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 922

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145822copy number variation1nstd232human GRCh37.p13 chr12: 3,204,665-3,204,793 , GRCh38.p12 chr12: 3,095,499-3,095,627 TSPAN9
    nsv7145231copy number variation1nstd232human GRCh37.p13 chr12: 3,307,803-3,307,889 , GRCh38.p12 chr12: 3,198,637-3,198,723 TSPAN9
    nsv7098813copy number variation1nstd102humanPathogenic GRCh37 chr12: 176,047-34,179,852 , GRCh38.p12 chr12: 66,881-34,026,917 TDGP1, RPS4XP14, 680 more genes
    nsv7072562inversion1nstd229human GRCh38 chr12: 2,987,123-3,378,997 , GRCh37.p13 chr12: 3,096,289-3,488,163 RPS27P3, LOC100128253, 6 more genes
    nsv7071757inversion1nstd229human GRCh38 chr12: 2,390,179-3,608,024 , GRCh37.p13 chr12: 2,499,345-3,717,190 THCAT155, TSPAN9, 28 more genes
    nsv7068624inversion1nstd229human GRCh38 chr12: 2,500,360-5,372,895 , GRCh37.p13 chr12: 2,609,526-5,482,061 LOC105369607, IQSEC3P1, 62 more genes
    nsv7065938inversion1nstd229human GRCh38 chr12: 3,212,752-3,477,293 , GRCh37.p13 chr12: 3,321,918-3,586,459 RPS26P44, LINC02417, 6 more genes
    nsv7060482inversion1nstd229human GRCh38 chr12: 3,195,609-3,203,232 , GRCh37.p13 chr12: 3,304,775-3,312,398 TSPAN9
    nsv6917896copy number variation1nstd229human GRCh38 chr12: 3,062,301-3,094,000 , GRCh37.p13 chr12: 3,171,467-3,203,166 TSPAN9, RPL13AP24
    nsv6917197copy number variation1nstd229human GRCh38 chr12: 3,249,051-3,251,575 , GRCh37.p13 chr12: 3,358,217-3,360,741 TSPAN9
    nsv6916291copy number variation1nstd229human GRCh38 chr12: 3,215,072-3,215,182 , GRCh37.p13 chr12: 3,324,238-3,324,348 TSPAN9
    nsv6916072copy number variation1nstd229human GRCh38 chr12: 3,164,101-3,181,700 , GRCh37.p13 chr12: 3,273,267-3,290,866 TSPAN9
    nsv6915870copy number variation1nstd229human GRCh38 chr12: 2,822,991-3,101,779 , GRCh37.p13 chr12: 2,932,157-3,210,945 TSPAN9, TULP3, 8 more genes
    nsv6915755copy number variation1nstd229human GRCh38 chr12: 3,143,178-3,143,344 , GRCh37.p13 chr12: 3,252,344-3,252,510 TSPAN9
    nsv6914605copy number variation1nstd229human GRCh38 chr12: 3,125,642-3,217,387 , GRCh37.p13 chr12: 3,234,808-3,326,553 TSPAN9, RPS27P3
    nsv6914350copy number variation1nstd229human GRCh38 chr12: 3,188,138-3,247,016 , GRCh37.p13 chr12: 3,297,304-3,356,182 RPS27P3, TSPAN9
    nsv6914103copy number variation1nstd229human GRCh38 chr12: 3,198,101-3,218,300 , GRCh37.p13 chr12: 3,307,267-3,327,466 RPS27P3, TSPAN9
    nsv6913846copy number variation1nstd229human GRCh38 chr12: 3,093,114-3,093,446 , GRCh37.p13 chr12: 3,202,280-3,202,612 TSPAN9
    nsv6913695copy number variation1nstd229human GRCh38 chr12: 3,171,350-3,178,444 , GRCh37.p13 chr12: 3,280,516-3,287,610 TSPAN9
    nsv6912648copy number variation1nstd229human GRCh38 chr12: 3,085,601-3,119,000 , GRCh37.p13 chr12: 3,194,767-3,228,166 TSPAN9
    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