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Items: 1 to 20 of 155

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6915437copy number variation1nstd229human GRCh38 chr11: 33,146,083-33,870,045 , GRCh37.p13 chr11: 33,167,629-33,891,591 LMO2, LOC105376617, 13 more genes
    nsv6908055copy number variation1nstd229human GRCh38 chr11: 33,700,201-33,701,100 , GRCh37.p13 chr11: 33,721,747-33,722,646 CD59, C11orf91
    nsv6907177copy number variation1nstd229human GRCh38 chr11: 33,714,716-33,835,724 , GRCh37.p13 chr11: 33,736,262-33,857,270 SPICP1, CD59, 4 more genes
    nsv6906705copy number variation1nstd229human GRCh38 chr11: 33,710,344-33,717,367 , GRCh37.p13 chr11: 33,731,890-33,738,913 CD59
    nsv6898567copy number variation1nstd229human GRCh38 chr11: 33,356,301-35,259,800 , GRCh37.p13 chr11: 33,377,847-35,281,347 C11orf91, EHF, 34 more genes
    nsv6638023copy number variation1nstd102humanPathogenic GRCh37 chr11: 31,372,721-38,259,316 , GRCh38.p12 chr11: 31,351,174-38,237,766 THEM7P, LOC105376624, 92 more genes
    nsv6473150copy number variation1nstd223human GRCh38 chr11: 33,699,101-33,721,880 , GRCh37.p13 chr11: 33,720,647-33,743,426 C11orf91, CD59
    nsv6472441copy number variation1nstd223human GRCh38 chr11: 33,703,723-33,707,820 , GRCh37.p13 chr11: 33,725,269-33,729,366 CD59
    nsv6467096copy number variation1nstd223human GRCh38 chr11: 33,713,804-33,714,309 , GRCh37.p13 chr11: 33,735,350-33,735,855 CD59
    nsv6460165copy number variation1nstd223human GRCh38 chr11: 33,712,024-33,712,881 , GRCh37.p13 chr11: 33,733,570-33,734,427 CD59
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6314226complex chromosomal rearrangement2nstd102humanUncertain significance GRCh37 chr11: 33,743,297-33,743,297 , GRCh37 chr11: 33,743,302-33,743,302 , GRCh37 chr11: 130,851,871-130,851,871 , GRCh37 chr11: 130,851,879-130,851,879 , GRCh38.p12 chr11: 33,721,751-33,721,751 , GRCh38.p12 chr11: 33,721,756-33,721,756 , GRCh38.p12 chr11: 130,981,976-130,981,976 , GRCh38.p12 chr11: 130,981,984-130,981,984 CD59
    nsv6304826copy number variation1nstd186human GRCh37 chr11: 33,755,613-33,760,187 , GRCh38.p12 chr11: 33,734,067-33,738,641 CD59
    nsv6131923copy number variation1nstd213human GRCh37 chr11: 33,110,000-34,110,001 , GRCh38.p12 chr11: 33,088,454-34,088,454 CD59, CSTF3, 16 more genes
    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
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