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Items: 1 to 20 of 197

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv4856291copy number variation1nstd200human GRCh37 chr15: 90,639,311-90,639,915 , GRCh38.p12 chr15: 90,096,079-90,096,683 IDH2
    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
    nsv4675805copy number variation1nstd102humanUncertain significance GRCh37 chr15: 90,111,672-90,671,886 , GRCh38.p12 chr15: 89,568,441-90,128,654 RNU6-132P, PEX11A, 23 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
    nsv4621277copy number variation1nstd183human GRCh37 chr15: 90,645,621-90,645,778 , GRCh38.p12 chr15: 90,102,389-90,102,546 IDH2, IDH2-DT
    nsv4456430copy number variation1nstd102humanPathogenic GRCh37 chr15: 90,288,175-102,429,112 , GRCh38.p12 chr15: 89,744,944-101,888,909 IQGAP1, LOC400464, 210 more genes
    nsv4423538copy number variation1nstd174human GRCh37 chr15: 90,632,610-90,842,193 , GRCh38.p12 chr15: 90,089,378-90,298,961 NGRN, GDPGP1, 10 more genes
    nsv4385824copy number variation1nstd173human GRCh37 chr15: 90,250,919-91,461,024 , GRCh38.p12 chr15: 89,707,688-90,917,794 , LOC100631255, 44 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
    nsv4375224copy number variation1nstd173human GRCh37 chr15: 90,246,823-91,461,537 , GRCh38.p12 chr15: 89,703,592-90,918,307 , RNU6-1111P, 44 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
    nsv4234626copy number variation1nstd166human GRCh37.p13 chr15: 90,639,296-90,639,885 , GRCh38.p12 chr15: 90,096,064-90,096,653 IDH2
    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
    nsv3921462copy number variation1nstd102humanUncertain significance NCBI36 chr15: 87,527,741-88,772,110 , GRCh37.p13 chr15: 89,726,737-90,971,106 , GRCh38.p12 chr15: 89,183,506-90,427,874 LOC100631255, RN7SL736P, 51 more genes
    nsv3920826copy number variation1nstd102humanLikely benign GRCh37 chr15: 90,364,376-90,759,821 , NCBI36 chr15: 88,165,380-88,560,825 , GRCh38 chr15: 89,821,144-90,216,589 RPS12P26, RNU6-1111P, 15 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
    nsv3920248copy number variation1nstd102humanPathogenic NCBI36 chr15: 87,618,716-100,262,146 , GRCh37.p13 chr15: 89,817,712-102,444,623 , GRCh38.p12 chr15: 89,274,481-101,904,420 FAM149B1P1, MIR9-3HG, 229 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
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