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 942

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077031inversion1nstd229human GRCh38 chr11: 87,855,081-87,855,718 , GRCh37.p13 chr11: 87,565,973-87,566,610 LOC107984361, RAB38
    nsv7074300inversion1nstd229human GRCh38 chr11: 88,026,122-88,026,493 , GRCh37.p13 chr11: 87,759,290-87,759,661 RAB38
    nsv7073679inversion1nstd229human GRCh38 chr11: 88,085,487-88,094,151 , GRCh37.p13 chr11: 87,818,655-87,827,319 RAB38
    nsv7073461inversion1nstd229human GRCh38 chr11: 88,021,476-88,023,890 , GRCh37.p13 chr11: 87,754,644-87,757,058 RAB38
    nsv7073253inversion1nstd229human GRCh38 chr11: 88,160,921-88,179,681 , GRCh37.p13 chr11: 87,894,089-87,912,849 RAB38, MIR3166
    nsv7069436inversion1nstd229human GRCh38 chr11: 85,936,971-89,461,473 , GRCh37.p13 chr11: 85,648,014-89,194,641 , RNU6-1135P, 45 more genes
    nsv7066881inversion1nstd229human GRCh38 chr11: 87,893,282-87,916,839 , GRCh37.p13 chr11: 87,604,174-87,627,731 RAB38, LOC107984361
    nsv7066397inversion1nstd229human GRCh38 chr11: 88,080,569-88,087,376 , GRCh37.p13 chr11: 87,813,737-87,820,544 RAB38
    nsv7064092inversion1nstd229human GRCh38 chr11: 88,052,535-88,052,692 , GRCh37.p13 chr11: 87,785,703-87,785,860 RAB38
    nsv7063990inversion1nstd229human GRCh38 chr11: 88,154,736-88,179,674 , GRCh37.p13 chr11: 87,887,904-87,912,842 RAB38, MIR3166
    nsv7058586inversion1nstd229human GRCh38 chr11: 87,898,731-87,904,309 , GRCh37.p13 chr11: 87,609,623-87,615,201 LOC107984361, RAB38
    nsv6917863copy number variation1nstd229human GRCh38 chr11: 88,004,900-88,008,283 , GRCh37.p13 chr11: 87,738,379-87,741,451 RAB38
    nsv6917573copy number variation1nstd229human GRCh38 chr11: 88,086,158-88,164,916 , GRCh37.p13 chr11: 87,819,326-87,898,084 RAB38
    nsv6917542copy number variation1nstd229human GRCh38 chr11: 87,802,701-88,003,500 , GRCh37.p13 chr11: 87,513,593-87,688,378 RAB38, MTCYBP41, 1 more genes
    nsv6916866copy number variation1nstd229human GRCh38 chr11: 87,920,660-87,963,867 , GRCh37.p13 chr11: 87,631,552-87,674,759 RAB38
    nsv6916294copy number variation1nstd229human GRCh38 chr11: 87,966,933-87,967,142 , GRCh37.p13 chr11: 87,677,825-87,678,034 RAB38
    nsv6915815copy number variation1nstd229human GRCh38 chr11: 87,885,738-87,899,306 , GRCh37.p13 chr11: 87,596,630-87,610,198 LOC107984361, RAB38
    nsv6915021copy number variation1nstd229human GRCh38 chr11: 88,131,701-88,138,000 , GRCh37.p13 chr11: 87,864,869-87,871,168 RAB38
    nsv6914392copy number variation1nstd229human GRCh38 chr11: 87,818,064-87,818,173 , GRCh37.p13 chr11: 87,528,956-87,529,065 RAB38, LOC107984361
    nsv6914091copy number variation1nstd229human GRCh38 chr11: 87,944,209-87,951,692 , GRCh37.p13 chr11: 87,655,101-87,662,584 RAB38
    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