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 553

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5963315insertion1nstd209human GRCh38 chr2: 241,812,487-241,812,487 , GRCh37.p13 chr2: 242,753,582-242,753,582 NEU4
    nsv5905088copy number variation1nstd209human GRCh38 chr2: 241,809,029-241,809,105 , GRCh37.p13 chr2: 242,750,124-242,750,200 NEU4
    nsv5903630copy number variation1nstd209human GRCh38 chr2: 241,812,560-241,812,636 , GRCh37.p13 chr2: 242,753,698-242,753,774 NEU4
    nsv5898069copy number variation1nstd209human GRCh38 chr2: 241,805,301-241,807,768 , GRCh37.p13 chr2: 242,746,336-242,748,856 NEU4
    nsv5896830copy number variation1nstd209human GRCh38 chr2: 241,805,296-241,807,881 , GRCh37.p13 chr2: 242,746,331-242,748,972 NEU4
    nsv5895028copy number variation1nstd209human GRCh38 chr2: 241,805,290-241,808,011 , GRCh37.p13 chr2: 242,746,325-242,749,094 NEU4
    nsv5888770copy number variation1nstd209human GRCh38 chr2: 241,805,397-241,807,688 , GRCh37.p13 chr2: 242,746,430-242,748,776 NEU4
    nsv5832909copy number variation1nstd209human GRCh38 chr2: 241,808,036-241,819,054 , GRCh37.p13 chr2: 242,749,119-242,760,382 LOC107986004, NEU4
    nsv5832272copy number variation2nstd209human GRCh38 chr2: 241,816,155-241,817,254 , GRCh37.p13 chr2: 242,757,481-242,758,580 LOC107986004, NEU4
    nsv5621836insertion1nstd207human GRCh38 chr2: 241,810,758-241,810,758 , GRCh37.p13 chr2: 242,751,853-242,751,853 NEU4
    nsv5620467insertion2nstd207human GRCh38 chr2: 241,812,487-241,812,487 , GRCh37.p13 chr2: 242,753,582-242,753,582 NEU4
    nsv5615696insertion2nstd207human GRCh38 chr2: 241,813,819-241,813,819 , GRCh37.p13 chr2: 242,754,957-242,754,957 NEU4
    nsv5614407insertion1nstd207human GRCh38 chr2: 241,807,607-241,807,607 , GRCh37.p8 chr: NaN-NaN , GRCh37.p13 chr: NaN-NaN NEU4
    nsv5613505insertion1nstd207human GRCh38 chr2: 241,808,012-241,808,012 , GRCh37.p13 chr2: 242,749,095-242,749,095 NEU4
    nsv5609886insertion1nstd207human GRCh38 chr2: 241,809,074-241,809,074 , GRCh37.p13 chr2: 242,750,169-242,750,169 NEU4
    nsv5607174insertion1nstd207human GRCh38 chr2: 241,807,888-241,807,888 , GRCh37.p8 chr: NaN-NaN , GRCh37.p13 chr: NaN-NaN NEU4
    nsv5605714insertion1nstd207human GRCh38 chr2: 241,808,040-241,808,040 , GRCh37.p13 chr2: 242,749,123-242,749,123 NEU4
    nsv5604729insertion1nstd207human GRCh38 chr2: 241,815,394-241,815,394 , GRCh37.p13 chr2: 242,756,591-242,756,591 NEU4
    nsv5578540copy number variation1nstd207human GRCh38 chr2: 241,807,338-241,807,411 , GRCh37.p13 chr2: 242,748,430-242,748,502 NEU4
    nsv5575555copy number variation1nstd207human GRCh38 chr2: 241,806,535-241,807,411 , GRCh37.p13 chr2: 242,747,608-242,748,502 NEU4
    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