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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5923295copy number variation1nstd209human GRCh38 chr11: 59,127,677-59,133,064 , GRCh37.p13 chr11: 58,895,150-58,900,537 FAM111B, FAM111A-DT
    nsv5853937copy number variation1nstd209human GRCh38 chr11: 59,120,044-59,133,160 , GRCh37.p13 chr11: 58,887,517-58,900,633 FAM111A-DT, FAM111B
    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
    nsv5326104inversion1nstd204human GRCh37.p13 chr11: 58,446,123-60,252,987 , GRCh38.p13 chr11: 58,678,650-60,485,514 OSBP, OR5BB1P, 78 more genes
    nsv5325627inversion1nstd204human GRCh37.p13 chr11: 58,669,453-61,321,541 , GRCh38.p13 chr11: 58,901,980-61,554,069 , CD5, 118 more genes
    nsv4984973copy number variation1nstd200human GRCh38 chr11: 58,629,506-59,462,358 , GRCh37.p13 chr11: 58,396,979-59,229,831 GLYATL1P4, LOC283194, 29 more genes
    nsv4979571copy number variation1nstd200human GRCh38 chr11: 59,135,955-59,145,275 , GRCh37.p13 chr11: 58,903,428-58,912,748 FAM111A, FAM111A-DT, 1 more genes
    nsv4885672inversion1nstd200human GRCh37 chr11: 58,669,461-61,321,541 , GRCh38.p12 chr11: 58,901,988-61,554,069 , MS4A2, 118 more genes
    nsv4870911inversion1nstd200human GRCh37 chr11: 58,446,132-60,252,987 , GRCh38.p12 chr11: 58,678,659-60,485,514 LOC100422398, LOC100287485, 78 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
    nsv4729406copy number variation1nstd102humanUncertain significance GRCh37 chr11: 58,602,498-59,091,934 , GRCh38.p12 chr11: 58,835,025-59,324,461 LOC100422398, LOC643709, 20 more genes
    nsv4198799copy number variation1nstd166human GRCh37.p13 chr11: 58,900,917-58,900,969 , GRCh38.p12 chr11: 59,133,444-59,133,496 FAM111A-DT
    nsv3955257copy number variation1nstd168human GRCh38 chr11: 59,098,072-59,178,111 , GRCh37.p13 chr11: 58,865,545-58,945,584 DTX4, FAM111A, 4 more genes
    nsv3919875copy number variation1nstd102humanUncertain significance NCBI36 chr11: 58,548,837-58,678,418 , GRCh37.p13 chr11: 58,792,261-58,921,842 , GRCh38.p12 chr11: 59,024,788-59,154,369 GLYATL1P4, LOC283194, 6 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
    nsv3904152copy number variation1nstd102humanUncertain significance GRCh37 chr11: 49,313,405-59,008,426 , GRCh38.p12 chr11: 49,291,853-59,240,953 FAM111B, OR5M1, 250 more genes
    nsv3902441copy number variation1nstd102humanBenign GRCh37 chr11: 58,846,985-59,065,644 , GRCh38.p12 chr11: 59,079,512-59,298,171 LOC100422399, FAM111A-DT, 11 more genes
    nsv3900144copy number variation1nstd102humanPathogenic GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169 RTN3, KRTAP5-13P, 2833 more genes
    nsv3893233copy number variation1nstd102humanPathogenic GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576 LOC105376598, OSBPL9P2, 2842 more genes
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