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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5516451copy number variation1nstd206human GRCh38 chr15: 89,810,546-89,811,641 , GRCh37.p13 chr15: 90,353,777-90,354,872 ANPEP
    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
    nsv5002302copy number variation1nstd200human GRCh38 chr15: 89,810,569-89,811,618 , GRCh37.p13 chr15: 90,353,800-90,354,849 ANPEP
    nsv4856276copy number variation1nstd200human GRCh37 chr15: 90,353,800-90,354,849 , GRCh38.p12 chr15: 89,810,569-89,811,618 ANPEP
    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
    nsv4679244copy number variation1nstd189human GRCh37.p13 chr15: 89,903,203-90,447,762 , GRCh38.p12 chr15: 89,359,972-89,904,530 , ANPEP, 26 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
    nsv4539562insertion1nstd166human GRCh37.p13 chr15: 90,343,122-90,343,122 , GRCh38.p12 chr15: 89,799,891-89,799,891 ANPEP
    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
    nsv4455646copy number variation1nstd102humanUncertain significance GRCh37 chr15: 90,308,996-90,502,529 , GRCh38.p12 chr15: 89,765,765-89,959,297 ARPIN, LOC100421368, 9 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
    nsv4344500sequence alteration1nstd166human GRCh38.p12 chr15: 89,771,606-89,857,148 , GRCh37.p13 chr15: 90,314,837-90,400,380 , ANPEP, 4 more genes
    nsv4250546copy number variation1nstd166human GRCh37.p13 chr15: 90,353,800-90,354,849 , GRCh38.p12 chr15: 89,810,569-89,811,618 ANPEP
    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
    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
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