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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5964213insertion1nstd209human GRCh38 chr1: 78,118,884-78,118,884 , GRCh37.p13 chr1: 78,584,568-78,584,568 GIPC2
    nsv5884884copy number variation1nstd209human GRCh38 chr1: 78,061,615-78,061,730 , GRCh37.p13 chr1: 78,527,299-78,527,414 GIPC2
    nsv5877669copy number variation1nstd209human GRCh38 chr1: 78,099,283-78,099,342 , GRCh37.p13 chr1: 78,564,967-78,565,026 GIPC2
    nsv5869349copy number variation1nstd209human GRCh38 chr1: 78,098,660-78,099,906 , GRCh37.p13 chr1: 78,564,344-78,565,590 GIPC2
    nsv5830152copy number variation1nstd209human GRCh38 chr1: 78,098,687-78,099,923 , GRCh37.p13 chr1: 78,564,371-78,565,607 GIPC2
    nsv5726917mobile element insertion1nstd211human GRCh38 chr1: 78,090,711-78,090,711 , GRCh37.p13 chr1: 78,556,395-78,556,395 LOC100422537, GIPC2
    nsv5690170mobile element insertion2nstd211human GRCh38 chr1: 78,102,441-78,102,441 , GRCh37.p13 chr1: 78,568,125-78,568,125 GIPC2
    nsv5689949mobile element insertion1nstd211human GRCh38 chr1: 78,087,622-78,087,622 , GRCh37.p13 chr1: 78,553,306-78,553,306 RNU6-1102P, GIPC2
    nsv5688923mobile element insertion1nstd211human GRCh38 chr1: 78,133,715-78,133,715 , GRCh37.p13 chr1: 78,599,399-78,599,399 LOC107984997, GIPC2
    nsv5621374insertion1nstd207human GRCh38 chr1: 78,102,427-78,102,427 , GRCh37.p13 chr1: 78,568,111-78,568,111 GIPC2
    nsv5581743copy number variation1nstd207human GRCh38 chr1: 78,061,615-78,061,730 , GRCh37.p13 chr1: 78,527,299-78,527,414 GIPC2
    nsv5555331mobile element insertion1nstd206human GRCh38 chr1: 78,090,726-78,090,749 , GRCh37.p13 chr1: 78,556,410-78,556,433 GIPC2, LOC100422537
    nsv5427072copy number variation1nstd206human GRCh38 chr1: 78,130,162-78,131,207 , GRCh37.p13 chr1: 78,595,846-78,596,891 LOC107984997, GIPC2
    nsv5421217copy number variation1nstd206human GRCh38 chr1: 78,077,835-78,087,417 , GRCh37.p13 chr1: 78,543,519-78,553,101 RNU6-1102P, GIPC2
    nsv5417296copy number variation1nstd206human GRCh38 chr1: 78,061,637-78,061,712 , GRCh37.p13 chr1: 78,527,321-78,527,396 GIPC2
    nsv5416912copy number variation1nstd206human GRCh38 chr1: 78,098,661-78,099,907 , GRCh37.p13 chr1: 78,564,345-78,565,591 GIPC2
    nsv5403387mobile element insertion1nstd206human GRCh38 chr1: 78,087,572-78,087,622 , GRCh37.p13 chr1: 78,553,256-78,553,306 GIPC2, RNU6-1102P
    nsv5347095translocation1nstd200human GRCh38 chr1: 78,098,661-78,098,661 , GRCh38 chr1: 78,099,907-78,099,907 , GRCh37.p13 chr1: 78,564,345-78,564,345 , GRCh37.p13 chr1: 78,565,591-78,565,591 GIPC2
    nsv5340477translocation1nstd200human GRCh37 chr1: 78,564,345-78,564,345 , GRCh37 chr1: 78,565,591-78,565,591 , GRCh38.p12 chr1: 78,098,661-78,098,661 , GRCh38.p12 chr1: 78,099,907-78,099,907 GIPC2
    nsv5294346copy number variation1nstd204human GRCh38.p13 chr1: 78,061,637-78,061,712 , GRCh37.p13 chr1: 78,527,321-78,527,396 GIPC2
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