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 573

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094433copy number variation1nstd102humanPathogenic GRCh37 chr14: 54,410,919-55,369,403 , GRCh38.p12 chr14: 53,944,201-54,902,685 BMP4, MIR5580, 14 more genes
    nsv7076330inversion1nstd229human GRCh38 chr14: 54,613,542-54,620,168 , GRCh37.p13 chr14: 55,080,260-55,086,886 LOC112268133, SAMD4A
    nsv7071352inversion1nstd229human GRCh38 chr14: 54,647,125-54,647,461 , GRCh37.p13 chr14: 55,113,843-55,114,179 SAMD4A
    nsv7071038inversion1nstd229human GRCh38 chr14: 54,784,222-54,784,344 , GRCh37.p13 chr14: 55,250,940-55,251,062 SAMD4A
    nsv7063700inversion1nstd229human GRCh38 chr14: 48,591,726-55,698,685 , GRCh37.p13 chr14: 49,060,929-56,165,403 ZFP64P1, LINC02331, 132 more genes
    nsv7060471inversion1nstd229human GRCh38 chr14: 54,671,401-63,742,041 , GRCh37.p13 chr14: 55,138,119-64,208,759 KTN1, OTX2-AS1, 153 more genes
    nsv7059291inversion1nstd229human GRCh38 chr14: 49,838,942-56,572,993 , GRCh37.p13 chr14: 50,305,660-57,039,711 LOC105370500, LINC01599, 124 more genes
    nsv6956646copy number variation1nstd229human GRCh38 chr14: 54,640,246-54,645,272 , GRCh37.p13 chr14: 55,106,964-55,111,990 SAMD4A
    nsv6955746copy number variation1nstd229human GRCh38 chr14: 54,679,780-54,682,889 , GRCh37.p13 chr14: 55,146,498-55,149,607 SAMD4A-AS1, SAMD4A
    nsv6955559copy number variation1nstd229human GRCh38 chr14: 54,577,431-54,580,143 , GRCh37.p13 chr14: 55,044,149-55,046,861 SAMD4A
    nsv6954931copy number variation1nstd229human GRCh38 chr14: 54,697,143-54,699,777 , GRCh37.p13 chr14: 55,163,861-55,166,495 SAMD4A
    nsv6954825copy number variation1nstd229human GRCh38 chr14: 54,602,422-54,605,895 , GRCh37.p13 chr14: 55,069,140-55,072,613 LOC112268133, SAMD4A
    nsv6954729copy number variation1nstd229human GRCh38 chr14: 54,707,137-54,710,163 , GRCh37.p13 chr14: 55,173,855-55,176,881 SAMD4A
    nsv6953900copy number variation1nstd229human GRCh38 chr14: 54,761,162-54,761,245 , GRCh37.p13 chr14: 55,227,880-55,227,963 SAMD4A
    nsv6953422copy number variation1nstd229human GRCh38 chr14: 54,738,008-54,740,166 , GRCh37.p13 chr14: 55,204,726-55,206,884 SAMD4A
    nsv6953179copy number variation1nstd229human GRCh38 chr14: 54,229,437-54,576,363 , GRCh37.p13 chr14: 54,696,155-55,043,081 CGRRF1, CDKN3, 3 more genes
    nsv6953159copy number variation1nstd229human GRCh38 chr14: 54,640,965-54,647,104 , GRCh37.p13 chr14: 55,107,683-55,113,822 SAMD4A
    nsv6952857copy number variation1nstd229human GRCh38 chr14: 54,507,957-54,626,218 , GRCh37.p13 chr14: 54,974,675-55,092,936 LOC112268133, CGRRF1, 1 more genes
    nsv6952487copy number variation1nstd229human GRCh38 chr14: 54,749,906-54,753,739 , GRCh37.p13 chr14: 55,216,624-55,220,457 SAMD4A
    nsv6951963copy number variation1nstd229human GRCh38 chr14: 54,735,442-54,738,935 , GRCh37.p13 chr14: 55,202,160-55,205,653 SAMD4A
    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