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 565

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112685copy number variation1nstd102humannot provided GRCh37 chr1: 2,420,003-8,155,935 , GRCh38.p12 chr1: 2,488,564-8,095,875 LINC02780, C1orf174, 100 more genes
    nsv5883036copy number variation1nstd209human GRCh38 chr1: 3,480,889-3,481,073 , GRCh37.p13 chr1: 3,397,453-3,397,637 ARHGEF16
    nsv5612585insertion2nstd207human GRCh38 chr1: 3,475,042-3,475,042 , GRCh37.p13 chr1: 3,391,606-3,391,606 ARHGEF16
    nsv5609619insertion3nstd207human GRCh38 chr1: 3,477,303-3,477,303 , GRCh37.p13 chr1: 3,393,867-3,393,867 ARHGEF16
    nsv5606625insertion1nstd207human GRCh38 chr1: 3,475,352-3,475,352 , GRCh37.p13 chr1: 3,391,916-3,391,916 ARHGEF16
    nsv5583959copy number variation1nstd207human GRCh38 chr1: 3,475,052-3,475,171 , GRCh37.p13 chr1: 3,391,616-3,391,735 ARHGEF16
    nsv5577898copy number variation1nstd207human GRCh38 chr1: 3,470,863-3,470,914 , GRCh37.p13 chr1: 3,387,427-3,387,478 ARHGEF16
    nsv5377364translocation1nstd200human GRCh38 chr1: 33,361,231-33,361,231 , GRCh38 chr1: 3,465,183-3,465,183 , GRCh37.p13 chr1: 33,826,832-33,826,832 , GRCh37.p13 chr1: 3,381,747-3,381,747 PHC2, ARHGEF16, 1 more genes
    nsv5361388translocation1nstd200human GRCh38 chr1: 3,465,125-3,465,125 , GRCh38 chr1: 33,351,109-33,351,109 , GRCh37.p13 chr1: 3,381,689-3,381,689 , GRCh37.p13 chr1: 33,816,710-33,816,710 PHC2, ARHGEF16, 1 more genes
    nsv5339306translocation1nstd200human GRCh37 chr1: 33,816,710-33,816,710 , GRCh37 chr1: 3,381,689-3,381,689 , GRCh38.p12 chr1: 33,351,109-33,351,109 , GRCh38.p12 chr1: 3,465,125-3,465,125 PHC2, ARHGEF16, 1 more genes
    nsv5332497translocation1nstd200human GRCh37 chr1: 33,826,832-33,826,832 , GRCh37 chr1: 3,381,747-3,381,747 , GRCh38.p12 chr1: 3,465,183-3,465,183 , GRCh38.p12 chr1: 33,361,231-33,361,231 PHC2, ARHGEF16, 1 more genes
    nsv5281065copy number variation1nstd204human GRCh38.p13 chr1: 3,468,444-3,468,849 , GRCh37.p13 chr1: 3,385,008-3,385,413 ARHGEF16
    nsv5216584copy number variation1nstd204human GRCh38.p13 chr1: 3,475,101-3,475,400 , GRCh37.p13 chr1: 3,391,665-3,391,964 ARHGEF16
    nsv5209894copy number variation1nstd204human GRCh37.p13 chr1: 2,986,065-3,391,664 , GRCh38.p13 chr1: 3,069,501-3,475,100 ARHGEF16, PRDM16, 6 more genes
    nsv5208109copy number variation1nstd204human GRCh38.p13 chr1: 3,475,301-3,587,900 , GRCh37.p13 chr1: 3,391,865-3,504,464 MEGF6, MIR551A, 2 more genes
    nsv5205538copy number variation1nstd204human GRCh37.p13 chr1: 3,216,865-3,500,464 , GRCh38.p13 chr1: 3,300,301-3,583,900 MEGF6, ARHGEF16, 4 more genes
    nsv4894276copy number variation1nstd200human GRCh38 chr1: 2,989,984-4,291,637 , GRCh37.p13 chr1: 2,906,548-4,351,697 , LINC02780, 31 more genes
    nsv4782645copy number variation1nstd200human GRCh37 chr1: 3,387,299-3,387,400 , GRCh38.p12 chr1: 3,470,735-3,470,836 ARHGEF16
    nsv4755636insertion1nstd199human GRCh37 chr1: 3,393,797-3,393,797 , GRCh38.p12 chr1: 3,477,233-3,477,233 ARHGEF16
    nsv4743002copy number variation1nstd199human GRCh37 chr1: 3,391,475-3,391,594 , GRCh38.p12 chr1: 3,474,911-3,475,030 ARHGEF16
    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