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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094183copy number variation1nstd102humanUncertain significance GRCh37 chr11: 71,146,421-75,283,128 , GRCh38.p12 chr11: 71,435,375-75,572,083 LOC112268078, LRTOMT, 142 more genes
    nsv6915028copy number variation1nstd229human GRCh38 chr11: 72,076,848-72,080,558 , GRCh37.p13 chr11: 71,787,894-71,791,604 NUMA1, LRTOMT
    nsv6908275copy number variation1nstd229human GRCh38 chr11: 71,281,500-72,194,614 , GRCh37.p13 chr11: 71,088,949-71,905,658 DEFB130C, ANAPC15, 40 more genes
    nsv6905965copy number variation1nstd229human GRCh38 chr11: 72,068,712-72,078,794 , GRCh37.p13 chr11: 71,779,758-71,789,840 MIR3165, NUMA1, 1 more genes
    nsv6637545copy number variation1nstd102humanUncertain significance GRCh37 chr11: 71,777,538-72,144,933 , GRCh38.p12 chr11: 72,066,492-72,433,889 CLPB, FOLR3, 15 more genes
    nsv6470560copy number variation1nstd223human GRCh38 chr11: 72,025,209-72,302,197 , GRCh37.p13 chr11: 71,736,255-72,013,241 CLPB, FOLR3, 14 more genes
    nsv6467948copy number variation1nstd223human GRCh38 chr11: 72,070,769-72,084,018 , GRCh37.p13 chr11: 71,781,815-71,795,064 LRTOMT, NUMA1, 1 more genes
    nsv6465243copy number variation1nstd223human GRCh38 chr11: 72,068,712-72,078,792 , GRCh37.p13 chr11: 71,779,758-71,789,838 LRTOMT, MIR3165, 1 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
    nsv6314007copy number variation1nstd102humanUncertain significance GRCh37 chr11: 71,567,724-72,488,649 , GRCh38.p12 chr11: 71,856,678-72,777,604 STARD10, PDE2A, 38 more genes
    nsv6289694insertion1nstd214human GRCh38 chr11: 72,100,065-72,100,065 , GRCh37.p13 chr11: 71,811,111-71,811,111 LRTOMT, LAMTOR1
    nsv6248184mobile element insertion1nstd215human GRCh38 chr11: 72,101,854-72,101,854 , GRCh37.p13 chr11: 71,812,900-71,812,900 LAMTOR1, LRTOMT
    nsv6248183mobile element insertion1nstd215human GRCh38 chr11: 72,079,751-72,079,751 , GRCh37.p13 chr11: 71,790,797-71,790,797 NUMA1, LRTOMT
    nsv5927114copy number variation1nstd209human GRCh38 chr11: 72,098,858-72,099,109 , GRCh37.p13 chr11: 71,809,904-71,810,155 LRTOMT, LAMTOR1
    nsv5912882copy number variation1nstd209human GRCh38 chr11: 72,099,255-72,103,180 , GRCh37.p13 chr11: 71,810,301-71,814,226 LAMTOR1, LRTOMT
    nsv5911453copy number variation1nstd209human GRCh38 chr11: 72,109,926-72,110,084 , GRCh37.p13 chr11: 71,820,972-71,821,130 ANAPC15, LRTOMT
    nsv5911308copy number variation1nstd209human GRCh38 chr11: 72,098,415-72,098,779 , GRCh37.p13 chr11: 71,809,461-71,809,825 LRTOMT, LAMTOR1
    nsv5908624copy number variation1nstd209human GRCh38 chr11: 72,097,912-72,098,285 , GRCh37.p13 chr11: 71,808,958-71,809,331 LAMTOR1, LRTOMT
    nsv5511944copy number variation1nstd206human GRCh38 chr11: 72,098,418-72,098,733 , GRCh37.p13 chr11: 71,809,464-71,809,779 LAMTOR1, LRTOMT
    nsv5501878copy number variation1nstd206human GRCh38 chr11: 72,097,917-72,098,286 , GRCh37.p13 chr11: 71,808,963-71,809,332 LRTOMT, LAMTOR1
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