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Items: 1 to 20 of 21

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094170copy number variation1nstd102humanUncertain significance GRCh37 chr11: 46,387,807-46,401,497 , GRCh38.p12 chr11: 46,366,257-46,379,947 DGKZ, MDK, 1 more genes
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 DGKZ, FAUP4, 2031 more genes
    nsv3922177copy number variation1nstd102humanPathogenic GRCh38 chr11: 35,663,578-46,959,820 , GRCh37 chr11: 35,685,126-46,981,371 , NCBI36 chr11: 35,641,702-46,937,947 DGKZ, MIR3160-2, 122 more genes
    nsv3913842copy number variation1nstd102humanPathogenic GRCh37 chr11: 39,200,802-49,157,287 , NCBI36 chr11: 39,157,378-49,113,863 , GRCh38 chr11: 39,179,252-49,135,735 DGKZ, MIR3160-1, 162 more genes
    nsv3924778copy number variation1nstd102humanPathogenic GRCh38 chr11: 41,118,322-48,643,003 , GRCh37 chr11: 41,139,872-48,664,555 , NCBI36 chr11: 41,096,448-48,621,131 DGKZ, F2, 140 more genes
    nsv6291196copy number variation1nstd102humanPathogenic GRCh37 chr11: 40,117,145-46,920,718 , GRCh38.p12 chr11: 40,095,595-46,899,167 DGKZ, LINC02687, 86 more genes
    nsv6309196copy number variation1nstd102humanPathogenic GRCh37 chr11: 45,827,353-46,401,497 , GRCh38.p12 chr11: 45,805,802-46,379,947 DGKZ, LINC02710, 14 more genes
    nsv3893233copy number variation1nstd102humanPathogenic GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576 DGKZ, LOC105376598, 2842 more genes
    nsv3900144copy number variation1nstd102humanPathogenic GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169 DGKZ, RTN3, 2833 more genes
    nsv3908873copy number variation2nstd102humanPathogenic GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576 DGKZ, IGHMBP2, 2829 more genes
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 DGKZ, PYGM, 2125 more genes
    nsv6315474copy number variation1nstd102humanPathogenic GRCh37 chr11: 43,607,886-61,466,671 , GRCh38.p12 chr11: 43,586,336-61,699,199 DGKZ, TRR-TCT3-2, 494 more genes
    nsv5380725copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr11: 45,827,353-47,804,770 , GRCh38.p12 chr11: 45,805,802-47,783,218 DGKZ, MIR4688, 58 more genes
    nsv4729122copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 45,995,260-46,536,343 , GRCh38.p12 chr11: 45,973,709-46,514,793 DGKZ, CHRM4, 13 more genes
    nsv3914563copy number variation1nstd102humanLikely pathogenic NCBI36 chr11: 42,705,681-49,113,863 , GRCh37 chr11: 42,749,105-49,157,287 , GRCh38 chr11: 42,727,555-49,135,735 DGKZ, ACP2, 143 more genes
    nsv6313964copy number variation1nstd102humanUncertain significance GRCh37 chr11: 46,248,477-46,748,132 , GRCh38.p12 chr11: 46,226,926-46,726,582 DGKZ, ARHGAP1, 13 more genes
    nsv4456633copy number variation1nstd102humanUncertain significance GRCh37 chr11: 46,302,171-46,783,079 , GRCh38.p12 chr11: 46,280,620-46,761,529 DGKZ, MIR5582, 15 more genes
    nsv6309197copy number variation1nstd102humanUncertain significance GRCh37 chr11: 46,318,032-46,761,066 , GRCh38.p12 chr11: 46,296,481-46,739,516 DGKZ, MIR3160-2, 12 more genes
    nsv4683154copy number variation1nstd102humanUncertain significance GRCh37 chr11: 46,387,807-46,766,127 , GRCh38.p12 chr11: 46,366,257-46,744,577 DGKZ, HARBI1, 12 more genes
    nsv4729454copy number variation1nstd102humanUncertain significance GRCh37 chr11: 46,123,974-46,442,526 , GRCh38.p12 chr11: 46,102,423-46,420,976 DGKZ, CHRM4, 10 more genes
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