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Items: 1 to 20 of 109

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4977985copy number variation1nstd200human GRCh38 chr11: 4,990,914-5,000,154 , GRCh37.p13 chr11: 5,012,144-5,021,384 MMP26, OR51L1
    nsv4977984copy number variation1nstd200human GRCh38 chr11: 4,976,115-5,005,599 , GRCh37.p13 chr11: 4,997,345-5,026,829 OR51L1, MMP26
    nsv4977980copy number variation1nstd200human GRCh38 chr11: 4,932,439-5,055,043 , GRCh37.p13 chr11: 4,953,669-5,076,273 MMP26, OR51P1P, 7 more genes
    nsv4842046copy number variation1nstd200human GRCh37 chr11: 4,953,669-5,076,273 , GRCh38.p12 chr11: 4,932,439-5,055,043 MMP26, OR51P1P, 7 more genes
    nsv4831429copy number variation1nstd200human GRCh37 chr11: 5,012,144-5,021,384 , GRCh38.p12 chr11: 4,990,914-5,000,154 MMP26, OR51L1
    nsv4768373copy number variation1nstd102humanPathogenic GRCh37 chr11: 210,300-8,664,358 , GRCh38.p12 chr11: 210,300-8,642,811 LOC107984302, STK33, 375 more genes
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4747055copy number variation1nstd199human GRCh37 chr11: 5,008,127-5,008,187 , GRCh38.p12 chr11: 4,986,897-4,986,957 MMP26
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4729070copy number variation1nstd102humanUncertain significance GRCh37 chr11: 4,970,264-5,225,635 , GRCh38.p12 chr11: 4,949,034-5,204,405 OR52A4P, OR52J2P, 16 more genes
    nsv4680228copy number variation1nstd189human GRCh37.p13 chr11: 4,967,265-5,216,022 , GRCh38.p12 chr11: 4,946,035-5,194,792 OR52A1, OR51A1P, 16 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
    nsv4614913copy number variation1nstd183human GRCh37 chr11: 5,001,255-5,026,954 , GRCh38.p12 chr11: 4,980,025-5,005,724 MMP26, OR51L1
    nsv4604926copy number variation1nstd183human GRCh37 chr11: 4,978,382-5,038,021 , GRCh38.p12 chr11: 4,957,152-5,016,791 OR51P1P, OR51A5P, 2 more genes
    nsv4381756copy number variation1nstd173human GRCh37 chr11: 4,167,416-5,153,276 , GRCh38.p12 chr11: 4,146,186-5,132,046 C11orf40, OR51H1, 62 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
    nsv4209216copy number variation1nstd166human GRCh37.p13 chr11: 4,954,871-5,233,023 , GRCh38.p12 chr11: 4,933,641-5,211,793 OR52J1P, OR51A4, 18 more genes
    nsv4206940copy number variation1nstd166human GRCh37.p13 chr11: 4,980,843-5,188,454 , GRCh38.p12 chr11: 4,959,613-5,167,224 OR52E2, OR52A5, 12 more genes
    nsv4204350copy number variation1nstd166human GRCh37.p13 chr11: 5,007,873-5,008,390 , GRCh38.p12 chr11: 4,986,643-4,987,160 MMP26
    nsv4196538copy number variation1nstd166human GRCh37.p13 chr11: 5,011,391-5,020,040 , GRCh38.p12 chr11: 4,990,161-4,998,810 MMP26, OR51L1
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