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Items: 1 to 20 of 109

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5523495copy number variation1nstd206human GRCh38 chr15: 87,553,175-87,606,574 , GRCh37.p13 chr15: 88,096,406-88,149,805 LINC00052
    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
    nsv5140783mobile element insertion1nstd203human GRCh38 chr15: 87,578,833-87,578,847 , GRCh37.p13 chr15: 88,122,064-88,122,078 LINC00052
    nsv5009139copy number variation1nstd200human GRCh38 chr15: 87,553,175-87,606,574 , GRCh37.p13 chr15: 88,096,406-88,149,805 LINC00052
    nsv5002225copy number variation1nstd200human GRCh38 chr15: 87,569,730-87,583,729 , GRCh37.p13 chr15: 88,112,961-88,126,960 LINC00052
    nsv4856215copy number variation1nstd200human GRCh37 chr15: 88,112,961-88,126,960 , GRCh38.p12 chr15: 87,569,730-87,583,729 LINC00052
    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
    nsv4377776copy number variation1nstd173human GRCh37 chr15: 86,980,083-93,499,239 , GRCh38.p12 chr15: 86,436,852-92,956,009 , RNU6-1111P, 136 more genes
    nsv4350274copy number variation1nstd102humanPathogenic GRCh37 chr15: 83,883,823-92,165,844 , GRCh38.p12 chr15: 83,215,071-91,622,614 AKAP13, LOC105370972, 184 more genes
    nsv4238600copy number variation1nstd166human GRCh37.p13 chr15: 88,115,829-88,637,773 , GRCh38.p12 chr15: 87,572,598-88,094,542 LINC00052, MIR11181, 1 more genes
    nsv4237151copy number variation1nstd166human GRCh37.p13 chr15: 88,120,140-88,126,109 , GRCh38.p12 chr15: 87,576,909-87,582,878 LINC00052
    nsv3922157copy number variation1nstd102humanUncertain significance NCBI36 chr15: 29,852,369-100,338,915 , GRCh37.p13 chr15: 32,065,077-102,521,392 , GRCh38.p12 chr15: 31,772,874-101,981,189 GCHFR, SPPL2A, 1382 more genes
    nsv3920352copy number variation1nstd102humanPathogenic GRCh38 chr15: 83,711,377-101,843,270 , NCBI36 chr15: 82,171,133-100,200,996 , GRCh37 chr15: 84,380,129-102,383,473 LOC102724465, SNRPA1, 333 more genes
    nsv3919468copy number variation1nstd102humanPathogenic NCBI36 chr15: 26,996,912-100,338,915 , GRCh37.p13 chr15: 29,209,620-102,521,392 , GRCh38.p12 chr15: 28,917,417-101,981,189 RNU6-18P, GOLGA8K, 1442 more genes
    nsv3919393copy number variation1nstd102humanPathogenic NCBI36 chr15: 84,170,900-100,278,724 , GRCh37 chr15: 86,369,896-102,461,201 , GRCh38 chr15: 85,826,665-101,920,998 LOC105370997, LOC102724465, 270 more genes
    nsv3918992copy number variation1nstd102humanPathogenic NCBI36 chr15: 75,141,730-95,931,047 , GRCh37.p13 chr15: 77,354,675-98,130,043 , GRCh38.p12 chr15: 77,062,333-97,586,813 TLNRD1, FES, 403 more genes
    nsv3918770copy number variation1nstd102humanUncertain significance NCBI36 chr15: 20,280,728-100,338,915 , GRCh37.p13 chr15: 22,729,364-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189 SNRPCP18, SNORD116-30, 1622 more genes
    nsv3918644copy number variation1nstd102humanUncertain significance NCBI36 chr15: 20,313,935-100,338,915 , GRCh37.p13 chr15: 22,762,571-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189 SNORD116-23, UBE2Q2P6, 1622 more genes
    nsv3917589copy number variation1nstd102humanPathogenic GRCh37 chr15: 60,120,659-102,461,201 , GRCh38 chr15: 59,828,460-101,920,998 , NCBI36 chr15: 57,907,951-100,278,724 GAPDHP61, SNORD18B, 840 more genes
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