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 707

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145421copy number variation1nstd232human GRCh37.p13 chr11: 3,916,927-3,916,976 , GRCh38.p12 chr11: 3,895,697-3,895,746 STIM1
    nsv7140909copy number variation1nstd232human GRCh37.p13 chr11: 3,916,908-3,916,968 , GRCh38.p12 chr11: 3,895,678-3,895,738 STIM1
    nsv7094186copy number variation1nstd102humanUncertain significance GRCh37 chr11: 721,044-3,988,932 , GRCh38.p12 chr11: 721,044-3,967,702 OR7E117P, RPLP2, 124 more genes
    nsv7094168copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 4,045,083-4,045,237 , GRCh38.p12 chr11: 4,023,853-4,024,007 STIM1
    nsv7093688copy number variation1nstd102humanUncertain significance GRCh37 chr11: 4,112,492-4,113,028 , GRCh38.p12 chr11: 4,091,262-4,091,798 STIM1
    nsv7060920inversion1nstd229human GRCh38 chr11: 4,014,616-4,536,086 , GRCh37.p13 chr11: 4,035,846-4,557,316 RDXP1, RRM1, 19 more genes
    nsv6917011copy number variation1nstd229human GRCh38 chr11: 2,693,282-9,207,515 , GRCh37.p13 chr11: 2,714,512-9,229,062 LOC105376526, OR51E2, 279 more genes
    nsv6916547copy number variation1nstd229human GRCh38 chr11: 3,861,935-3,867,489 , GRCh37.p13 chr11: 3,883,165-3,888,719 STIM1
    nsv6916129copy number variation1nstd229human GRCh38 chr11: 3,833,721-4,728,036 , GRCh37.p13 chr11: 3,854,951-4,749,266 OR52K1, OR52B4, 39 more genes
    nsv6915681copy number variation1nstd229human GRCh38 chr11: 3,912,422-3,935,161 , GRCh37.p13 chr11: 3,933,652-3,956,391 STIM1
    nsv6914308copy number variation1nstd229human GRCh38 chr11: 4,061,101-4,065,700 , GRCh37.p13 chr11: 4,082,331-4,086,930 STIM1
    nsv6914177copy number variation1nstd229human GRCh38 chr11: 4,060,165-4,060,642 , GRCh37.p13 chr11: 4,081,395-4,081,872 STIM1
    nsv6911567copy number variation1nstd229human GRCh38 chr11: 3,864,308-3,870,082 , GRCh37.p13 chr11: 3,885,538-3,891,312 STIM1
    nsv6909618copy number variation1nstd229human GRCh38 chr11: 3,884,099-3,891,684 , GRCh37.p13 chr11: 3,905,329-3,912,914 PPIAP40, STIM1
    nsv6908918copy number variation1nstd229human GRCh38 chr11: 3,866,401-3,871,000 , GRCh37.p13 chr11: 3,887,631-3,892,230 STIM1
    nsv6908799copy number variation1nstd229human GRCh38 chr11: 3,872,107-3,872,468 , GRCh37.p13 chr11: 3,893,337-3,893,698 STIM1
    nsv6908492copy number variation1nstd229human GRCh38 chr11: 3,921,625-3,921,778 , GRCh37.p13 chr11: 3,942,855-3,943,008 STIM1
    nsv6907378copy number variation1nstd229human GRCh38 chr11: 3,869,182-3,872,898 , GRCh37.p13 chr11: 3,890,412-3,894,128 STIM1
    nsv6907196copy number variation1nstd229human GRCh38 chr11: 3,997,342-4,011,996 , GRCh37.p13 chr11: 4,018,572-4,033,226 STIM1
    nsv6906464copy number variation1nstd229human GRCh38 chr11: 4,065,727-4,066,290 , GRCh37.p13 chr11: 4,086,957-4,087,520 STIM1
    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