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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6131509insertion1nstd186human GRCh37 chr17: 36,628,620-36,628,670 , GRCh38.p12 chr17: 38,472,379-38,472,429 , GRCh38.p12 chr17|NT_187614.1: 2,507,686-2,507,736 ARHGAP23
    nsv6130051insertion1nstd186human GRCh37 chr17: 36,605,061-36,605,077 , GRCh38.p12 chr17: 38,448,817-38,448,833 , GRCh38.p12 chr17|NT_187614.1: 2,484,127-2,484,143 ARHGAP23, LOC101929494
    nsv5979095insertion1nstd209human GRCh38 chr17: 38,426,545-38,426,545 , GRCh37.p13 chr17: 36,582,792-36,582,792 ARHGAP23
    nsv5644923insertion1nstd207human GRCh38 chr17: 38,448,801-38,448,801 , GRCh37.p13 chr17: 36,605,045-36,605,045 LOC101929494, ARHGAP23
    nsv5594410copy number variation1nstd207human GRCh38 chr17: 38,500,010-38,500,152 , GRCh37.p13 chr17: 36,656,252-36,656,394 ARHGAP23
    nsv5589998copy number variation1nstd207human GRCh38 chr17: 38,482,695-38,485,042 , GRCh37.p13 chr17: 36,638,936-36,641,283 ARHGAP23
    nsv5585647copy number variation1nstd207human GRCh38 chr17: 38,505,852-38,516,369 , GRCh37.p13 chr17: 36,662,098-36,672,605 ARHGAP23
    nsv5563986sequence alteration1nstd206human GRCh38 chr17: 38,480,474-38,480,604 , GRCh37.p13 chr17: 36,636,715-36,636,845 ARHGAP23
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5551331insertion1nstd206human GRCh38 chr17: 38,448,817-38,448,833 , GRCh37.p13 chr17: 36,605,061-36,605,077 ARHGAP23, LOC101929494
    nsv5538009insertion1nstd206human GRCh38 chr17: 38,472,379-38,472,429 , GRCh37.p13 chr17: 36,628,620-36,628,670 ARHGAP23
    nsv5533877copy number variation1nstd206human GRCh38 chr17: 38,473,252-38,474,165 , GRCh37.p13 chr17: 36,629,493-36,630,406 ARHGAP23
    nsv5530129copy number variation1nstd206human GRCh38 chr17: 38,510,929-38,510,995 , GRCh37.p13 chr17: 36,667,165-36,667,231 ARHGAP23
    nsv5528417copy number variation1nstd206human GRCh38 chr17: 38,470,824-38,471,208 , GRCh37.p13 chr17: 36,627,065-36,627,449 ARHGAP23
    nsv5526261copy number variation1nstd206human GRCh38 chr17: 38,473,570-38,473,823 , GRCh37.p13 chr17: 36,629,811-36,630,064 ARHGAP23
    nsv5521239copy number variation1nstd206human GRCh38 chr17: 38,508,085-38,508,255 , GRCh37.p13 chr17: 36,664,331-36,664,501 ARHGAP23
    nsv5358842translocation1nstd200human GRCh38 chr17: 38,448,790-38,448,790 , GRCh38 chr17: 38,449,678-38,449,678 , GRCh37.p13 chr17: 36,605,034-36,605,034 , GRCh37.p13 chr17: 36,605,922-36,605,922 ARHGAP23, LOC101929494
    nsv5323581copy number variation1nstd204human GRCh38.p13 chr17: 38,422,345-38,422,447 , GRCh37.p13 chr17: 36,578,592-36,578,694 ARHGAP23
    nsv5149073mobile element insertion1nstd203human GRCh38 chr17: 38,480,595-38,480,644 , GRCh37.p13 chr17: 36,636,836-36,636,885 ARHGAP23
    nsv5148818mobile element insertion1nstd203human GRCh38 chr17: 38,448,801-38,448,817 , GRCh37.p13 chr17: 36,605,045-36,605,061 ARHGAP23, LOC101929494
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