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 78

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5496438copy number variation1nstd206human GRCh38 chr11: 4,912,950-4,915,854 , GRCh37.p13 chr11: 4,934,180-4,937,084 OR51G2
    nsv5191436mobile element insertion1nstd203human GRCh38 chr11: 4,913,372-4,913,385 , GRCh37.p13 chr11: 4,934,602-4,934,615 OR51G2
    nsv4768373copy number variation1nstd102humanPathogenic GRCh37 chr11: 210,300-8,664,358 , GRCh38.p12 chr11: 210,300-8,642,811 LOC107984302, STK33, 375 more genes
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4674879copy number variation1nstd102humanPathogenic GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449 BGLT3, RPL21P97, 723 more genes
    nsv4607020copy number variation1nstd183human GRCh37 chr11: 4,928,585-4,968,117 , GRCh38.p12 chr11: 4,907,355-4,946,887 OR51G2, OR51A4, 3 more genes
    nsv4567719mobile element insertion1nstd166human GRCh37.p13 chr11: 4,934,602-4,934,602 , GRCh38.p12 chr11: 4,913,372-4,913,372 OR51G2
    nsv4382560copy number variation1nstd173human GRCh37 chr11: 4,687,080-4,967,238 , GRCh38.p12 chr11: 4,665,850-4,946,008 OR51N1P, OR51A8P, 22 more genes
    nsv4381756copy number variation1nstd173human GRCh37 chr11: 4,167,416-5,153,276 , GRCh38.p12 chr11: 4,146,186-5,132,046 C11orf40, OR51H1, 62 more genes
    nsv4350476copy number variation1nstd102humanPathogenic GRCh37 chr11: 193,146-12,643,136 , GRCh38.p12 chr11: 193,146-12,621,589 KRTAP5-3, OR56A7P, 457 more genes
    nsv4209339copy number variation1nstd166human GRCh37.p13 chr11: 4,936,979-4,937,076 , GRCh38.p12 chr11: 4,915,749-4,915,846 OR51G2
    nsv4197040copy number variation1nstd166human GRCh37.p13 chr11: 4,920,741-4,987,613 , GRCh38.p12 chr11: 4,899,511-4,966,383 OR51G1, OR51A3P, 4 more genes
    nsv4192783copy number variation1nstd166human GRCh37.p13 chr11: 4,640,331-5,290,171 , GRCh38.p12 chr11: 4,619,101-5,268,941 HBE1, OR52E1, 50 more genes
    nsv3962153copy number variation1nstd168human GRCh38 chr11: 4,914,682-4,978,064 , GRCh37.p13 chr11: 4,935,912-4,999,294 OR51G1, OR51A5P, 4 more genes
    nsv3919565copy number variation1nstd102humanPathogenic GRCh38 chr11: 61,793-10,727,969 , GRCh37 chr11: 61,793-10,749,516 , NCBI36 chr11: 51,793-10,706,092 OR51A7, OR51F5P, 437 more genes
    nsv3918376copy number variation1nstd102humanPathogenic NCBI36 chr11: 128,203-5,440,733 , GRCh37.p13 chr11: 138,203-5,484,157 , GRCh38.p12 chr11: 138,203-5,462,927 HBG2, OR51T1, 262 more genes
    nsv3913735copy number variation1nstd102humanPathogenic GRCh37 chr11: 196,855-5,343,104 , GRCh38 chr11: 196,855-5,321,874 , NCBI36 chr11: 186,855-5,299,680 CDKN1C, LOC107984301, 246 more genes
    nsv3912558copy number variation1nstd102humanPathogenic GRCh37 chr11: 446,754-18,926,289 , GRCh38 chr11: 446,754-18,904,742 , NCBI36 chr11: 436,754-18,882,865 TRIM22, CSNK2A3, 546 more genes
    nsv3912125copy number variation1nstd102humanUncertain significance NCBI36 chr11: 3,949,918-4,989,260 , GRCh37.p13 chr11: 3,993,342-5,032,684 , GRCh38.p12 chr11: 3,972,112-5,011,454 OR51G2, SSU72L3, 57 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