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 322

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112700copy number variation1nstd102humanPathogenic GRCh38 chr16: 46,385,317-61,223,349 , GRCh37.p13 chr16: 46,419,229-61,257,253 CPNE2, USB1, 275 more genes
    nsv5938106copy number variation1nstd209human GRCh38 chr16: 56,768,435-56,768,604 , GRCh37.p13 chr16: 56,802,347-56,802,516 NUP93
    nsv5932451copy number variation1nstd209human GRCh38 chr16: 56,809,924-56,809,996 , GRCh37.p13 chr16: 56,843,836-56,843,908 NUP93
    nsv5930591copy number variation1nstd209human GRCh38 chr16: 56,744,787-56,748,186 , GRCh37.p13 chr16: 56,778,699-56,782,098 NUP93
    nsv5870408copy number variation1nstd209human GRCh38 chr16: 56,744,764-56,748,163 , GRCh37.p13 chr16: 56,778,676-56,782,075 NUP93
    nsv5717640mobile element insertion1nstd211human GRCh38 chr16: 56,741,035-56,741,035 , GRCh37.p13 chr16: 56,774,947-56,774,947 NUP93
    nsv5662598insertion1nstd207human GRCh38 chr16: 56,808,153-56,808,153 , GRCh37.p13 chr16: 56,842,065-56,842,065 NUP93
    nsv5662232insertion1nstd207human GRCh38 chr16: 56,808,448-56,808,448 , GRCh37.p13 chr16: 56,842,360-56,842,360 NUP93
    nsv5661662insertion1nstd207human GRCh38 chr16: 56,808,356-56,808,356 , GRCh37.p13 chr16: 56,842,268-56,842,268 NUP93
    nsv5660000insertion1nstd207human GRCh38 chr16: 56,808,131-56,808,131 , GRCh37.p13 chr16: 56,842,043-56,842,043 NUP93
    nsv5655560insertion1nstd207human GRCh38 chr16: 56,739,517-56,739,517 , GRCh37.p13 chr16: 56,773,429-56,773,429 NUP93
    nsv5655445insertion1nstd207human GRCh38 chr16: 56,739,662-56,739,662 , GRCh37.p13 chr16: 56,773,574-56,773,574 NUP93
    nsv5655402insertion1nstd207human GRCh38 chr16: 56,740,127-56,740,127 , GRCh37.p13 chr16: 56,774,039-56,774,039 NUP93
    nsv5647068insertion1nstd207human GRCh38 chr16: 56,739,406-56,739,406 , GRCh37.p13 chr16: 56,773,318-56,773,318 NUP93
    nsv5645947insertion1nstd207human GRCh38 chr16: 56,739,342-56,739,342 , GRCh37.p13 chr16: 56,773,254-56,773,254 NUP93
    nsv5645894insertion1nstd207human GRCh38 chr16: 56,739,894-56,739,894 , GRCh37.p13 chr16: 56,773,806-56,773,806 NUP93
    nsv5591790copy number variation1nstd207human GRCh38 chr16: 56,808,450-56,808,558 , GRCh37.p13 chr16: 56,842,362-56,842,470 NUP93
    nsv5591107copy number variation1nstd207human GRCh38 chr16: 56,808,120-56,808,216 , GRCh37.p13 chr16: 56,842,032-56,842,128 NUP93
    nsv5589429copy number variation1nstd207human GRCh38 chr16: 56,739,578-56,739,950 , GRCh37.p13 chr16: 56,773,490-56,773,862 NUP93
    nsv5525454copy number variation1nstd206human GRCh38 chr16: 56,792,184-56,794,301 , GRCh37.p13 chr16: 56,826,096-56,828,213 NUP93
    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