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Items: 1 to 20 of 261

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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
    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
    nsv6913109copy number variation1nstd229human GRCh38 chr11: 18,569,903-18,577,606 , GRCh37.p13 chr11: 18,591,450-18,599,153 UEVLD
    nsv6912968copy number variation1nstd229human GRCh38 chr11: 18,571,601-18,574,800 , GRCh37.p13 chr11: 18,593,148-18,596,347 UEVLD
    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
    nsv6910006copy number variation1nstd229human GRCh38 chr11: 18,558,536-18,562,430 , GRCh37.p13 chr11: 18,580,083-18,583,977 UEVLD
    nsv6909873copy number variation1nstd229human GRCh38 chr11: 18,571,587-18,574,781 , GRCh37.p13 chr11: 18,593,134-18,596,328 UEVLD
    nsv6909665copy number variation1nstd229human GRCh38 chr11: 18,536,956-18,542,893 , GRCh37.p13 chr11: 18,558,503-18,564,440 UEVLD
    nsv6901284copy number variation1nstd229human GRCh38 chr11: 18,572,570-18,577,599 , GRCh37.p13 chr11: 18,594,117-18,599,146 UEVLD
    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
    nsv6592696inversion1nstd223human GRCh38 chr11: 18,565,666-18,566,065 , GRCh37.p13 chr11: 18,587,213-18,587,612 UEVLD
    nsv6590311inversion1nstd223human GRCh38 chr11: 16,144,251-19,584,623 , GRCh37.p13 chr11: 16,165,797-19,606,170 LDHC, GLTPP1, 85 more genes
    nsv6588724inversion1nstd223human GRCh38 chr11: 18,552,938-18,554,368 , GRCh37.p13 chr11: 18,574,485-18,575,915 UEVLD
    nsv6587233inversion1nstd223human GRCh38 chr11: 18,553,152-18,554,091 , GRCh37.p13 chr11: 18,574,699-18,575,638 UEVLD
    nsv6582475inversion1nstd223human GRCh38 chr11: 18,572,689-18,574,397 , GRCh37.p13 chr11: 18,594,236-18,595,944 UEVLD
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