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Items: 1 to 20 of 141

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5504445copy number variation1nstd206human GRCh38 chr11: 33,724,142-33,724,215 , GRCh37.p13 chr11: 33,745,688-33,745,761 CD59
    nsv5502810copy number variation1nstd206human GRCh38 chr11: 33,734,067-33,738,641 , GRCh37.p13 chr11: 33,755,613-33,760,187 CD59
    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
    nsv5305252copy number variation1nstd204human GRCh38.p13 chr11: 33,703,675-33,707,895 , GRCh37.p13 chr11: 33,725,221-33,729,441 CD59
    nsv5277384copy number variation1nstd204human GRCh38.p13 chr11: 33,701,601-33,707,900 , GRCh37.p13 chr11: 33,723,147-33,729,446 C11orf91, CD59
    nsv5271032copy number variation1nstd204human GRCh38.p13 chr11: 33,703,948-33,707,952 , GRCh37.p13 chr11: 33,725,494-33,729,498 CD59
    nsv4986997copy number variation1nstd200human GRCh38 chr11: 33,703,661-33,707,894 , GRCh37.p13 chr11: 33,725,207-33,729,440 CD59
    nsv4984376copy number variation1nstd200human GRCh38 chr11: 33,703,665-33,707,882 , GRCh37.p13 chr11: 33,725,211-33,729,428 CD59
    nsv4834104copy number variation1nstd200human GRCh37 chr11: 33,725,149-33,729,462 , GRCh38.p12 chr11: 33,703,603-33,707,916 CD59
    nsv4832979copy number variation1nstd200human GRCh37 chr11: 33,725,207-33,729,447 , GRCh38.p12 chr11: 33,703,661-33,707,901 CD59
    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
    nsv4675518copy number variation1nstd102humanUncertain significance GRCh37 chr11: 33,221,821-34,569,417 , GRCh38.p12 chr11: 33,200,275-34,547,870 HIPK3, C11orf91, 20 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
    nsv4674824copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,053,978-34,732,891 , GRCh38.p12 chr11: 11,032,431-34,711,344 SNORA88, LINC02729, 305 more genes
    nsv4576103mobile element insertion1nstd166human GRCh37.p13 chr11: 33,735,930-33,735,930 , GRCh38.p12 chr11: 33,714,384-33,714,384 CD59
    nsv4567827mobile element insertion1nstd166human GRCh37.p13 chr11: 33,758,241-33,758,241 , GRCh38.p12 chr11: 33,736,695-33,736,695 CD59
    nsv4455873copy number variation1nstd102humanPathogenic GRCh37 chr11: 22,079,154-35,597,645 , GRCh38.p12 chr11: 22,057,608-35,576,097 DNAJC24, LOC102723568, 153 more genes
    nsv3922794copy number variation1nstd102humanPathogenic GRCh37 chr11: 20,101,020-34,485,543 , GRCh38 chr11: 20,079,474-34,463,996 , NCBI36 chr11: 20,057,596-34,442,119 LOC107984419, LINC02758, 150 more genes
    nsv3922664copy number variation1nstd102humanPathogenic GRCh38 chr11: 22,550,115-38,199,159 , NCBI36 chr11: 22,528,237-38,177,285 , GRCh37 chr11: 22,571,661-38,220,709 CSTF3, LOC101928338, 170 more genes
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