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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5856622copy number variation2nstd209human GRCh38 chr11: 68,872,465-68,874,453 , GRCh37.p13 chr11: 68,639,933-68,641,921 LINC02701
    nsv5854630copy number variation3nstd209human GRCh38 chr11: 68,867,543-68,873,864 , GRCh37.p13 chr11: 68,635,011-68,641,332 LINC02701
    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
    nsv4980006copy number variation1nstd200human GRCh38 chr11: 68,850,663-68,884,152 , GRCh37.p13 chr11: 68,618,131-68,651,620 LINC02701
    nsv4845099copy number variation1nstd200human GRCh37 chr11: 68,624,690-68,652,772 , GRCh38.p12 chr11: 68,857,222-68,885,304 LINC02701
    nsv4830229copy number variation1nstd200human GRCh37 chr11: 68,618,131-68,651,620 , GRCh38.p12 chr11: 68,850,663-68,884,152 LINC02701
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4715326copy number variation1nstd195human GRCh37 chr11: 68,355,451-69,089,801 , GRCh38.p12 chr11: 68,587,983-69,322,333 , CPT1A, 19 more genes
    nsv4712792copy number variation1nstd195human GRCh37 chr11: 68,629,801-69,089,801 , GRCh38.p12 chr11: 68,862,333-69,322,333 , LOC338694, 14 more genes
    nsv4528829copy number variation1nstd166human GRCh37.p13 chr11: 68,635,000-68,642,000 , GRCh38.p12 chr11: 68,867,532-68,874,532 LINC02701
    nsv4528628copy number variation1nstd166human GRCh37.p13 chr11: 68,306,151-68,837,546 , GRCh38.p12 chr11: 68,538,683-69,070,078 GAL, LOC107984343, 10 more genes
    nsv3960703insertion1nstd168human GRCh38 chr11: 68,844,030-68,898,521 , GRCh37.p13 chr11: 68,611,498-68,665,989 CPT1A, MRPL21, 1 more genes
    nsv3920906copy number variation1nstd102humanLikely pathogenic NCBI36 chr11: 66,741,311-68,972,547 , GRCh37 chr11: 66,984,735-69,263,366 , GRCh38 chr11: 67,217,264-69,448,598 GRK2, ALDH3B1, 82 more genes
    nsv3917463copy number variation1nstd102humanLikely pathogenic NCBI36 chr11: 67,555,736-70,982,189 , GRCh37 chr11: 67,799,160-71,304,541 , GRCh38 chr11: 68,031,693-71,593,495 CCND1, CHKA, 71 more genes
    nsv3914930copy number variation1nstd102humanLikely benign GRCh37 chr11: 67,973,430-69,395,243 , GRCh38 chr11: 68,205,963-69,580,475 , NCBI36 chr11: 67,730,006-69,104,424 LINC02747, LOC105369366, 27 more genes
    nsv3909768copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 67,799,160-70,701,268 , GRCh38.p12 chr11: 68,031,693-70,855,163 CCND1, CHKA, 56 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
    nsv3900144copy number variation1nstd102humanPathogenic GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169 RTN3, KRTAP5-13P, 2833 more genes
    nsv3893233copy number variation1nstd102humanPathogenic GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576 LOC105376598, OSBPL9P2, 2842 more genes
    nsv3155956copy number variation1nstd151human GRCh37 chr11: 68,512,456-68,658,868 , GRCh38.p12 chr11: 68,744,988-68,891,400 TESMIN, MRPL21, 2 more genes
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