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 409

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099219copy number variation1nstd231human GRCh38.p12 chr1: 99,594,616-101,416,026 , GRCh37 chr1: 100,060,172-101,881,582 AGL, DBT, 38 more genes
    nsv7095734copy number variation1nstd102humanPathogenic GRCh37 chr1: 100,368,229-100,368,360 , GRCh38.p12 chr1: 99,902,673-99,902,804 AGL
    nsv7095733copy number variation1nstd102humanUncertain significance GRCh37 chr1: 100,327,039-100,330,165 , GRCh38.p12 chr1: 99,861,483-99,864,609 AGL
    nsv7095684copy number variation1nstd102humanPathogenic GRCh37 chr1: 100,380,935-100,382,063 , GRCh38.p12 chr1: 99,915,379-99,916,507 AGL
    nsv7095683copy number variation1nstd102humanPathogenic GRCh37 chr1: 100,366,182-100,368,360 , GRCh38.p12 chr1: 99,900,626-99,902,804 AGL
    nsv7095681copy number variation1nstd102humanUncertain significance GRCh37 chr1: 100,316,599-101,709,564 , GRCh38.p12 chr1: 99,851,043-101,244,008 SLC35A3, S1PR1-DT, 29 more genes
    nsv7095680copy number variation1nstd102humanUncertain significance GRCh37 chr1: 100,316,599-100,488,032 , GRCh38.p12 chr1: 99,851,043-100,022,476 AGL, RNU6-750P, 2 more genes
    nsv7095301copy number variation1nstd102humanPathogenic GRCh37 chr1: 100,316,589-100,483,381 , GRCh38.p12 chr1: 99,851,033-100,017,825 SLC35A3, RNU6-750P, 2 more genes
    nsv7093557insertion1nstd102humanUncertain significance GRCh38 chr1: 99,921,613-99,921,613 , GRCh37 chr1: 100,387,169-100,387,169 AGL
    nsv6658068copy number variation1nstd229human GRCh38 chr1: 99,902,295-99,907,286 , GRCh37.p13 chr1: 100,367,851-100,372,842 AGL
    nsv6658067copy number variation1nstd229human GRCh38 chr1: 99,883,897-99,884,065 , GRCh37.p13 chr1: 100,349,453-100,349,621 AGL
    nsv6658066copy number variation1nstd229human GRCh38 chr1: 99,874,614-99,874,682 , GRCh37.p13 chr1: 100,340,170-100,340,238 AGL
    nsv6658059copy number variation1nstd229human GRCh38 chr1: 99,876,636-99,907,287 , GRCh37.p13 chr1: 100,342,192-100,372,843 AGL
    nsv6657977copy number variation1nstd229human GRCh38 chr1: 99,642,179-100,077,061 , GRCh37.p13 chr1: 100,107,735-100,542,617 MFSD14A, SLC35A3, 8 more genes
    nsv6657975copy number variation1nstd229human GRCh38 chr1: 99,498,947-100,487,486 , GRCh37.p13 chr1: 99,964,503-100,953,042 CDC14A, AGL, 21 more genes
    nsv6657908copy number variation1nstd229human GRCh38 chr1: 99,866,701-99,868,800 , GRCh37.p13 chr1: 100,332,257-100,334,356 AGL
    nsv6657907copy number variation1nstd229human GRCh38 chr1: 99,850,806-99,850,881 , GRCh37.p13 chr1: 100,316,362-100,316,437 AGL
    nsv6657894copy number variation1nstd229human GRCh38 chr1: 99,356,330-99,995,147 , GRCh37.p13 chr1: 99,821,886-100,460,703 LOC107985093, LINC01708, 8 more genes
    nsv6657528copy number variation1nstd229human GRCh38 chr1: 99,924,501-100,058,000 , GRCh37.p13 chr1: 100,390,057-100,523,556 RNU6-1318P, MFSD14A, 3 more genes
    nsv6657521copy number variation1nstd229human GRCh38 chr1: 99,682,330-99,949,365 , GRCh37.p13 chr1: 100,147,886-100,414,921 PALMD, FRRS1, 4 more genes
    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