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Items: 1 to 20 of 118

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094093copy number variation2nstd102humanUncertain significance GRCh37 chr11: 64,973,914-70,052,579 , GRCh38.p12 chr11: 65,206,443-70,206,473 B4GAT1, CHKA-DT, 208 more genes
    nsv6913713copy number variation1nstd229human GRCh38 chr11: 67,266,401-67,465,100 , GRCh37.p13 chr11: 67,033,872-67,232,571 RNU6-1238P, TMEM134, 16 more genes
    nsv6912757copy number variation1nstd229human GRCh38 chr11: 66,793,001-68,121,500 , GRCh37.p13 chr11: 66,560,472-67,888,967 CHKA-DT, LOC107984341, 66 more genes
    nsv6905877copy number variation1nstd229human GRCh38 chr11: 60,405,001-68,536,600 , GRCh37.p13 chr11: 60,172,474-68,304,068 INCENP, SNRPCP12, 409 more genes
    nsv6898634copy number variation1nstd229human GRCh38 chr11: 67,266,601-67,521,900 , GRCh37.p13 chr11: 67,034,072-67,289,371 GRK2, CARNS1, 21 more genes
    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
    nsv6132373copy number variation1nstd213human GRCh37 chr11: 67,070,000-67,200,001 , GRCh38.p12 chr11: 67,302,529-67,432,530 RPS6KB2, SSH3, 10 more genes
    nsv6132185copy number variation1nstd213human GRCh37 chr11: 66,970,000-67,070,001 , GRCh38.p12 chr11: 67,202,529-67,302,530 GRK2, KDM2A, 2 more genes
    nsv6132112copy number variation1nstd213human GRCh37 chr11: 64,220,000-68,010,001 , GRCh38.p12 chr11: 64,452,528-68,242,533 ACTN3, ALDH3B1, 212 more genes
    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
    nsv5275203copy number variation1nstd204human GRCh38.p13 chr11: 66,946,001-67,700,500 , GRCh37.p13 chr11: 66,713,472-67,467,971 , PC, 38 more genes
    nsv4985091copy number variation1nstd200human GRCh38 chr11: 67,299,038-67,310,702 , GRCh37.p13 chr11: 67,066,509-67,078,173 SSH3, ANKRD13D
    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
    nsv4712776copy number variation1nstd195human GRCh37 chr11: 66,866,001-67,241,201 , GRCh38.p12 chr11: 67,098,530-67,473,730 PPP1CA, RPS6KB2, 19 more genes
    nsv4675137copy number variation1nstd102humanUncertain significance GRCh37 chr11: 66,820,585-67,979,510 , GRCh38.p12 chr11: 67,053,114-68,212,043 PPP1CA, RPS3AP40, 58 more genes
    nsv4618455copy number variation1nstd183human GRCh37 chr11: 67,025,374-67,084,761 , GRCh38.p12 chr11: 67,257,903-67,317,290 GRK2, KDM2A, 3 more genes
    nsv4349000copy number variation1nstd102humanPathogenic GRCh37 chr11: 65,138,976-67,574,402 , GRCh38.p12 chr11: 65,371,505-67,806,931 SNORD13F, ZNRD2, 141 more genes
    nsv4198337copy number variation1nstd166human GRCh37.p13 chr11: 67,079,175-67,079,299 , GRCh38.p12 chr11: 67,311,704-67,311,828 SSH3
    nsv3921639copy number variation1nstd102humanPathogenic NCBI36 chr11: 65,265,478-67,229,716 , GRCh37 chr11: 65,508,902-67,473,140 , GRCh38 chr11: 65,741,431-67,705,669 MIR6860, DOC2GP, 106 more genes
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