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 179

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094547copy number variation1nstd102humanPathogenic GRCh37 chr15: 62,146,656-64,747,263 , GRCh38.p12 chr15: 61,854,457-64,455,064 C2CD4A, SNX22, 40 more genes
    nsv7071327inversion1nstd229human GRCh38 chr15: 55,806,321-63,352,065 , GRCh37.p13 chr15: 56,098,519-63,644,264 LOC107984805, TPM1-AS, 120 more genes
    nsv7061583inversion1nstd229human GRCh38 chr15: 63,157,752-63,157,776 , GRCh37.p13 chr15: 63,449,951-63,449,975 RPS27L
    nsv6977284copy number variation1nstd229human GRCh38 chr15: 63,155,001-63,163,000 , GRCh37.p13 chr15: 63,447,200-63,455,199 RPS27L
    nsv6969710copy number variation1nstd229human GRCh38 chr15: 63,156,457-63,160,145 , GRCh37.p13 chr15: 63,448,656-63,452,344 RPS27L
    nsv6968256copy number variation1nstd229human GRCh38 chr15: 63,149,543-63,149,620 , GRCh37.p13 chr15: 63,441,742-63,441,819 RPS27L
    nsv6960684copy number variation1nstd229human GRCh38 chr15: 62,287,754-63,705,691 , GRCh37.p13 chr15: 62,579,953-63,997,890 MIR8067, RPS27L, 21 more genes
    nsv6637384copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,589,845-63,543,438 , GRCh38.p12 chr15: 48,297,648-63,251,239 LINC03065, FAM227B, 228 more genes
    nsv6593180inversion1nstd223human GRCh38 chr15: 63,148,880-63,149,525 , GRCh37.p13 chr15: 63,441,079-63,441,724 RPS27L
    nsv6504211copy number variation1nstd223human GRCh38 chr15: 63,148,909-63,150,665 , GRCh37.p13 chr15: 63,441,108-63,442,864 RPS27L
    nsv6270702copy number variation1nstd214human GRCh38 chr15: 63,149,543-63,149,619 , GRCh37.p13 chr15: 63,441,742-63,441,818 RPS27L
    nsv6235282insertion1nstd214human GRCh38 chr15: 63,146,250-63,146,250 , GRCh37.p13 chr15: 63,438,449-63,438,449 RPS27L
    nsv6133150copy number variation1nstd213human GRCh37 chr15: 59,870,000-66,270,001 , GRCh38.p12 chr15: 59,577,801-65,977,663 GTF2A2, OAZ2, 115 more genes
    nsv6131043insertion1nstd186human GRCh37 chr15: 63,438,480-63,438,500 , GRCh38.p12 chr15: 63,146,281-63,146,301 RPS27L
    nsv6030918copy number variation1nstd212human GRCh38 chr15: 63,149,543-63,149,620 , GRCh37.p13 chr15: 63,441,742-63,441,819 RPS27L
    nsv5975502insertion1nstd209human GRCh38 chr15: 63,146,250-63,146,250 , GRCh37.p13 chr15: 63,438,449-63,438,449 RPS27L
    nsv5703910mobile element insertion1nstd211human GRCh38 chr15: 63,149,601-63,149,601 , GRCh37.p13 chr15: 63,441,800-63,441,800 RPS27L
    nsv5658582insertion1nstd207human GRCh38 chr15: 63,146,250-63,146,250 , GRCh37.p13 chr15: 63,438,449-63,438,449 RPS27L
    nsv5586014copy number variation1nstd207human GRCh38 chr15: 63,149,543-63,149,619 , GRCh37.p13 chr15: 63,441,742-63,441,818 RPS27L
    nsv5538320insertion1nstd206human GRCh38 chr15: 63,146,281-63,146,301 , GRCh37.p13 chr15: 63,438,480-63,438,500 RPS27L
    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