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 292

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057970inversion1nstd229human GRCh38 chr5: 39,369,727-42,623,585 , GRCh37.p13 chr5: 39,369,829-42,623,687 LINC02996, DAB2, 36 more genes
    nsv7051859inversion1nstd229human GRCh38 chr5: 41,806,643-42,640,726 , GRCh37.p13 chr5: 41,806,745-42,640,828 RPS2P22, SERBP1P6, 11 more genes
    nsv7041157inversion1nstd229human GRCh38 chr5: 40,200,630-42,327,400 , GRCh37.p13 chr5: 40,200,732-42,327,502 RNU7-161P, LINC02996, 26 more genes
    nsv6775848copy number variation1nstd229human GRCh38 chr5: 42,020,614-42,059,433 , GRCh37.p13 chr5: 42,020,716-42,059,535 FBXO4
    nsv6775745copy number variation1nstd229human GRCh38 chr5: 41,957,007-41,973,447 , GRCh37.p13 chr5: 41,957,109-41,973,549 MTHFD2P6, FBXO4
    nsv6775664copy number variation1nstd229human GRCh38 chr5: 41,972,317-42,019,714 , GRCh37.p13 chr5: 41,972,419-42,019,816 FBXO4
    nsv6772752copy number variation1nstd229human GRCh38 chr5: 41,871,542-42,048,800 , GRCh37.p13 chr5: 41,871,644-42,048,902 RPS2P22, LOC102723752, 6 more genes
    nsv6772408copy number variation1nstd229human GRCh38 chr5: 41,998,996-42,003,298 , GRCh37.p13 chr5: 41,999,098-42,003,400 FBXO4
    nsv6772346copy number variation1nstd229human GRCh38 chr5: 41,944,113-41,956,148 , GRCh37.p13 chr5: 41,944,215-41,956,250 RPSAP38, FBXO4
    nsv6771615copy number variation1nstd229human GRCh38 chr5: 41,879,700-42,913,283 , GRCh37.p13 chr5: 41,879,802-42,913,385 LOC100419715, PRELID3BP5, 14 more genes
    nsv6770863copy number variation1nstd229human GRCh38 chr5: 41,919,781-42,487,753 , GRCh37.p13 chr5: 41,919,883-42,487,855 RIMOC1, FBXO4, 7 more genes
    nsv6770393copy number variation1nstd229human GRCh38 chr5: 42,000,301-42,002,800 , GRCh37.p13 chr5: 42,000,403-42,002,902 FBXO4
    nsv6770010copy number variation1nstd229human GRCh38 chr5: 41,960,937-41,961,004 , GRCh37.p13 chr5: 41,961,039-41,961,106 FBXO4
    nsv6769814copy number variation1nstd229human GRCh38 chr5: 39,447,462-42,528,554 , GRCh37.p13 chr5: 39,447,564-42,528,656 RNU7-161P, OXCT1, 35 more genes
    nsv6769807copy number variation1nstd229human GRCh38 chr5: 41,937,419-41,941,771 , GRCh37.p13 chr5: 41,937,521-41,941,873 FBXO4
    nsv6768225copy number variation1nstd229human GRCh38 chr5: 41,950,270-41,951,224 , GRCh37.p13 chr5: 41,950,372-41,951,326 FBXO4, RPSAP38
    nsv6767293copy number variation1nstd229human GRCh38 chr5: 42,012,456-42,016,551 , GRCh37.p13 chr5: 42,012,558-42,016,653 FBXO4
    nsv6766023copy number variation1nstd229human GRCh38 chr5: 41,937,301-41,941,600 , GRCh37.p13 chr5: 41,937,403-41,941,702 FBXO4
    nsv6765545copy number variation1nstd229human GRCh38 chr5: 41,946,080-41,950,246 , GRCh37.p13 chr5: 41,946,182-41,950,348 RPSAP38, FBXO4
    nsv6765401copy number variation1nstd229human GRCh38 chr5: 42,034,778-42,039,815 , GRCh37.p13 chr5: 42,034,880-42,039,917 FBXO4
    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