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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5507269copy number variation1nstd206human GRCh38 chr11: 43,929,325-43,946,240 , GRCh37.p13 chr11: 43,950,875-43,967,790 C11orf96
    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
    nsv4987242copy number variation1nstd200human GRCh38 chr11: 43,710,265-43,953,275 , GRCh37.p13 chr11: 43,731,815-43,974,825 HSD17B12, ALKBH3, 7 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
    nsv4729468copy number variation1nstd102humanUncertain significance GRCh37 chr11: 43,223,479-44,266,544 , GRCh38.p12 chr11: 43,201,929-44,244,994 MIR670, ALKBH3, 18 more genes
    nsv4710519copy number variation1nstd195human GRCh37 chr11: 43,800,201-44,412,451 , GRCh38.p12 chr11: 43,778,651-44,390,901 ACCSL, HSD17B12, 9 more genes
    nsv4675989copy number variation1nstd102humanUncertain significance GRCh37 chr11: 43,757,860-44,118,731 , GRCh38.p12 chr11: 43,736,310-44,097,181 SEC14L1P1, EXT2, 8 more genes
    nsv4675717copy number variation1nstd102humanUncertain significance GRCh37 chr11: 43,664,817-44,889,240 , GRCh38.p12 chr11: 43,643,267-44,867,689 C11orf96, ACCSL, 17 more genes
    nsv4455217copy number variation1nstd102humanUncertain significance GRCh37 chr11: 43,732,634-43,973,830 , GRCh38.p12 chr11: 43,711,084-43,952,280 C11orf96, SEC14L1P1, 7 more genes
    nsv4428743copy number variation1nstd174human GRCh37 chr11: 43,946,939-43,969,231 , GRCh38.p12 chr11: 43,925,389-43,947,681 C11orf96
    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 F2, PSMC3, 140 more genes
    nsv3924016copy number variation1nstd102humanLikely pathogenic NCBI36 chr11: 40,666,800-44,162,262 , GRCh37 chr11: 40,710,224-44,205,686 , GRCh38 chr11: 40,688,674-44,184,136 EXT2, API5, 29 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 MIR3160-2, LOC105376631, 122 more genes
    nsv3921841copy number variation1nstd102humanPathogenic NCBI36 chr11: 42,531,785-46,092,919 , GRCh37 chr11: 42,575,209-46,136,343 , GRCh38 chr11: 42,553,659-46,114,792 PEX16, LOC105376655, 51 more genes
    nsv3921625copy number variation1nstd102humanUncertain significance GRCh37 chr11: 40,710,224-44,934,960 , NCBI36 chr11: 40,666,800-44,891,536 , GRCh38 chr11: 40,688,674-44,913,409 CTBP2P6, SEC14L1P1, 36 more genes
    nsv3917236copy number variation1nstd102humanPathogenic GRCh37 chr11: 39,706,376-44,866,811 , GRCh38 chr11: 39,684,826-44,845,260 , NCBI36 chr11: 39,662,952-44,823,387 LOC107984328, LRRC4C, 42 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 ACP2, ARHGAP1, 143 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 MIR3160-1, RPS20P26, 162 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
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