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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5932186copy number variation1nstd209human GRCh38 chr13: 77,934,881-83,910,012 , GRCh37.p13 chr13: 78,509,016-84,484,147 NDFIP2, LINC01068, 54 more genes
    nsv5694691mobile element insertion2nstd211human GRCh38 chr13: 79,895,819-79,895,819 , GRCh37.p13 chr13: 80,469,954-80,469,954 LINC00382
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 RN7SL272P, DIAPH3, 1333 more genes
    nsv5501343copy number variation1nstd206human GRCh38 chr13: 79,880,767-79,886,003 , GRCh37.p13 chr13: 80,454,902-80,460,138 LINC00382
    nsv5414485mobile element insertion1nstd206human GRCh38 chr13: 79,895,819-79,895,870 , GRCh37.p13 chr13: 80,469,954-80,470,005 LINC00382
    nsv5348744translocation1nstd200human GRCh38 chr13: 79,880,767-79,880,767 , GRCh38 chr13: 79,886,003-79,886,003 , GRCh37.p13 chr13: 80,460,138-80,460,138 , GRCh37.p13 chr13: 80,454,902-80,454,902 LINC00382
    nsv5303402copy number variation1nstd204human GRCh38.p13 chr13: 79,880,766-79,886,003 , GRCh37.p13 chr13: 80,454,901-80,460,138 LINC00382
    nsv5277325copy number variation1nstd204human GRCh38.p13 chr13: 79,880,595-79,886,021 , GRCh37.p13 chr13: 80,454,730-80,460,156 LINC00382
    nsv5261143copy number variation1nstd204human GRCh38.p13 chr13: 79,884,401-79,886,000 , GRCh37.p13 chr13: 80,458,536-80,460,135 LINC00382
    nsv5033445inversion1nstd200human GRCh38 chr13: 63,639,797-112,722,344 , GRCh37.p13 chr13: 64,213,930-113,376,658 , RPL15P18, 564 more genes
    nsv5008890copy number variation1nstd200human GRCh38 chr13: 79,891,566-79,892,918 , GRCh37.p13 chr13: 80,465,701-80,467,053 LINC00382
    nsv4871044inversion1nstd200human GRCh37 chr13: 64,213,930-113,376,658 , GRCh38.p12 chr13: 63,639,797-112,722,344 , TUBGCP3, 564 more genes
    nsv4848366copy number variation1nstd200human GRCh37 chr13: 80,270,140-80,520,410 , GRCh38.p12 chr13: 79,696,005-79,946,275 LINC01038, LINC00382
    nsv4835262copy number variation1nstd200human GRCh37 chr13: 80,454,902-80,460,138 , GRCh38.p12 chr13: 79,880,767-79,886,003 LINC00382
    nsv4675995copy number variation1nstd102humanPathogenic GRCh37 chr13: 51,512,603-91,631,111 , GRCh38.p12 chr13: 50,938,467-90,978,857 RNU7-88P, LINC00564, 396 more genes
    nsv4675850copy number variation1nstd102humanPathogenic GRCh37 chr13: 53,262,013-115,107,733 , GRCh38.p12 chr13: 52,687,878-114,342,258 TEX30, LOC101927712, 680 more genes
    nsv4675244copy number variation1nstd102humanPathogenic GRCh37 chr13: 71,502,357-86,571,730 , GRCh38.p12 chr13: 70,928,225-85,997,595 RNU6-79P, LINC01069, 151 more genes
    nsv4614603copy number variation1nstd183human GRCh37 chr13: 80,419,508-80,457,698 , GRCh38.p12 chr13: 79,845,373-79,883,563 LINC00382
    nsv4610841copy number variation1nstd183human GRCh37 chr13: 80,476,614-80,618,826 , GRCh38.p12 chr13: 79,902,479-80,044,691 LINC01080, LINC00382
    nsv4605232copy number variation1nstd183human GRCh37 chr13: 80,454,900-80,460,138 , GRCh38.p12 chr13: 79,880,765-79,886,003 LINC00382
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