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Items: 1 to 20 of 62

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5927454copy number variation1nstd209human GRCh38 chr11: 11,783,035-11,783,162 , GRCh37.p13 chr11: 11,804,582-11,804,709 MIR8070
    nsv5695776mobile element insertion1nstd211human GRCh38 chr11: 11,782,404-11,782,404 , GRCh37.p13 chr11: 11,803,951-11,803,951 MIR8070
    nsv5411426mobile element insertion1nstd206human GRCh38 chr11: 11,782,404-11,782,455 , GRCh37.p13 chr11: 11,803,951-11,804,002 MIR8070
    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
    nsv4674824copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,053,978-34,732,891 , GRCh38.p12 chr11: 11,032,431-34,711,344 SNORA88, LINC02729, 305 more genes
    nsv4455732copy number variation1nstd102humanUncertain significance GRCh37 chr11: 11,461,387-12,258,307 , GRCh38.p12 chr11: 11,439,840-12,236,760 LINC02547, LOC107984311, 10 more genes
    nsv4371846copy number variation1nstd173human GRCh37 chr11: 11,731,690-12,561,676 , GRCh38.p12 chr11: 11,710,143-12,540,129 , H3P33, 9 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
    nsv4202371copy number variation1nstd166human GRCh37.p13 chr11: 11,728,300-11,845,240 , GRCh38.p12 chr11: 11,706,753-11,823,693 LOC107984311, MIR8070
    nsv4201319copy number variation1nstd166human GRCh37.p13 chr11: 11,804,695-11,804,826 , GRCh38.p12 chr11: 11,783,148-11,783,279 MIR8070
    nsv3963651copy number variation1nstd168human GRCh38 chr11: 11,769,676-11,823,050 , GRCh37.p13 chr11: 11,791,223-11,844,597 MIR8070, LOC107984311
    nsv3915585copy number variation1nstd102humanPathogenic NCBI36 chr11: 9,967,639-16,803,929 , GRCh37 chr11: 10,011,063-16,847,353 , GRCh38 chr11: 9,989,516-16,825,806 BTBD10, LOC107984370, 86 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
    nsv3912175copy number variation1nstd102humanPathogenic NCBI36 chr11: 10,107,142-14,047,625 , GRCh37.p13 chr11: 10,150,566-14,091,049 , GRCh38.p12 chr11: 10,129,019-14,069,502 LINC02545, CENPUP1, 58 more genes
    nsv3908873copy number variation2nstd102humanPathogenic GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576 IGHMBP2, SYTL2, 2829 more genes
    nsv3906221copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-31,995,219 , GRCh38.p12 chr11: 230,615-31,973,673 PCNAP4, LIN7C, 688 more genes
    nsv3900144copy number variation1nstd102humanPathogenic GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169 RTN3, KRTAP5-13P, 2833 more genes
    nsv3898948copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-17,099,213 , GRCh38.p12 chr11: 230,615-17,077,666 MTND5P21, IFITM1, 506 more genes
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