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Items: 1 to 20 of 82

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7070173inversion1nstd229human GRCh38 chr11: 18,169,244-18,915,403 , GRCh37.p13 chr11: 18,190,791-18,936,950 TSG101, MIR3159, 33 more genes
    nsv7070030inversion1nstd229human GRCh38 chr11: 16,966,270-21,356,221 , GRCh37.p13 chr11: 16,987,817-21,377,767 DBX1, PRMT3, 93 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
    nsv6904913copy number variation1nstd229human GRCh38 chr11: 18,205,201-18,209,200 , GRCh37.p13 chr11: 18,226,748-18,230,747 SLC25A51P4
    nsv6637654copy number variation1nstd102humanUncertain significance GRCh37 chr11: 17,784,556-18,797,650 , GRCh38.p12 chr11: 17,763,009-18,776,103 LOC112268073, SAAL1, 37 more genes
    nsv6590311inversion1nstd223human GRCh38 chr11: 16,144,251-19,584,623 , GRCh37.p13 chr11: 16,165,797-19,606,170 LDHC, GLTPP1, 85 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
    nsv6281777insertion1nstd214human GRCh38 chr11: 18,209,132-18,209,132 , GRCh37.p13 chr11: 18,230,679-18,230,679 SLC25A51P4
    nsv6132091copy number variation1nstd213human GRCh37 chr11: 17,970,000-18,540,001 , GRCh38.p12 chr11: 17,948,453-18,518,454 GTF2H1, LDHA, 25 more genes
    nsv5975618insertion1nstd209human GRCh38 chr11: 18,209,132-18,209,132 , GRCh37.p13 chr11: 18,230,679-18,230,679 SLC25A51P4
    nsv5659039insertion1nstd207human GRCh38 chr11: 18,209,132-18,209,132 , GRCh37.p13 chr11: 18,230,679-18,230,679 SLC25A51P4
    nsv5545173insertion1nstd206human GRCh38 chr11: 18,209,136-18,209,183 , GRCh37.p13 chr11: 18,230,683-18,230,730 SLC25A51P4
    nsv5507673copy number variation1nstd206human GRCh38 chr11: 16,359,999-20,627,000 , GRCh37.p13 chr11: 16,381,545-20,648,546 , CSRP3, 102 more genes
    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
    nsv5380720copy number variation1nstd102humanUncertain significance GRCh37 chr11: 17,552,691-19,213,995 , GRCh38.p12 chr11: 17,531,144-19,192,448 USH1C, HIGD1AP5, 53 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
    nsv4719205insertion1nstd186human GRCh37 chr11: 18,230,679-18,230,679 , GRCh38.p12 chr11: 18,209,132-18,209,132 SLC25A51P4
    nsv4675502copy number variation1nstd102humanPathogenic GRCh37 chr11: 13,970,757-27,565,888 , GRCh38.p12 chr11: 13,949,210-27,544,341 MRGPRX5P, LDHC, 171 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
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