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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094096copy number variation1nstd102humanUncertain significance GRCh37 chr11: 66,099,747-66,291,373 , GRCh38.p12 chr11: 66,332,276-66,523,902 LOC100505524, BRMS1, 14 more genes
    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
    nsv7093406copy number variation1nstd102humanUncertain significance GRCh37 chr11: 66,178,392-66,433,436 , GRCh38.p12 chr11: 66,410,921-66,665,965 MRPL11, NPAS4, 15 more genes
    nsv6917745copy number variation1nstd229human GRCh38 chr11: 66,467,997-66,468,247 , GRCh37.p13 chr11: 66,235,468-66,235,718 PELI3
    nsv6909531copy number variation1nstd229human GRCh38 chr11: 66,461,921-66,467,689 , GRCh37.p13 chr11: 66,229,392-66,235,160 PELI3
    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
    nsv6314192copy number variation1nstd102humanUncertain significance GRCh37 chr11: 64,935,724-66,405,514 , GRCh38.p12 chr11: 65,168,253-66,638,043 CNIH2, GAL3ST3, 95 more genes
    nsv6314012copy number variation1nstd102humanUncertain significance GRCh37 chr11: 66,188,172-66,402,747 , GRCh38.p12 chr11: 66,420,701-66,635,276 LOC100505524, ZDHHC24, 13 more genes
    nsv6309121copy number variation2nstd102humanPathogenic GRCh37 chr11: 64,522,783-66,283,694 , GRCh38.p12 chr11: 64,755,311-66,516,223 SF3B2, ZNRD2-DT, 124 more genes
    nsv6290938copy number variation1nstd102humanUncertain significance GRCh37 chr11: 65,963,737-66,581,485 , GRCh38.p12 chr11: 66,196,266-66,814,014 CCS, RN7SL12P, 38 more genes
    nsv6132271copy number variation1nstd213human GRCh37 chr11: 66,040,000-66,380,001 , GRCh38.p12 chr11: 66,272,529-66,612,530 BBS1, YIF1A, 24 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
    nsv5510688copy number variation1nstd206human GRCh38 chr11: 66,467,997-66,468,250 , GRCh37.p13 chr11: 66,235,468-66,235,721 PELI3
    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
    nsv5277798copy number variation1nstd204human GRCh38.p13 chr11: 65,676,501-66,823,500 , GRCh37.p13 chr11: 65,443,972-66,590,971 , BBS1, 68 more genes
    nsv5262105copy number variation1nstd204human GRCh38.p13 chr11: 66,460,101-66,518,100 , GRCh37.p13 chr11: 66,227,572-66,285,571 DPP3-DT, DPP3, 2 more genes
    nsv4979889copy number variation1nstd200human GRCh38 chr11: 66,461,920-66,467,688 , GRCh37.p13 chr11: 66,229,391-66,235,159 PELI3
    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
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