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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137096copy number variation1nstd102humanLikely benign GRCh37 chr11: 5,094,756-5,785,959 , GRCh38.p12 chr11: 5,073,526-5,764,729 OR51J1, OLFM5P, 52 more genes
    nsv6917621copy number variation1nstd229human GRCh38 chr11: 5,602,366-5,602,878 , GRCh37.p13 chr11: 5,623,596-5,624,108 TRIM5, TRIM6, 1 more genes
    nsv6917011copy number variation1nstd229human GRCh38 chr11: 2,693,282-9,207,515 , GRCh37.p13 chr11: 2,714,512-9,229,062 LOC105376526, OR51E2, 279 more genes
    nsv6912665copy number variation1nstd229human GRCh38 chr11: 5,615,647-5,615,947 , GRCh37.p13 chr11: 5,636,877-5,637,177 TRIM5, TRIM6-TRIM34
    nsv6912031copy number variation1nstd229human GRCh38 chr11: 5,583,774-5,599,656 , GRCh37.p13 chr11: 5,605,004-5,620,886 TRIM6, TRIM5, 1 more genes
    nsv6905928copy number variation1nstd229human GRCh38 chr11: 5,562,900-5,620,666 , GRCh37.p13 chr11: 5,584,130-5,641,896 OR52B6, OR52T1P, 5 more genes
    nsv6905315copy number variation1nstd229human GRCh38 chr11: 5,602,185-5,602,673 , GRCh37.p13 chr11: 5,623,415-5,623,903 TRIM5, TRIM6-TRIM34, 1 more genes
    nsv6904825copy number variation1nstd229human GRCh38 chr11: 5,612,053-5,635,160 , GRCh37.p13 chr11: 5,633,283-5,656,390 TRIM34, TRIM6-TRIM34, 2 more genes
    nsv6902633copy number variation1nstd229human GRCh38 chr11: 5,538,086-5,938,396 , GRCh37.p13 chr11: 5,559,316-5,959,626 OR52N1, OR52N4, 26 more genes
    nsv6901531copy number variation1nstd229human GRCh38 chr11: 5,596,401-5,596,424 , GRCh37.p13 chr11: 5,617,631-5,617,654 TRIM5, TRIM6-TRIM34, 1 more genes
    nsv6898989copy number variation1nstd229human GRCh38 chr11: 5,583,815-5,622,509 , GRCh37.p13 chr11: 5,605,045-5,643,739 TRIM6-TRIM34, TRIM34, 2 more genes
    nsv6898769copy number variation1nstd229human GRCh38 chr11: 5,442,003-5,689,638 , GRCh37.p13 chr11: 5,463,233-5,710,868 TRIM6, TRIM22, 19 more genes
    nsv6898523copy number variation1nstd229human GRCh38 chr11: 5,627,235-5,637,002 , GRCh37.p13 chr11: 5,648,465-5,658,232 TRIM34, TRIM6-TRIM34, 1 more genes
    nsv6638042copy number variation1nstd102humanUncertain significance GRCh37 chr11: 5,361,272-5,660,023 , GRCh38.p12 chr11: 5,340,042-5,638,793 OR51A10P, OR52H2P, 24 more genes
    nsv6637864copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,616-8,250,724 , GRCh38.p12 chr11: 230,616-8,229,177 PNPLA2, OR52H1, 372 more genes
    nsv6637234copy number variation1nstd102humanUncertain significance GRCh37 chr11: 5,279,153-5,619,949 , GRCh38.p12 chr11: 5,257,923-5,598,719 OR51A10P, OR51B5, 29 more genes
    nsv6621003copy number variation1nstd224human GRCh37 chr11: 5,633,747-5,655,976 , GRCh38.p12 chr11: 5,612,517-5,634,746 TRIM5, TRIM34, 2 more genes
    nsv6582867inversion1nstd223human GRCh38 chr11: 5,629,153-5,629,817 , GRCh37.p13 chr11: 5,650,383-5,651,047 TRIM34, TRIM5, 1 more genes
    nsv6454240copy number variation1nstd223human GRCh38 chr11: 5,583,762-5,599,625 , GRCh37.p13 chr11: 5,604,992-5,620,855 TRIM6-TRIM34, TRIM6, 1 more genes
    nsv6441849copy number variation1nstd223human GRCh38 chr11: 5,588,812-6,011,442 , GRCh37.p13 chr11: 5,610,042-6,032,672 OR52N5, OR52N4, 26 more genes
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