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 733

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5968598inversion1nstd209human GRCh38 chr1: 85,537,470-85,544,006 , GRCh37.p13 chr1: 86,003,153-86,009,689 DDAH1
    nsv5885982copy number variation1nstd209human GRCh38 chr1: 85,440,802-85,440,875 , GRCh37.p13 chr1: 85,906,485-85,906,558 DDAH1
    nsv5880765copy number variation1nstd209human GRCh38 chr1: 85,471,192-85,473,683 , GRCh37.p13 chr1: 85,936,875-85,939,366 DDAH1
    nsv5876509copy number variation1nstd209human GRCh38 chr1: 85,536,629-85,538,956 , GRCh37.p13 chr1: 86,002,312-86,004,639 DDAH1
    nsv5872636copy number variation1nstd209human GRCh38 chr1: 85,359,314-85,359,392 , GRCh37.p13 chr1: 85,824,997-85,825,075 DDAH1
    nsv5871987copy number variation1nstd209human GRCh38 chr1: 85,445,302-85,449,718 , GRCh37.p13 chr1: 85,910,985-85,915,401 DDAH1
    nsv5870700copy number variation1nstd209human GRCh38 chr1: 85,464,397-85,464,609 , GRCh37.p13 chr1: 85,930,080-85,930,292 DDAH1
    nsv5830513copy number variation1nstd209human GRCh38 chr1: 85,537,611-85,543,660 , GRCh37.p13 chr1: 86,003,294-86,009,343 DDAH1
    nsv5830512copy number variation1nstd209human GRCh38 chr1: 85,537,561-85,538,903 , GRCh37.p13 chr1: 86,003,244-86,004,586 DDAH1
    nsv5830511copy number variation1nstd209human GRCh38 chr1: 85,525,252-85,528,451 , GRCh37.p13 chr1: 85,990,935-85,994,134 DDAH1
    nsv5830496copy number variation1nstd209human GRCh38 chr1: 85,471,125-85,473,649 , GRCh37.p13 chr1: 85,936,808-85,939,332 DDAH1
    nsv5830495copy number variation1nstd209human GRCh38 chr1: 85,445,260-85,449,711 , GRCh37.p13 chr1: 85,910,943-85,915,394 DDAH1
    nsv5723330mobile element insertion1nstd211human GRCh38 chr1: 85,376,181-85,376,181 , GRCh37.p13 chr1: 85,841,864-85,841,864 DDAH1
    nsv5681812mobile element insertion1nstd211human GRCh38 chr1: 85,500,143-85,500,143 , GRCh37.p13 chr1: 85,965,826-85,965,826 DDAH1
    nsv5681230mobile element insertion2nstd211human GRCh38 chr1: 85,559,117-85,559,117 , GRCh37.p13 chr1: 86,024,800-86,024,800 DDAH1
    nsv5679873mobile element insertion2nstd211human GRCh38 chr1: 85,577,597-85,577,597 , GRCh37.p13 chr1: 86,043,280-86,043,280 DDAH1
    nsv5675733mobile element insertion1nstd211human GRCh38 chr1: 85,380,260-85,380,260 , GRCh37.p13 chr1: 85,845,943-85,845,943 DDAH1
    nsv5614310insertion1nstd207human GRCh38 chr1: 85,536,977-85,536,977 , GRCh37.p13 chr1: 86,002,660-86,002,660 DDAH1
    nsv5609948insertion1nstd207human GRCh38 chr1: 85,518,093-85,518,093 , GRCh37.p13 chr1: 85,983,776-85,983,776 DDAH1
    nsv5607887insertion1nstd207human GRCh38 chr1: 85,517,805-85,517,805 , GRCh37.p13 chr1: 85,983,488-85,983,488 DDAH1
    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