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 412

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5961205insertion1nstd209human GRCh38 chr9: 23,704,136-23,704,136 , GRCh37.p13 chr9: 23,704,134-23,704,134 ELAVL2
    nsv5956672insertion1nstd209human GRCh38 chr9: 23,786,802-23,786,802 , GRCh37.p13 chr9: 23,786,800-23,786,800 ELAVL2
    nsv5954723insertion1nstd209human GRCh38 chr9: 23,735,105-23,735,105 , GRCh37.p13 chr9: 23,735,103-23,735,103 ELAVL2
    nsv5914816copy number variation1nstd209human GRCh38 chr9: 21,981,197-25,406,892 , GRCh37.p13 chr9: 21,981,196-25,406,890 , CLIC4P1, 20 more genes
    nsv5719662mobile element insertion1nstd211human GRCh38 chr9: 23,782,404-23,782,404 , GRCh37.p13 chr9: 23,782,402-23,782,402 ELAVL2
    nsv5711536mobile element insertion2nstd211human GRCh38 chr9: 23,802,895-23,802,895 , GRCh37.p13 chr9: 23,802,893-23,802,893 ELAVL2
    nsv5704699mobile element insertion1nstd211human GRCh38 chr9: 23,778,231-23,778,231 , GRCh37.p13 chr9: 23,778,229-23,778,229 ELAVL2
    nsv5699067mobile element insertion2nstd211human GRCh38 chr9: 23,746,012-23,746,012 , GRCh37.p13 chr9: 23,746,010-23,746,010 ELAVL2
    nsv5637732insertion1nstd207human GRCh38 chr9: 23,704,136-23,704,136 , GRCh37.p13 chr9: 23,704,134-23,704,134 ELAVL2
    nsv5553260insertion1nstd206human GRCh38 chr9: 23,704,151-23,704,187 , GRCh37.p13 chr9: 23,704,149-23,704,185 ELAVL2
    nsv5491531copy number variation1nstd206human GRCh38 chr9: 23,720,080-23,720,434 , GRCh37.p13 chr9: 23,720,078-23,720,432 ELAVL2
    nsv5410407mobile element insertion1nstd206human GRCh38 chr9: 23,746,012-23,746,063 , GRCh37.p13 chr9: 23,746,010-23,746,061 ELAVL2
    nsv5409832mobile element insertion1nstd206human GRCh38 chr9: 23,802,895-23,802,946 , GRCh37.p13 chr9: 23,802,893-23,802,944 ELAVL2
    nsv5400332mobile element insertion1nstd206human GRCh38 chr9: 23,778,231-23,778,282 , GRCh37.p13 chr9: 23,778,229-23,778,280 ELAVL2
    nsv5311622copy number variation1nstd204human GRCh38.p13 chr9: 23,698,548-23,699,972 , GRCh37.p13 chr9: 23,698,546-23,699,970 ELAVL2
    nsv5301963copy number variation1nstd204human GRCh38.p13 chr9: 23,801,831-23,802,994 , GRCh37.p13 chr9: 23,801,829-23,802,992 ELAVL2
    nsv5248066copy number variation1nstd204human GRCh38.p13 chr9: 23,832,001-23,835,100 , GRCh37.p13 chr9: 23,831,999-23,835,098 ELAVL2
    nsv5214228mobile element deletion1nstd204human GRCh38.p13 chr9: 23,783,904-23,784,220 , GRCh37.p13 chr9: 23,783,902-23,784,218 ELAVL2
    nsv5118295mobile element insertion1nstd203human GRCh38 chr9: 23,745,997-23,746,012 , GRCh37.p13 chr9: 23,745,995-23,746,010 ELAVL2
    nsv5118070mobile element insertion1nstd203human GRCh38 chr9: 23,849,569-23,849,581 , GRCh37.p13 chr9: 23,849,567-23,849,579 LOC105375993, ELAVL2
    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