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Items: 1 to 20 of 61

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093762copy number variation1nstd102humanPathogenic GRCh37 chr11: 13,513,952-13,514,402 , GRCh38.p12 chr11: 13,492,405-13,492,855 PTH
    nsv7070306inversion1nstd229human GRCh38 chr11: 13,396,389-14,573,064 , GRCh37.p13 chr11: 13,417,936-14,594,610 LOC105376670, RRAS2, 15 more genes
    nsv7066313inversion1nstd229human GRCh38 chr11: 6,624,146-15,294,249 , GRCh37.p13 chr11: 6,645,377-15,315,795 RNA5SP332, TMEM41B, 163 more genes
    nsv6917151copy number variation1nstd229human GRCh38 chr11: 9,940,109-18,580,574 , GRCh37.p13 chr11: 9,961,656-18,602,121 MYOD1, MIR8070, 139 more genes
    nsv6578417inversion1nstd223human GRCh38 chr11: 7,263,807-16,565,752 , GRCh37.p13 chr11: 7,285,038-16,587,299 TEAD1, IRAG1, 151 more genes
    nsv6315535copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599 OR52Q1P, RNU6-593P, 630 more genes
    nsv6247789mobile element insertion1nstd215human GRCh38 chr11: 13,495,058-13,495,058 , GRCh37.p13 chr11: 13,516,605-13,516,605 PTH
    nsv5506804copy number variation1nstd206human GRCh38 chr11: 13,492,854-13,493,045 , GRCh37.p13 chr11: 13,514,401-13,514,592 PTH
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 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
    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
    nsv4456201copy number variation1nstd102humanUncertain significance GRCh37 chr11: 13,464,883-14,872,063 , GRCh38.p12 chr11: 13,443,336-14,850,517 COPB1, RNA5SP332, 18 more genes
    nsv4195559copy number variation1nstd166human GRCh37.p13 chr11: 13,515,538-13,516,878 , GRCh38.p12 chr11: 13,493,991-13,495,331 PTH
    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
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