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Items: 1 to 20 of 134

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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
    nsv5009159copy number variation1nstd200human GRCh38 chr15: 89,849,520-89,851,727 , GRCh37.p13 chr15: 90,392,752-90,394,959 ARPIN-AP3S2, AP3S2, 1 more genes
    nsv4863952copy number variation1nstd200human GRCh37 chr15: 90,392,784-90,394,912 , GRCh38.p12 chr15: 89,849,552-89,851,680 ARPIN-AP3S2, AP3S2, 1 more genes
    nsv4856277copy number variation1nstd200human GRCh37 chr15: 90,391,779-90,392,759 , GRCh38.p12 chr15: 89,848,547-89,849,527 ARPIN-AP3S2, AP3S2, 1 more genes
    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
    nsv4633183copy number variation1nstd183human GRCh37 chr15: 90,390,177-90,394,860 , GRCh38.p12 chr15: 89,846,945-89,851,628 AP3S2, MIR5094, 1 more genes
    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
    nsv4242676copy number variation1nstd166human GRCh37.p13 chr15: 90,386,744-90,396,067 , GRCh38.p12 chr15: 89,843,512-89,852,835 AP3S2, MIR5094, 1 more genes
    nsv4237237copy number variation1nstd166human GRCh37.p13 chr15: 90,390,056-90,392,850 , GRCh38.p12 chr15: 89,846,824-89,849,618 AP3S2, ARPIN-AP3S2, 1 more genes
    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
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