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Items: 1 to 20 of 97

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    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
    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
    nsv4685714copy number variation1nstd102humannot provided GRCh37 chr11: 58,237,819-58,800,374 , GRCh38.p12 chr11: 58,470,346-59,032,901 GLYATL1, LPXN, 14 more genes
    nsv4212058copy number variation1nstd166human GRCh37.p13 chr11: 58,425,717-58,482,017 , GRCh38.p12 chr11: 58,658,244-58,714,544 GLYAT
    nsv4210363copy number variation1nstd166human GRCh37.p13 chr11: 58,495,485-58,495,585 , GRCh38.p12 chr11: 58,728,012-58,728,112 GLYAT
    nsv4207706copy number variation1nstd166human GRCh37.p13 chr11: 58,483,577-58,779,220 , GRCh38.p12 chr11: 58,716,104-59,011,747 LOC100422398, GLYATL1, 8 more genes
    nsv4203900copy number variation1nstd166human GRCh37.p13 chr11: 58,484,199-58,488,435 , GRCh38.p12 chr11: 58,716,726-58,720,962 GLYAT
    nsv3911150copy number variation1nstd102humanPathogenic GRCh37 chr11: 55,086,995-58,766,250 , NCBI36 chr11: 54,843,571-58,522,826 , GRCh38 chr11: 55,319,519-58,998,777 OR5BD1P, SELENOH, 197 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
    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
    nsv3168776inversion1nstd158human GRCh37 chr11: 37,074,771-61,357,521 , GRCh38.p12 chr11: 37,053,221-61,590,049 , ACP2, 535 more genes
    nsv3168425copy number variation1nstd158human GRCh37 chr11: 3,543,079-67,662,509 , GRCh38.p12 chr11: 3,521,849-67,895,038 , ACP2, 1535 more genes
    nsv3156930copy number variation1nstd151human GRCh37 chr11: 58,491,886-58,607,090 , GRCh38.p12 chr11: 58,724,413-58,839,617 GLYAT, GLYATL2, 2 more genes
    nsv3140190copy number variation2nstd151human GRCh37 chr11: 58,491,886-58,723,505 , GRCh38.p12 chr11: 58,724,413-58,956,032 GLYAT, GLYATL1, 5 more genes
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