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Items: 1 to 20 of 118

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093841copy number variation1nstd102humanUncertain significance GRCh37 chr11: 18,418,390-19,204,313 , GRCh38.p12 chr11: 18,396,843-19,182,766 UEVLD, ZDHHC13, 25 more genes
    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
    nsv6912848copy number variation1nstd229human GRCh38 chr11: 18,584,654-18,600,225 , GRCh37.p13 chr11: 18,606,201-18,621,772 UEVLD, LOC112268073, 2 more genes
    nsv6898753copy number variation1nstd229human GRCh38 chr11: 18,571,281-18,602,891 , GRCh37.p13 chr11: 18,592,828-18,624,438 UEVLD, MTCH1P2, 2 more genes
    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
    nsv6637387copy number variation1nstd102humanUncertain significance GRCh37 chr11: 18,585,628-18,692,833 , GRCh38.p12 chr11: 18,564,081-18,671,286 SPTY2D1, MTCH1P2, 5 more genes
    nsv6637210copy number variation1nstd102humanUncertain significance GRCh37 chr11: 18,582,223-18,697,956 , GRCh38.p12 chr11: 18,560,676-18,676,409 SPTY2D1, MTCH1P2, 5 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
    nsv6588337inversion1nstd223human GRCh38 chr11: 18,598,342-18,600,424 , GRCh37.p13 chr11: 18,619,889-18,621,971 LOC112268073, MISFA
    nsv6585463inversion1nstd223human GRCh38 chr11: 18,604,980-18,605,702 , GRCh37.p13 chr11: 18,626,527-18,627,249 SPTY2D1, MISFA
    nsv6449627copy number variation1nstd223human GRCh38 chr11: 18,584,707-18,600,214 , GRCh37.p13 chr11: 18,606,254-18,621,761 MTCH1P2, MISFA, 2 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
    nsv6314200copy number variation1nstd102humanUncertain significance GRCh37 chr11: 18,482,438-18,792,764 , GRCh38.p12 chr11: 18,460,891-18,771,217 LDHAL6A, SPTY2D1, 11 more genes
    nsv6274718copy number variation1nstd214human GRCh38 chr11: 18,606,990-18,607,126 , GRCh37.p13 chr11: 18,628,537-18,628,673 SPTY2D1, MISFA
    nsv6207126copy number variation1nstd214human GRCh38 chr11: 18,608,921-18,608,985 , GRCh37.p13 chr11: 18,630,468-18,630,532 SPTY2D1, MISFA
    nsv5971404insertion1nstd209human GRCh38 chr11: 18,610,686-18,610,686 , GRCh37.p13 chr11: 18,632,233-18,632,233 SPTY2D1, MISFA
    nsv5923520copy number variation1nstd209human GRCh38 chr11: 18,608,921-18,608,985 , GRCh37.p13 chr11: 18,630,468-18,630,532 SPTY2D1, MISFA
    nsv5909105copy number variation1nstd209human GRCh38 chr11: 18,584,644-18,600,213 , GRCh37.p13 chr11: 18,606,191-18,621,760 UEVLD, MTCH1P2, 2 more genes
    nsv5604010copy number variation1nstd207human GRCh38 chr11: 18,608,921-18,608,985 , GRCh37.p13 chr11: 18,630,468-18,630,532 SPTY2D1, MISFA
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