nsv5150634mobile element insertion1nstd203human GRCh38 chr15: 88,617,088-88,617,105 , GRCh37.p13 chr15: 89,160,319-89,160,336 AEN
    nsv5009145copy number variation1nstd200human GRCh38 chr15: 88,625,152-88,641,502 , GRCh37.p13 chr15: 89,168,383-89,184,733 AEN, ISG20
    nsv5002257copy number variation1nstd200human GRCh38 chr15: 88,627,913-88,628,028 , GRCh37.p13 chr15: 89,171,144-89,171,259 AEN
    nsv5002256copy number variation1nstd200human GRCh38 chr15: 88,615,682-88,620,985 , GRCh37.p13 chr15: 89,158,913-89,164,216 AEN
    nsv5002255copy number variation1nstd200human GRCh38 chr15: 88,615,158-88,620,656 , GRCh37.p13 chr15: 89,158,389-89,163,887 AEN
    nsv5002254copy number variation1nstd200human GRCh38 chr15: 88,615,155-88,616,347 , GRCh37.p13 chr15: 89,158,386-89,159,578 AEN
    nsv5002253copy number variation1nstd200human GRCh38 chr15: 88,600,845-88,603,231 , GRCh37.p13 chr15: 89,144,076-89,146,462 AEN, LINC01586
    nsv4856234copy number variation1nstd200human GRCh37 chr15: 89,171,144-89,171,259 , GRCh38.p12 chr15: 88,627,913-88,628,028 AEN
    nsv4856233copy number variation1nstd200human GRCh37 chr15: 89,158,913-89,164,216 , GRCh38.p12 chr15: 88,615,682-88,620,985 AEN
    nsv4856232copy number variation1nstd200human GRCh37 chr15: 89,158,389-89,163,887 , GRCh38.p12 chr15: 88,615,158-88,620,656 AEN
    nsv4729092copy number variation1nstd102humanPathogenic GRCh37 chr15: 86,962,053-102,531,392 , GRCh38.p12 chr15: 86,418,822-101,981,189 CHD2, MIR11181, 272 more genes
    nsv4675149copy number variation1nstd102humanPathogenic GRCh37 chr15: 87,189,245-102,429,112 , GRCh38.p12 chr15: 86,646,014-101,888,909 TTLL13, LINC00052, 264 more genes
    nsv4625274copy number variation1nstd183human GRCh37 chr15: 89,169,494-89,183,054 , GRCh38.p12 chr15: 88,626,263-88,639,823 ISG20, AEN
    nsv4577364mobile element insertion1nstd166human GRCh37.p13 chr15: 89,147,166-89,147,166 , GRCh38.p12 chr15: 88,603,935-88,603,935 AEN, LINC01586
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