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 387

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6123443copy number variation1nstd186human GRCh37 chr20: 35,732,881-35,734,450 , GRCh38.p12 chr20: 37,104,478-37,106,047 MROH8
    nsv5976704inversion1nstd209human GRCh38 chr20: 36,955,252-45,585,469 , GRCh37.p13 chr20: 35,583,655-44,214,108 , ADA, 180 more genes
    nsv5958550copy number variation1nstd209human GRCh38 chr20: 37,125,228-37,125,870 , GRCh37.p13 chr20: 35,753,631-35,754,273 MROH8
    nsv5887380copy number variation2nstd209human GRCh38 chr20: 37,103,892-37,107,212 , GRCh37.p13 chr20: 35,732,295-35,735,615 MROH8
    nsv5887210copy number variation1nstd209human GRCh38 chr20: 37,140,629-37,153,443 , GRCh37.p13 chr20: 35,769,032-35,781,846 MROH8
    nsv5709774mobile element insertion2nstd211human GRCh38 chr20: 37,127,628-37,127,628 , GRCh37.p13 chr20: 35,756,031-35,756,031 MROH8
    nsv5705752mobile element insertion1nstd211human GRCh38 chr20: 37,108,329-37,108,329 , GRCh37.p13 chr20: 35,736,732-35,736,732 MROH8
    nsv5664755insertion1nstd207human GRCh38 chr20: 37,104,533-37,104,533 , GRCh37.p13 chr20: 35,732,936-35,732,936 MROH8
    nsv5539701insertion1nstd206human GRCh38 chr20: 37,104,444-37,104,480 , GRCh37.p13 chr20: 35,732,847-35,732,883 MROH8
    nsv5536384insertion1nstd206human GRCh38 chr20: 37,157,204-37,157,244 , GRCh37.p13 chr20: 35,785,607-35,785,647 MROH8
    nsv5532192copy number variation1nstd206human GRCh38 chr20: 37,104,445-37,106,090 , GRCh37.p13 chr20: 35,732,848-35,734,493 MROH8
    nsv5527701copy number variation1nstd206human GRCh38 chr20: 37,049,169-37,196,727 , GRCh37.p13 chr20: 35,677,572-35,825,130 RPN2, RPS27AP3, 3 more genes
    nsv5524479copy number variation1nstd206human GRCh38 chr20: 37,140,825-37,144,465 , GRCh37.p13 chr20: 35,769,228-35,772,868 MROH8
    nsv5520614copy number variation1nstd206human GRCh38 chr20: 37,125,228-37,125,904 , GRCh37.p13 chr20: 35,753,631-35,754,307 MROH8
    nsv5520493copy number variation1nstd206human GRCh38 chr20: 37,127,410-37,127,628 , GRCh37.p13 chr20: 35,755,813-35,756,031 MROH8
    nsv5518550copy number variation1nstd206human GRCh38 chr20: 37,123,129-37,124,714 , GRCh37.p13 chr20: 35,751,532-35,753,117 MROH8
    nsv5426764mobile element insertion1nstd206human GRCh38 chr20: 37,108,329-37,108,380 , GRCh37.p13 chr20: 35,736,732-35,736,783 MROH8
    nsv5392832copy number variation1nstd186human GRCh37 chr20: 35,732,880-35,734,455 , GRCh38.p12 chr20: 37,104,477-37,106,052 MROH8
    nsv5391167copy number variation1nstd186human GRCh37 chr20: 35,732,881-35,734,455 , GRCh38.p12 chr20: 37,104,478-37,106,052 MROH8
    nsv5350316translocation1nstd200human GRCh38 chr20: 37,125,904-37,125,904 , GRCh38 chr20: 37,125,228-37,125,228 , GRCh37.p13 chr20: 35,753,631-35,753,631 , GRCh37.p13 chr20: 35,754,307-35,754,307 MROH8
    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