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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
    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
    nsv6911196copy number variation1nstd229human GRCh38 chr11: 66,960,891-66,996,689 , GRCh37.p13 chr11: 66,728,362-66,764,160 C11orf86
    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
    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
    nsv6313974copy number variation1nstd102humanUncertain significance GRCh37 chr11: 66,673,078-66,942,028 , GRCh38.p12 chr11: 66,905,607-67,174,557 RHOD, MIR6860, 7 more genes
    nsv6248158mobile element insertion1nstd215human GRCh38 chr11: 66,974,298-66,974,298 , GRCh37.p13 chr11: 66,741,769-66,741,769 C11orf86
    nsv6132114copy number variation1nstd213human GRCh37 chr11: 66,670,000-66,970,001 , GRCh38.p12 chr11: 66,902,529-67,202,530 PC, KDM2A, 7 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
    nsv6037635copy number variation1nstd212human GRCh38 chr11: 66,973,455-66,973,631 , GRCh37.p13 chr11: 66,740,926-66,741,102 C11orf86
    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
    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
    nsv4375610copy number variation1nstd173human GRCh37 chr11: 66,673,079-66,760,870 , GRCh38.p12 chr11: 66,905,608-66,993,399 , MIR3163, 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
    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
    nsv3917536copy number variation1nstd102humanPathogenic NCBI36 chr11: 66,409,957-67,222,297 , GRCh38 chr11: 66,885,910-67,698,250 , GRCh37 chr11: 66,653,381-67,465,721 PPP1CA, TBC1D10C, 39 more genes
    nsv3911732copy number variation1nstd102humanPathogenic GRCh38 chr11: 66,193,502-67,890,770 , GRCh37 chr11: 65,960,973-67,658,241 , NCBI36 chr11: 65,717,549-67,414,817 B4GAT1, KDM2A, 90 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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