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Items: 1 to 20 of 108

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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
    nsv6908485copy number variation1nstd229human GRCh38 chr11: 66,371,501-66,372,200 , GRCh37.p13 chr11: 66,138,972-66,139,671 SLC29A2
    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
    nsv6900451copy number variation1nstd229human GRCh38 chr11: 66,365,632-66,373,097 , GRCh37.p13 chr11: 66,133,103-66,140,568 SLC29A2
    nsv6474430copy number variation1nstd223human GRCh38 chr11: 66,365,632-66,373,092 , GRCh37.p13 chr11: 66,133,103-66,140,563 SLC29A2
    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
    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
    nsv6302270copy number variation1nstd186human GRCh37 chr11: 66,131,486-66,131,536 , GRCh38.p12 chr11: 66,364,015-66,364,065 SLC29A2, B4GAT1-DT
    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
    nsv5510045copy number variation1nstd206human GRCh38 chr11: 66,365,632-66,373,092 , GRCh37.p13 chr11: 66,133,103-66,140,563 SLC29A2
    nsv5498287copy number variation1nstd206human GRCh38 chr11: 66,364,015-66,364,065 , GRCh37.p13 chr11: 66,131,486-66,131,536 B4GAT1-DT, SLC29A2
    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
    nsv4979884copy number variation1nstd200human GRCh38 chr11: 66,365,632-66,373,092 , GRCh37.p13 chr11: 66,133,103-66,140,563 SLC29A2
    nsv4835601copy number variation1nstd200human GRCh37 chr11: 66,133,103-66,140,563 , GRCh38.p12 chr11: 66,365,632-66,373,092 SLC29A2
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
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