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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144246insertion1nstd232human GRCh37.p13 chr18: 19,379,937-19,379,937 , GRCh38.p12 chr18: 21,799,976-21,799,976 MIB1
    nsv7142693insertion1nstd232human GRCh37.p13 chr18: 19,383,977-19,383,977 , GRCh38.p12 chr18: 21,804,016-21,804,016 MIB1
    nsv7138334insertion1nstd232human GRCh37.p13 chr18: 19,399,607-19,399,607 , GRCh38.p12 chr18: 21,819,646-21,819,646 MIB1
    nsv7095431copy number variation1nstd102humanUncertain significance GRCh37 chr18: 18,963,480-21,534,612 , GRCh38.p12 chr18: 21,383,519-23,954,648 MIB1, RN7SL233P, 41 more genes
    nsv7095001copy number variation1nstd102humanUncertain significance GRCh37 chr18: 19,383,858-19,780,786 , GRCh38.p12 chr18: 21,803,897-22,200,823 MIR1-2, LINC01900, 12 more genes
    nsv7073318inversion1nstd229human GRCh38 chr18: 21,866,113-23,515,547 , GRCh37.p13 chr18: 19,446,074-21,095,511 RNA5SP451, GATA6, 26 more genes
    nsv7069112inversion1nstd229human GRCh38 chr18: 21,862,475-21,868,594 , GRCh37.p13 chr18: 19,442,436-19,448,555 MIB1
    nsv7017561copy number variation1nstd229human GRCh38 chr18: 21,747,882-21,753,493 , GRCh37.p13 chr18: 19,327,843-19,333,454 MIB1
    nsv7014915copy number variation1nstd229human GRCh38 chr18: 21,782,477-21,783,889 , GRCh37.p13 chr18: 19,362,438-19,363,850 MIB1
    nsv7014775copy number variation1nstd229human GRCh38 chr18: 21,751,201-21,761,100 , GRCh37.p13 chr18: 19,331,162-19,341,061 MIB1
    nsv7013900copy number variation1nstd229human GRCh38 chr18: 21,782,312-21,783,397 , GRCh37.p13 chr18: 19,362,273-19,363,358 MIB1
    nsv7012744copy number variation1nstd229human GRCh38 chr18: 21,783,176-21,787,982 , GRCh37.p13 chr18: 19,363,137-19,367,943 MIB1
    nsv7011731copy number variation1nstd229human GRCh38 chr18: 21,746,305-21,749,936 , GRCh37.p13 chr18: 19,326,266-19,329,897 MIB1
    nsv7009330copy number variation1nstd229human GRCh38 chr18: 21,755,501-21,757,700 , GRCh37.p13 chr18: 19,335,462-19,337,661 MIB1
    nsv7009229copy number variation1nstd229human GRCh38 chr18: 21,759,133-21,759,679 , GRCh37.p13 chr18: 19,339,094-19,339,640 MIB1
    nsv7009190copy number variation1nstd229human GRCh38 chr18: 21,855,101-21,858,800 , GRCh37.p13 chr18: 19,435,062-19,438,761 RPL34P32, MIB1
    nsv7008765copy number variation1nstd229human GRCh38 chr18: 21,781,616-21,783,445 , GRCh37.p13 chr18: 19,361,577-19,363,406 MIB1
    nsv7006888copy number variation1nstd229human GRCh38 chr18: 21,843,801-21,849,400 , GRCh37.p13 chr18: 19,423,762-19,429,361 MIB1
    nsv7005906copy number variation1nstd229human GRCh38 chr18: 21,792,727-21,792,909 , GRCh37.p13 chr18: 19,372,688-19,372,870 MIB1, RN7SL233P
    nsv7004465copy number variation1nstd229human GRCh38 chr18: 21,820,701-21,823,600 , GRCh37.p13 chr18: 19,400,662-19,403,561 MIB1, MIR133A1HG
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