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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148271copy number variation1nstd102humanPathogenic GRCh38 chr18: 158,286-14,124,574 , GRCh37.p13 chr18: 158,286-14,124,573 PMM2P2, EIF4A2P1, 225 more genes
    nsv7143197insertion1nstd232human GRCh37.p13 chr18: 12,851,196-12,851,196 , GRCh38.p12 chr18: 12,851,197-12,851,197 PTPN2
    nsv7098917copy number variation1nstd102humanPathogenic GRCh37 chr18: 1-15,400,035 , GRCh38.p12 chr18: 10,001-15,400,036 RNU7-25P, RPL6P27, 275 more genes
    nsv7077914inversion1nstd229human GRCh38 chr18: 12,802,446-12,918,549 , GRCh37.p13 chr18: 12,802,445-12,918,548 PTPN2, STK25P1, 1 more genes
    nsv7074186inversion1nstd229human GRCh38 chr18: 7,953,048-15,343,982 , GRCh37.p13 chr18: 7,953,046-15,343,981 PSMG2, EIF4A2P1, 155 more genes
    nsv7071462inversion1nstd229human GRCh38 chr18: 12,879,378-12,879,400 , GRCh37.p13 chr18: 12,879,377-12,879,399 PTPN2
    nsv7068092inversion1nstd229human GRCh38 chr18: 12,777,192-12,907,087 , GRCh37.p13 chr18: 12,777,191-12,907,086 PTPN2
    nsv7059812inversion1nstd229human GRCh38 chr18: 12,801,924-12,802,006 , GRCh37.p13 chr18: 12,801,923-12,802,005 PTPN2
    nsv7015576copy number variation1nstd229human GRCh38 chr18: 12,816,941-12,817,146 , GRCh37.p13 chr18: 12,816,940-12,817,145 PTPN2
    nsv7015128copy number variation1nstd229human GRCh38 chr18: 4,434,377-14,413,632 , GRCh37.p13 chr18: 4,434,377-14,413,631 RAB31, THEMIS3P, 167 more genes
    nsv7013652copy number variation1nstd229human GRCh38 chr18: 12,851,183-12,851,512 , GRCh37.p13 chr18: 12,851,182-12,851,511 PTPN2
    nsv7013259copy number variation1nstd229human GRCh38 chr18: 12,873,301-12,899,100 , GRCh37.p13 chr18: 12,873,300-12,899,099 PTPN2
    nsv7012063copy number variation1nstd229human GRCh38 chr18: 12,719,130-12,784,114 , GRCh37.p13 chr18: 12,719,129-12,784,113 LINC01882, PSMG2, 1 more genes
    nsv7010751copy number variation1nstd229human GRCh38 chr18: 12,884,321-12,900,620 , GRCh37.p13 chr18: 12,884,320-12,900,619 PTPN2
    nsv7010603copy number variation1nstd229human GRCh38 chr18: 12,597,906-12,834,055 , GRCh37.p13 chr18: 12,597,905-12,834,054 LINC01882, CEP76, 3 more genes
    nsv7009793copy number variation1nstd229human GRCh38 chr18: 12,842,192-12,850,925 , GRCh37.p13 chr18: 12,842,191-12,850,924 PTPN2
    nsv7009756copy number variation1nstd229human GRCh38 chr18: 12,483,561-12,800,777 , GRCh37.p13 chr18: 12,483,560-12,800,776 CEP76, PTPN2, 3 more genes
    nsv7008534copy number variation1nstd229human GRCh38 chr18: 12,859,701-13,003,700 , GRCh37.p13 chr18: 12,859,700-13,003,699 PTPN2, STK25P1, 3 more genes
    nsv7007338copy number variation1nstd229human GRCh38 chr18: 12,805,501-12,811,500 , GRCh37.p13 chr18: 12,805,500-12,811,499 PTPN2
    nsv7007127copy number variation1nstd229human GRCh38 chr18: 12,791,715-12,791,877 , GRCh37.p13 chr18: 12,791,714-12,791,876 PTPN2
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