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 1092

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5906917copy number variation1nstd209human GRCh38 chr5: 21,489,934-21,497,037 , GRCh37.p13 chr5: 21,490,043-21,497,146 GUSBP1
    nsv5903119copy number variation1nstd209human GRCh38 chr5: 21,582,132-21,587,011 , GRCh37.p13 chr5: 21,582,241-21,587,120 GUSBP1
    nsv5900333copy number variation1nstd209human GRCh38 chr5: 21,460,559-21,461,398 , GRCh37.p13 chr5: 21,460,668-21,461,507 GUSBP1
    nsv5893808copy number variation1nstd209human GRCh38 chr5: 21,532,351-21,539,501 , GRCh37.p13 chr5: 21,532,460-21,539,610 GUSBP1
    nsv5892613copy number variation1nstd209human GRCh38 chr5: 21,481,424-21,481,592 , GRCh37.p13 chr5: 21,481,533-21,481,701 GUSBP1
    nsv5842615copy number variation2nstd209human GRCh38 chr5: 21,582,657-21,584,156 , GRCh37.p13 chr5: 21,582,766-21,584,265 GUSBP1
    nsv5842614copy number variation1nstd209human GRCh38 chr5: 21,558,409-21,560,997 , GRCh37.p13 chr5: 21,558,518-21,561,106 GUSBP1
    nsv5842613copy number variation1nstd209human GRCh38 chr5: 21,550,066-21,569,888 , GRCh37.p13 chr5: 21,550,175-21,569,997 GUSBP1
    nsv5842612copy number variation1nstd209human GRCh38 chr5: 21,530,749-21,539,681 , GRCh37.p13 chr5: 21,530,858-21,539,790 GUSBP1
    nsv5842301copy number variation2nstd209human GRCh38 chr5: 21,554,333-21,556,300 , GRCh37.p13 chr5: 21,554,442-21,556,409 GUSBP1
    nsv5842300copy number variation1nstd209human GRCh38 chr5: 21,530,649-21,532,489 , GRCh37.p13 chr5: 21,530,758-21,532,598 GUSBP1
    nsv5842299copy number variation1nstd209human GRCh38 chr5: 21,523,945-21,525,711 , GRCh37.p13 chr5: 21,524,054-21,525,820 GUSBP1
    nsv5842298copy number variation1nstd209human GRCh38 chr5: 21,506,801-21,521,723 , GRCh37.p13 chr5: 21,506,910-21,521,832 GUSBP1
    nsv5842007copy number variation1nstd209human GRCh38 chr5: 21,582,357-21,586,956 , GRCh37.p13 chr5: 21,582,466-21,587,065 GUSBP1
    nsv5842006copy number variation2nstd209human GRCh38 chr5: 21,554,995-21,556,578 , GRCh37.p13 chr5: 21,555,104-21,556,687 GUSBP1
    nsv5722730mobile element insertion1nstd211human GRCh38 chr5: 21,578,016-21,578,016 , GRCh37.p13 chr5: 21,578,125-21,578,125 GUSBP1
    nsv5692145mobile element insertion1nstd211human GRCh38 chr5: 21,468,616-21,468,616 , GRCh37.p13 chr5: 21,468,725-21,468,725 GUSBP1
    nsv5683364mobile element insertion1nstd211human GRCh38 chr5: 21,514,111-21,514,111 , GRCh37.p13 chr5: 21,514,220-21,514,220 GUSBP1
    nsv5674754mobile element insertion1nstd211human GRCh38 chr5: 21,468,595-21,468,595 , GRCh37.p13 chr5: 21,468,704-21,468,704 GUSBP1
    nsv5665482inversion1nstd207human GRCh37.p13 chr5: 21,479,415-21,500,835 , GRCh38 chr5: 21,479,306-21,500,726 GUSBP1
    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