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 366

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5939850copy number variation1nstd209human GRCh38 chr15: 43,830,252-43,831,347 , GRCh37.p13 chr15: 44,122,450-44,123,545 WDR76
    nsv5935208copy number variation1nstd209human GRCh38 chr15: 43,849,719-43,850,476 , GRCh37.p13 chr15: 44,141,917-44,142,674 WDR76
    nsv5934395copy number variation1nstd209human GRCh38 chr15: 43,844,859-43,846,653 , GRCh37.p13 chr15: 44,137,057-44,138,851 WDR76
    nsv5852786copy number variation1nstd209human GRCh38 chr15: 43,830,221-43,831,370 , GRCh37.p13 chr15: 44,122,419-44,123,568 WDR76
    nsv5849963copy number variation1nstd209human GRCh38 chr15: 43,844,902-43,846,701 , GRCh37.p13 chr15: 44,137,100-44,138,899 WDR76
    nsv5590522copy number variation1nstd207human GRCh38 chr15: 43,844,859-43,846,653 , GRCh37.p13 chr15: 44,137,057-44,138,851 WDR76
    nsv5560302sequence alteration1nstd206human GRCh38 chr15: 43,825,989-43,826,520 , GRCh37.p13 chr15: 44,118,187-44,118,718 WDR76
    nsv5535209insertion1nstd206human GRCh38 chr15: 43,825,990-43,825,990 , GRCh37.p13 chr15: 44,118,188-44,118,188 WDR76
    nsv5513145copy number variation1nstd206human GRCh38 chr15: 43,844,862-43,846,654 , GRCh37.p13 chr15: 44,137,060-44,138,852 WDR76
    nsv5504320copy number variation1nstd206human GRCh38 chr15: 43,825,389-43,826,615 , GRCh37.p13 chr15: 44,117,587-44,118,813 WDR76
    nsv5498734copy number variation1nstd206human GRCh38 chr15: 43,830,255-43,831,348 , GRCh37.p13 chr15: 44,122,453-44,123,546 WDR76
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5357868translocation1nstd200human GRCh38 chr15: 43,831,348-43,831,348 , GRCh38 chr15: 43,830,255-43,830,255 , GRCh37.p13 chr15: 44,122,453-44,122,453 , GRCh37.p13 chr15: 44,123,546-44,123,546 WDR76
    nsv5343397translocation1nstd200human GRCh37 chr15: 44,123,545-44,123,545 , GRCh37 chr15: 44,122,453-44,122,453 , GRCh38.p12 chr15: 43,830,255-43,830,255 , GRCh38.p12 chr15: 43,831,347-43,831,347 WDR76
    nsv5340866translocation1nstd200human GRCh37 chr15: 44,118,718-44,118,718 , GRCh37 chr15: 44,118,197-44,118,197 , GRCh38.p12 chr15: 43,825,999-43,825,999 , GRCh38.p12 chr15: 43,826,520-43,826,520 WDR76
    nsv5323497translocation1nstd204human GRCh38.p13 chr15: 43,825,999-43,825,999 , GRCh38.p13 chr15: 43,826,520-43,826,520 , GRCh37.p13 chr15: 44,118,718-44,118,718 , GRCh37.p13 chr15: 44,118,197-44,118,197 WDR76
    nsv5318124copy number variation1nstd204human GRCh38.p13 chr15: 43,844,862-43,846,654 , GRCh37.p13 chr15: 44,137,060-44,138,852 WDR76
    nsv5274900copy number variation1nstd204human GRCh38.p13 chr15: 43,842,001-43,846,700 , GRCh37.p13 chr15: 44,134,199-44,138,898 WDR76
    nsv5271322copy number variation1nstd204human GRCh38.p13 chr15: 43,843,101-43,846,500 , GRCh37.p13 chr15: 44,135,299-44,138,698 WDR76
    nsv5267795copy number variation1nstd204human GRCh38.p13 chr15: 43,844,902-43,846,701 , GRCh37.p13 chr15: 44,137,100-44,138,899 WDR76
    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