U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 164

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5944916copy number variation1nstd209human GRCh38 chr15: 89,908,403-89,909,371 , GRCh37.p13 chr15: 90,451,635-90,452,603 ARPIN-AP3S2, ARPIN
    nsv5712934mobile element insertion1nstd211human GRCh38 chr15: 89,899,461-89,899,461 , GRCh37.p13 chr15: 90,442,693-90,442,693 ARPIN-AP3S2, ARPIN
    nsv5528154copy number variation1nstd206human GRCh38 chr15: 89,908,403-89,909,375 , GRCh37.p13 chr15: 90,451,635-90,452,607 ARPIN, ARPIN-AP3S2
    nsv5423966mobile element insertion1nstd206human GRCh38 chr15: 89,899,461-89,899,512 , GRCh37.p13 chr15: 90,442,693-90,442,744 ARPIN-AP3S2, ARPIN
    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
    nsv5349281translocation1nstd200human GRCh38 chr15: 89,909,375-89,909,375 , GRCh38 chr15: 89,908,403-89,908,403 , GRCh37.p13 chr15: 90,452,607-90,452,607 , GRCh37.p13 chr15: 90,451,635-90,451,635 ARPIN, ARPIN-AP3S2
    nsv5349280translocation1nstd200human GRCh38 chr15: 89,902,347-89,902,347 , GRCh38 chr15: 89,902,290-89,902,290 , GRCh37.p13 chr15: 90,445,522-90,445,522 , GRCh37.p13 chr15: 90,445,579-90,445,579 ARPIN-AP3S2, ARPIN
    nsv5337881translocation1nstd200human GRCh37 chr15: 90,451,635-90,451,635 , GRCh37 chr15: 90,452,607-90,452,607 , GRCh38.p12 chr15: 89,908,403-89,908,403 , GRCh38.p12 chr15: 89,909,375-89,909,375 ARPIN-AP3S2, ARPIN
    nsv5002307copy number variation1nstd200human GRCh38 chr15: 89,906,935-89,907,013 , GRCh37.p13 chr15: 90,450,167-90,450,245 ARPIN, ARPIN-AP3S2
    nsv5002306copy number variation1nstd200human GRCh38 chr15: 89,905,292-89,914,241 , GRCh37.p13 chr15: 90,448,524-90,457,473 ARPIN-AP3S2, ARPIN
    nsv5002305copy number variation1nstd200human GRCh38 chr15: 89,901,871-89,904,341 , GRCh37.p13 chr15: 90,445,103-90,447,573 ARPIN, ARPIN-AP3S2
    nsv4856280copy number variation1nstd200human GRCh37 chr15: 90,448,540-90,457,456 , GRCh38.p12 chr15: 89,905,308-89,914,224 ARPIN, ARPIN-AP3S2
    nsv4856279copy number variation1nstd200human GRCh37 chr15: 90,445,414-90,445,516 , GRCh38.p12 chr15: 89,902,182-89,902,284 ARPIN, ARPIN-AP3S2
    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
    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
    nsv4456244copy number variation2nstd102humanUncertain significance GRCh37 chr15: 90,394,518-90,497,831 , GRCh38.p12 chr15: 89,851,286-89,954,599 AP3S2, LOC100421368, 6 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
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center