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 450

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5979328inversion1nstd209human GRCh38 chr19: 32,019,307-33,218,671 , GRCh37.p13 chr19: 32,510,213-33,709,577 , LRP3, 28 more genes
    nsv5974064insertion1nstd209human GRCh38 chr19: 32,954,827-32,954,827 , GRCh37.p13 chr19: 33,445,733-33,445,733 CEP89
    nsv5946452copy number variation1nstd209human GRCh38 chr19: 32,920,079-32,920,765 , GRCh37.p13 chr19: 33,410,985-33,411,671 CEP89
    nsv5941724copy number variation1nstd209human GRCh38 chr19: 32,938,811-32,939,538 , GRCh37.p13 chr19: 33,429,717-33,430,444 CEP89
    nsv5714403mobile element insertion1nstd211human GRCh38 chr19: 32,926,084-32,926,084 , GRCh37.p13 chr19: 33,416,990-33,416,990 CEP89
    nsv5713637mobile element insertion2nstd211human GRCh38 chr19: 32,942,596-32,942,596 , GRCh37.p13 chr19: 33,433,502-33,433,502 CEP89
    nsv5653962insertion1nstd207human GRCh38 chr19: 32,954,827-32,954,827 , GRCh37.p13 chr19: 33,445,733-33,445,733 CEP89
    nsv5555405inversion1nstd206human GRCh38 chr19: 32,878,140-32,959,661 , GRCh37.p13 chr19: 33,369,046-33,450,567 CEP89
    nsv5522732copy number variation1nstd206human GRCh38 chr19: 32,924,695-32,924,824 , GRCh37.p13 chr19: 33,415,601-33,415,730 CEP89
    nsv5522329copy number variation1nstd206human GRCh38 chr19: 32,901,133-32,907,726 , GRCh37.p13 chr19: 33,392,039-33,398,632 CEP89
    nsv5519571copy number variation1nstd206human GRCh38 chr19: 32,938,787-32,939,582 , GRCh37.p13 chr19: 33,429,693-33,430,488 CEP89
    nsv5518403copy number variation1nstd206human GRCh38 chr19: 32,969,722-32,969,781 , GRCh37.p13 chr19: 33,460,628-33,460,687 CEP89
    nsv5515543copy number variation1nstd206human GRCh38 chr19: 32,941,416-32,942,261 , GRCh37.p13 chr19: 33,432,322-33,433,167 CEP89
    nsv5417606mobile element insertion1nstd206human GRCh38 chr19: 32,942,596-32,942,647 , GRCh37.p13 chr19: 33,433,502-33,433,553 CEP89
    nsv5359723translocation1nstd200human GRCh38 chr19: 32,941,416-32,941,416 , GRCh38 chr19: 32,942,261-32,942,261 , GRCh37.p13 chr19: 33,432,322-33,432,322 , GRCh37.p13 chr19: 33,433,167-33,433,167 CEP89
    nsv5343261translocation1nstd200human GRCh37 chr20: 26,220,634-26,220,634 , GRCh37 chr19: 33,444,264-33,444,264 , GRCh38.p12 chr19: 32,953,358-32,953,358 , GRCh38.p12 chr20: 26,239,998-26,239,998 CEP89
    nsv5342245translocation1nstd200human GRCh37 chr19: 33,463,022-33,463,022 , GRCh37 chr19: 33,462,664-33,462,664 , GRCh38.p12 chr19: 32,971,758-32,971,758 , GRCh38.p12 chr19: 32,972,116-32,972,116 FAAP24, CEP89
    nsv5332147translocation1nstd200human GRCh37 chr19: 33,444,266-33,444,266 , GRCh37 chr3: 75,983,387-75,983,387 , GRCh38.p12 chr3: 75,934,236-75,934,236 , GRCh38.p12 chr19: 32,953,360-32,953,360 ROBO2, CEP89
    nsv5323117copy number variation1nstd204human GRCh38.p13 chr19: 32,920,921-32,921,230 , GRCh37.p13 chr19: 33,411,827-33,412,136 CEP89
    nsv5297561copy number variation1nstd204human GRCh38.p13 chr19: 32,938,149-32,940,898 , GRCh37.p13 chr19: 33,429,055-33,431,804 CEP89
    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