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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093694copy number variation2nstd102humanUncertain significance GRCh37 chr11: 58,916,346-64,972,349 , GRCh38.p12 chr11: 59,148,873-65,204,878 VPS37C, POLR2G, 298 more genes
    nsv6913010copy number variation1nstd229human GRCh38 chr11: 64,818,948-64,869,199 , GRCh37.p13 chr11: 64,586,420-64,636,671 EHD1, CDC42BPG
    nsv6912005copy number variation1nstd229human GRCh38 chr11: 64,878,684-64,901,793 , GRCh37.p13 chr11: 64,646,156-64,669,265 MIR6750, EHD1, 7 more genes
    nsv6909375copy number variation1nstd229human GRCh38 chr11: 64,858,994-64,859,141 , GRCh37.p13 chr11: 64,626,466-64,626,613 EHD1
    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
    nsv6903095copy number variation1nstd229human GRCh38 chr11: 59,466,654-66,168,743 , GRCh37.p13 chr11: 59,234,127-65,936,214 LINC02724, TMEM132A, 342 more genes
    nsv6900539copy number variation1nstd229human GRCh38 chr11: 64,846,703-64,852,392 , GRCh37.p13 chr11: 64,614,175-64,619,864 EHD1
    nsv6470306copy number variation1nstd223human GRCh38 chr11: 64,867,530-64,886,506 , GRCh37.p13 chr11: 64,635,002-64,653,978 MIR194-2HG, EHD1, 2 more genes
    nsv6467972copy number variation1nstd223human GRCh38 chr11: 64,845,523-64,919,247 , GRCh37.p13 chr11: 64,612,995-64,686,719 RPS16P6, MIR194-2, 8 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
    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
    nsv6203467copy number variation1nstd214human GRCh38 chr11: 64,855,962-64,856,022 , GRCh37.p13 chr11: 64,623,434-64,623,494 EHD1
    nsv6201910copy number variation1nstd214human GRCh38 chr11: 64,855,905-64,855,998 , GRCh37.p13 chr11: 64,623,377-64,623,470 EHD1
    nsv6196126copy number variation1nstd214human GRCh38 chr11: 64,855,856-64,855,951 , GRCh37.p13 chr11: 64,623,328-64,623,423 EHD1
    nsv6195497copy number variation1nstd214human GRCh38 chr11: 64,855,889-64,855,980 , GRCh37.p13 chr11: 64,623,361-64,623,452 EHD1
    nsv6193967copy number variation1nstd214human GRCh38 chr11: 64,855,839-64,855,934 , GRCh37.p13 chr11: 64,623,311-64,623,406 EHD1
    nsv6193627copy number variation1nstd214human GRCh38 chr11: 64,855,856-64,855,919 , GRCh37.p13 chr11: 64,623,328-64,623,391 EHD1
    nsv6190919copy number variation1nstd214human GRCh38 chr11: 64,855,889-64,855,981 , GRCh37.p13 chr11: 64,623,361-64,623,453 EHD1
    nsv6188862copy number variation1nstd214human GRCh38 chr11: 64,855,906-64,856,026 , GRCh37.p13 chr11: 64,623,378-64,623,498 EHD1
    nsv6132269copy number variation1nstd213human GRCh37 chr11: 64,390,000-65,950,001 , GRCh38.p12 chr11: 64,622,528-66,182,530 MRPL49, CTSW, 103 more genes
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