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 171

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093918copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr11: 116,660,844-117,870,356 , GRCh38.p12 chr11: 116,790,128-117,999,641 PAFAH1B2, FXYD2, 26 more genes
    nsv7093833copy number variation6nstd102humanUncertain significance GRCh37 chr11: 116,691,583-121,500,272 , GRCh38.p12 chr11: 116,820,867-121,629,563 RN7SL688P, MIR4492, 131 more genes
    nsv7093753copy number variation1nstd102humanUncertain significance GRCh37 chr11: 117,209,303-120,133,495 , GRCh38.p12 chr11: 117,338,587-120,262,786 TMEM25, HYOU1, 93 more genes
    nsv7062420inversion1nstd229human GRCh38 chr11: 117,681,463-119,526,734 , GRCh37.p13 chr11: 117,552,178-119,397,444 RN7SL688P, MIR4492, 72 more genes
    nsv7060960inversion1nstd229human GRCh38 chr11: 117,860,307-117,864,995 , GRCh37.p13 chr11: 117,731,022-117,735,710 FXYD6, FXYD6-FXYD2
    nsv6913482copy number variation1nstd229human GRCh38 chr11: 117,875,901-117,877,300 , GRCh37.p13 chr11: 117,746,616-117,748,015 FXYD6-FXYD2, FXYD6
    nsv6912121copy number variation1nstd229human GRCh38 chr11: 117,857,085-117,947,826 , GRCh37.p13 chr11: 117,727,800-117,818,541 FXYD6, TMPRSS13, 1 more genes
    nsv6902051copy number variation1nstd229human GRCh38 chr11: 117,622,062-117,860,669 , GRCh37.p13 chr11: 117,492,777-117,731,384 FXYD2, DSCAML1, 3 more genes
    nsv6900844copy number variation1nstd229human GRCh38 chr11: 117,859,343-117,861,861 , GRCh37.p13 chr11: 117,730,058-117,732,576 FXYD6-FXYD2, FXYD6
    nsv6899779copy number variation1nstd229human GRCh38 chr11: 117,824,625-117,854,524 , GRCh37.p13 chr11: 117,695,340-117,725,239 FXYD2, FXYD6, 1 more genes
    nsv6584509inversion1nstd223human GRCh38 chr11: 117,856,557-117,860,923 , GRCh37.p13 chr11: 117,727,272-117,731,638 FXYD6-FXYD2, FXYD6
    nsv6465083copy number variation1nstd223human GRCh38 chr11: 117,833,481-117,835,004 , GRCh37.p13 chr11: 117,704,196-117,705,719 FXYD6, FXYD6-FXYD2
    nsv6464246copy number variation1nstd223human GRCh38 chr11: 117,857,085-117,947,830 , GRCh37.p13 chr11: 117,727,800-117,818,545 FXYD6-FXYD2, TMPRSS13, 1 more genes
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6308962copy number variation1nstd102humanUncertain significance GRCh37 chr11: 116,660,844-121,500,272 , GRCh38.p12 chr11: 116,790,128-121,629,563 LOC107984399, PCSK7, 132 more genes
    nsv6291074copy number variation1nstd102humanPathogenic GRCh37 chr11: 112,375,478-128,785,742 , GRCh38.p12 chr11: 112,504,755-128,915,847 ZW10, MPZL2, 378 more genes
    nsv6290834copy number variation1nstd102humanUncertain significance GRCh37 chr11: 85,422,071-118,022,671 , GRCh38.p12 chr11: 85,711,028-118,151,956 CARD17P, RNA5SP350, 480 more genes
    nsv6289927copy number variation1nstd102humanPathogenic GRCh37 chr11: 104,288,964-134,937,416 , GRCh38.p12 chr11: 104,418,236-135,067,522 IGSF9B, MIR10526, 592 more genes
    nsv6131836copy number variation1nstd213human GRCh37 chr11: 117,740,000-117,930,001 , GRCh38.p12 chr11: 117,869,285-118,059,286 IL10RA, FXYD6, 3 more genes
    nsv5500379copy number variation1nstd206human GRCh38 chr11: 117,867,187-117,872,813 , GRCh37.p13 chr11: 117,737,902-117,743,528 FXYD6-FXYD2, FXYD6
    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