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 268

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099244copy number variation1nstd231human GRCh38.p12 chr1: 166,864,890-169,028,321 , GRCh37 chr1: 166,834,127-168,997,559 CD247, DPT, 49 more genes
    nsv7095561copy number variation1nstd102humanUncertain significance GRCh37 chr1: 167,400,918-168,282,240 , GRCh38.p12 chr1: 167,431,681-168,313,002 GCSHP5, RNU6-1310P, 21 more genes
    nsv7039884inversion1nstd229human GRCh38 chr1: 159,817,036-167,858,499 , GRCh37.p13 chr1: 159,786,826-167,827,737 TRP-AGG2-1, FCGR2C, 228 more genes
    nsv6644244copy number variation1nstd229human GRCh38 chr1: 167,682,621-167,690,691 , GRCh37.p13 chr1: 167,651,858-167,659,928 RCSD1
    nsv6644239copy number variation1nstd229human GRCh38 chr1: 167,270,558-167,699,449 , GRCh37.p13 chr1: 167,239,795-167,668,686 POU2F1, LOC101928512, 6 more genes
    nsv6644189copy number variation1nstd229human GRCh38 chr1: 167,693,872-167,693,925 , GRCh37.p13 chr1: 167,663,109-167,663,162 RCSD1
    nsv6643759copy number variation1nstd229human GRCh38 chr1: 167,698,256-167,703,331 , GRCh37.p13 chr1: 167,667,493-167,672,568 RCSD1
    nsv6643758copy number variation1nstd229human GRCh38 chr1: 167,666,219-167,666,640 , GRCh37.p13 chr1: 167,635,456-167,635,877 RCSD1
    nsv6643757copy number variation1nstd229human GRCh38 chr1: 167,659,105-167,685,137 , GRCh37.p13 chr1: 167,628,342-167,654,374 RCSD1
    nsv6643756copy number variation1nstd229human GRCh38 chr1: 167,632,344-167,636,015 , GRCh37.p13 chr1: 167,601,581-167,605,252 RCSD1
    nsv6544966inversion1nstd223human GRCh38 chr1: 167,665,053-167,665,750 , GRCh37.p13 chr1: 167,634,290-167,634,987 RCSD1
    nsv6540250inversion1nstd223human GRCh38 chr1: 163,441,141-169,028,378 , GRCh37.p13 chr1: 163,410,931-168,997,616 LOC107985452, NMNAT1P2, 96 more genes
    nsv6325883copy number variation1nstd223human GRCh38 chr1: 167,655,095-167,655,616 , GRCh37.p13 chr1: 167,624,332-167,624,853 RCSD1
    nsv6320092copy number variation1nstd223human GRCh38 chr1: 167,693,872-167,693,925 , GRCh37.p13 chr1: 167,663,109-167,663,162 RCSD1
    nsv6319607copy number variation1nstd223human GRCh38 chr1: 167,702,001-167,704,280 , GRCh37.p13 chr1: 167,671,238-167,673,517 RCSD1
    nsv6313719copy number variation1nstd102humanPathogenic GRCh37 chr1: 162,330,810-171,532,331 , GRCh38.p12 chr1: 162,361,020-171,563,192 LOC100420658, LOC105371610, 167 more genes
    nsv6313602copy number variation1nstd102humanPathogenic GRCh37 chr1: 167,391,422-171,843,613 , GRCh38.p12 chr1: 167,422,185-171,874,473 DCAF6, SELE, 101 more genes
    nsv6295714copy number variation1nstd186human GRCh37 chr1: 167,663,110-167,663,162 , GRCh38.p12 chr1: 167,693,873-167,693,925 RCSD1
    nsv6293271mobile element insertion1nstd186human GRCh37 chr1: 167,618,739-167,618,790 , GRCh38.p12 chr1: 167,649,502-167,649,553 RCSD1
    nsv6245570mobile element insertion1nstd215human GRCh38 chr1: 167,682,707-167,682,707 , GRCh37.p13 chr1: 167,651,944-167,651,944 RCSD1
    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