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Items: 1 to 20 of 139

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5500605copy number variation1nstd206human GRCh38 chr11: 4,497,019-4,567,709 , GRCh37.p13 chr11: 4,518,249-4,588,939 OR52M1, OR52M2P
    nsv5306444copy number variation1nstd204human GRCh38.p13 chr11: 4,536,194-4,563,706 , GRCh37.p13 chr11: 4,557,424-4,584,936 OR52M1
    nsv5256327copy number variation1nstd204human GRCh38.p13 chr11: 4,535,390-4,559,949 , GRCh37.p13 chr11: 4,556,620-4,581,179 OR52M1
    nsv5251636copy number variation1nstd204human GRCh38.p13 chr11: 4,524,901-4,620,000 , GRCh37.p13 chr11: 4,546,131-4,641,230 OR52I2, OR52M1, 3 more genes
    nsv5251108copy number variation1nstd204human GRCh38.p13 chr11: 4,536,201-4,563,700 , GRCh37.p13 chr11: 4,557,431-4,584,930 OR52M1
    nsv4977962copy number variation1nstd200human GRCh38 chr11: 4,536,189-4,563,691 , GRCh37.p13 chr11: 4,557,419-4,584,921 OR52M1
    nsv4977961copy number variation1nstd200human GRCh38 chr11: 4,521,621-4,567,481 , GRCh37.p13 chr11: 4,542,851-4,588,711 OR52M1
    nsv4977959copy number variation1nstd200human GRCh38 chr11: 4,516,868-4,552,681 , GRCh37.p13 chr11: 4,538,098-4,573,911 OR52M1
    nsv4977956copy number variation1nstd200human GRCh38 chr11: 4,497,019-4,567,709 , GRCh37.p13 chr11: 4,518,249-4,588,939 OR52M1, OR52M2P
    nsv4977955copy number variation1nstd200human GRCh38 chr11: 4,495,092-4,614,586 , GRCh37.p13 chr11: 4,516,322-4,635,816 TRIM68, OR52M1, 4 more genes
    nsv4977953copy number variation1nstd200human GRCh38 chr11: 4,449,871-4,656,651 , GRCh37.p13 chr11: 4,471,101-4,677,881 OR52M1, OR52K1, 9 more genes
    nsv4841471copy number variation1nstd200human GRCh37 chr11: 4,503,653-4,587,528 , GRCh38.p12 chr11: 4,482,423-4,566,298 OR52M2P, OR52M1, 1 more genes
    nsv4833395copy number variation1nstd200human GRCh37 chr11: 4,557,419-4,584,920 , GRCh38.p12 chr11: 4,536,189-4,563,690 OR52M1
    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
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4729112copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-4,851,537 , GRCh38.p12 chr11: 230,615-4,830,307 OR51E1, TNNI2, 203 more genes
    nsv4728922copy number variation1nstd102humanUncertain significance GRCh37 chr11: 4,388,904-4,639,840 , GRCh38.p12 chr11: 4,367,674-4,618,610 OR52K1, OR52B4, 12 more genes
    nsv4679088copy number variation1nstd189human GRCh37.p13 chr11: 4,335,879-4,833,224 , GRCh38.p12 chr11: 4,314,649-4,811,994 TRIM21, TRIM68, 29 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
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