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 298

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5959411insertion1nstd209human GRCh38 chr2: 237,828,868-237,828,868 , GRCh37.p13 chr2: 238,737,511-238,737,511 RBM44
    nsv5897290copy number variation1nstd209human GRCh38 chr2: 237,829,911-237,831,930 , GRCh37.p13 chr2: 238,738,554-238,740,573 RBM44
    nsv5887748copy number variation1nstd209human GRCh38 chr2: 237,837,657-237,838,019 , GRCh37.p13 chr2: 238,746,300-238,746,662 RBM44
    nsv5832573copy number variation1nstd209human GRCh38 chr2: 237,829,861-237,831,699 , GRCh37.p13 chr2: 238,738,504-238,740,342 RBM44
    nsv5689797mobile element insertion1nstd211human GRCh38 chr2: 237,804,624-237,804,624 , GRCh37.p13 chr2: 238,713,267-238,713,267 RBM44
    nsv5684720mobile element insertion2nstd211human GRCh38 chr2: 237,828,883-237,828,883 , GRCh37.p13 chr2: 238,737,526-238,737,526 RBM44
    nsv5676292mobile element insertion1nstd211human GRCh38 chr2: 237,804,607-237,804,607 , GRCh37.p13 chr2: 238,713,250-238,713,250 RBM44
    nsv5616606insertion1nstd207human GRCh38 chr2: 237,828,868-237,828,868 , GRCh37.p13 chr2: 238,737,511-238,737,511 RBM44
    nsv5565025copy number variation1nstd207human GRCh38 chr2: 237,837,657-237,838,019 , GRCh37.p13 chr2: 238,746,300-238,746,662 RBM44
    nsv5537648insertion1nstd206human GRCh38 chr2: 237,828,883-237,828,917 , GRCh37.p13 chr2: 238,737,526-238,737,560 RBM44
    nsv5447132copy number variation1nstd206human GRCh38 chr2: 237,837,657-237,838,049 , GRCh37.p13 chr2: 238,746,300-238,746,692 RBM44
    nsv5444800copy number variation1nstd206human GRCh38 chr2: 237,829,913-237,831,931 , GRCh37.p13 chr2: 238,738,556-238,740,574 RBM44
    nsv5443950copy number variation1nstd206human GRCh38 chr2: 237,803,795-237,843,033 , GRCh37.p13 chr2: 238,712,438-238,751,676 RBM44
    nsv5434787copy number variation1nstd206human GRCh38 chr2: 237,836,898-237,867,029 , GRCh37.p13 chr2: 238,745,541-238,775,672 RBM44, RAMP1
    nsv5401960mobile element insertion1nstd206human GRCh38 chr2: 237,804,624-237,804,658 , GRCh37.p13 chr2: 238,713,267-238,713,301 RBM44
    nsv5381323copy number variation1nstd102humanPathogenic GRCh37 chr2: 237,201,756-243,048,760 , GRCh38.p12 chr2: 236,293,113-242,106,609 LRRFIP1, GPR35, 133 more genes
    nsv5311419copy number variation1nstd204human GRCh38.p13 chr2: 237,837,657-237,838,049 , GRCh37.p13 chr2: 238,746,300-238,746,692 RBM44
    nsv5219681copy number variation1nstd204human GRCh38.p13 chr2: 237,837,701-237,838,000 , GRCh37.p13 chr2: 238,746,344-238,746,643 RBM44
    nsv5072137mobile element insertion1nstd203human GRCh38 chr2: 237,828,883-237,828,883 , GRCh37.p13 chr2: 238,737,526-238,737,526 RBM44
    nsv5071990mobile element insertion1nstd203human GRCh38 chr2: 237,828,867-237,828,883 , GRCh37.p13 chr2: 238,737,510-238,737,526 RBM44
    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