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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093669copy number variation2nstd102humanUncertain significance GRCh37 chr11: 111,171,709-112,104,278 , GRCh38.p12 chr11: 111,300,984-112,233,555 CRYAB, RPS6P16, 43 more genes
    nsv7074145inversion1nstd229human GRCh38 chr11: 104,112,094-113,544,164 , GRCh37.p13 chr11: 103,982,822-113,414,886 COLCA1, LOC105369491, 150 more genes
    nsv7069281inversion1nstd229human GRCh38 chr11: 107,936,485-114,400,629 , GRCh37.p13 chr11: 107,807,211-114,271,351 LRRC37A13P, POU2AF3, 121 more genes
    nsv7065935inversion1nstd229human GRCh38 chr11: 107,044,115-113,544,291 , GRCh37.p13 chr11: 106,914,841-113,415,013 LINC02762, TIMM8B, 112 more genes
    nsv6915249copy number variation1nstd229human GRCh38 chr11: 112,198,427-112,225,388 , GRCh37.p13 chr11: 112,069,150-112,096,111 BCO2, MRPS36P4, 2 more genes
    nsv6912662copy number variation1nstd229human GRCh38 chr11: 112,174,947-112,213,945 , GRCh37.p13 chr11: 112,045,670-112,084,668 MRPS36P4, KCTD9P4, 1 more genes
    nsv6900237copy number variation1nstd229human GRCh38 chr11: 112,196,001-112,247,900 , GRCh37.p13 chr11: 112,066,724-112,118,623 RPS12P21, PTS, 4 more genes
    nsv6637811copy number variation1nstd102humanPathogenic GRCh37 chr11: 109,328,787-116,414,966 , GRCh38.p12 chr11: 109,458,061-116,544,249 LOC102723966, NXPE4, 129 more genes
    nsv6620697copy number variation1nstd224human GRCh37 chr11: 112,064,216-112,362,462 , GRCh38.p12 chr11: 112,193,493-112,491,739 MRPS36P4, PLET1, 12 more genes
    nsv6620696copy number variation2nstd224human GRCh37 chr11: 112,050,025-112,084,583 , GRCh38.p12 chr11: 112,179,302-112,213,860 BCO2, MRPS36P4, 1 more genes
    nsv6620695copy number variation1nstd224human GRCh37 chr11: 111,953,288-112,208,967 , GRCh38.p12 chr11: 112,082,564-112,338,244 TIMM8B, NKAPD1, 15 more genes
    nsv6588870inversion1nstd223human GRCh38 chr11: 112,214,164-112,215,520 , GRCh37.p13 chr11: 112,084,887-112,086,243 BCO2
    nsv6586799inversion1nstd223human GRCh38 chr11: 112,202,286-112,203,062 , GRCh37.p13 chr11: 112,073,009-112,073,785 BCO2
    nsv6586218inversion1nstd223human GRCh38 chr11: 107,936,497-114,408,912 , GRCh37.p13 chr11: 107,807,223-114,279,634 LOC107984390, ATF4P4, 121 more genes
    nsv6584567inversion1nstd223human GRCh38 chr11: 112,206,055-112,206,121 , GRCh37.p13 chr11: 112,076,778-112,076,844 BCO2
    nsv6474741copy number variation1nstd223human GRCh38 chr11: 112,201,101-112,236,800 , GRCh37.p13 chr11: 112,071,824-112,107,523 RPS6P16, PTS, 3 more genes
    nsv6470939copy number variation1nstd223human GRCh38 chr11: 112,174,947-112,213,940 , GRCh37.p13 chr11: 112,045,670-112,084,663 MRPS36P4, BCO2, 1 more genes
    nsv6467449copy number variation1nstd223human GRCh38 chr11: 112,202,301-112,208,400 , GRCh37.p13 chr11: 112,073,024-112,079,123 BCO2, MRPS36P4
    nsv6460916copy number variation1nstd223human GRCh38 chr11: 112,173,969-112,175,251 , GRCh37.p13 chr11: 112,044,692-112,045,974 BCO2
    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
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