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 265

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7070560inversion1nstd229human GRCh38 chr10: 22,991,362-22,991,409 , GRCh37.p13 chr10: 23,280,291-23,280,338 ARMC3
    nsv6896365copy number variation1nstd229human GRCh38 chr10: 23,001,491-23,004,158 , GRCh37.p13 chr10: 23,290,420-23,293,087 LOC107984215, ARMC3
    nsv6892043copy number variation1nstd229human GRCh38 chr10: 22,946,101-22,986,700 , GRCh37.p13 chr10: 23,235,030-23,275,629 ARMC3
    nsv6891933copy number variation1nstd229human GRCh38 chr10: 22,933,144-22,959,875 , GRCh37.p13 chr10: 23,222,073-23,248,804 ARMC3
    nsv6885076copy number variation1nstd229human GRCh38 chr10: 22,929,266-22,929,293 , GRCh37.p13 chr10: 23,218,195-23,218,222 ARMC3
    nsv6885070copy number variation1nstd229human GRCh38 chr10: 23,024,081-23,024,795 , GRCh37.p13 chr10: 23,313,010-23,313,724 LOC107984215, ARMC3
    nsv6885032copy number variation1nstd229human GRCh38 chr10: 22,990,915-23,000,178 , GRCh37.p13 chr10: 23,279,844-23,289,107 LOC107984215, ARMC3, 1 more genes
    nsv6883207copy number variation1nstd229human GRCh38 chr10: 22,931,201-22,951,623 , GRCh37.p13 chr10: 23,220,130-23,240,552 ARMC3
    nsv6882739copy number variation1nstd229human GRCh38 chr10: 22,932,592-22,934,680 , GRCh37.p13 chr10: 23,221,521-23,223,609 ARMC3
    nsv6878708copy number variation1nstd229human GRCh38 chr10: 22,925,801-22,931,400 , GRCh37.p13 chr10: 23,214,730-23,220,329 ARMC3
    nsv6638019copy number variation1nstd102humanUncertain significance GRCh37 chr10: 22,208,767-23,220,277 , GRCh38.p12 chr10: 21,919,838-22,931,348 ADIPOR1P1, LINC03027, 19 more genes
    nsv6589795inversion1nstd223human GRCh38 chr10: 23,017,488-23,018,811 , GRCh37.p13 chr10: 23,306,417-23,307,740 LOC107984215, ARMC3
    nsv6589216inversion1nstd223human GRCh38 chr10: 22,952,264-22,952,444 , GRCh37.p13 chr10: 23,241,193-23,241,373 ARMC3
    nsv6587674inversion1nstd223human GRCh38 chr10: 22,963,667-22,964,684 , GRCh37.p13 chr10: 23,252,596-23,253,613 ARMC3
    nsv6583098inversion1nstd223human GRCh38 chr10: 22,928,946-22,929,664 , GRCh37.p13 chr10: 23,217,875-23,218,593 ARMC3
    nsv6446577copy number variation1nstd223human GRCh38 chr10: 22,981,363-22,982,142 , GRCh37.p13 chr10: 23,270,292-23,271,071 ARMC3
    nsv6444072copy number variation1nstd223human GRCh38 chr10: 23,025,601-23,026,600 , GRCh37.p13 chr10: 23,314,530-23,315,529 ARMC3, LOC107984215
    nsv6436047copy number variation1nstd223human GRCh38 chr10: 22,925,801-22,931,400 , GRCh37.p13 chr10: 23,214,730-23,220,329 ARMC3
    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