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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
    nsv7098917copy number variation1nstd102humanPathogenic GRCh37 chr18: 1-15,400,035 , GRCh38.p12 chr18: 10,001-15,400,036 RNU7-25P, RPL6P27, 275 more genes
    nsv7095258copy number variation1nstd102humanUncertain significance GRCh37 chr18: 9,102,742-12,725,530 , GRCh38.p12 chr18: 9,102,744-12,725,531 PIEZO2, RALBP1, 77 more genes
    nsv7074238inversion1nstd229human GRCh38 chr18: 11,064,740-12,270,817 , GRCh37.p13 chr18: 11,064,739-12,270,816 MIX23P3, PMM2P2, 26 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
    nsv7074061inversion1nstd229human GRCh38 chr18: 10,416,984-12,233,354 , GRCh37.p13 chr18: 10,416,981-12,233,353 LOC107985173, PIEZO2, 34 more genes
    nsv7061706inversion1nstd229human GRCh38 chr18: 10,611,512-12,224,186 , GRCh37.p13 chr18: 10,611,509-12,224,185 C18orf61, LOC100533852, 31 more genes
    nsv7059396inversion1nstd229human GRCh38 chr18: 10,628,787-12,219,101 , GRCh37.p13 chr18: 10,628,784-12,219,100 LOC100533852, MPPE1, 29 more genes
    nsv7016176copy number variation1nstd229human GRCh38 chr18: 12,213,494-12,216,573 , GRCh37.p13 chr18: 12,213,493-12,216,572 C18orf61
    nsv7016047copy number variation1nstd229human GRCh38 chr18: 12,188,202-12,333,162 , GRCh37.p13 chr18: 12,188,201-12,333,161 C18orf61, AFG3L2, 6 more genes
    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
    nsv7012784copy number variation1nstd229human GRCh38 chr18: 12,146,492-12,285,342 , GRCh37.p13 chr18: 12,146,491-12,285,341 CIDEA, C18orf61, 4 more genes
    nsv7003207copy number variation1nstd229human GRCh38 chr18: 11,244,551-12,953,481 , GRCh37.p13 chr18: 11,244,550-12,953,480 LINC01255, AFG3L2, 41 more genes
    nsv6999801copy number variation1nstd229human GRCh38 chr18: 12,000,674-12,871,099 , GRCh37.p13 chr18: 12,000,673-12,871,098 RNU6-170P, ANKRD62, 24 more genes
    nsv6637316copy number variation1nstd102humanUncertain significance GRCh37 chr18: 11,290,617-15,106,305 , GRCh38.p12 chr18: 11,290,618-15,106,306 SNX19P3, LDLRAD4, 96 more genes
    nsv6637180copy number variation1nstd102humanUncertain significance GRCh37 chr18: 12,218,695-12,570,235 , GRCh38.p12 chr18: 12,218,696-12,570,236 HMGB3P28, C18orf61, 10 more genes
    nsv6635530copy number variation1nstd227human GRCh37 chr18: 11,930,945-12,236,187 , GRCh38.p12 chr18: 11,930,946-12,236,188 IMPA2, ANKRD62, 10 more genes
    nsv6533223copy number variation1nstd223human GRCh38 chr18: 12,171,601-12,442,300 , GRCh37.p13 chr18: 12,171,600-12,442,299 ANKRD62, TUBB6, 11 more genes
    nsv6529818copy number variation1nstd223human GRCh38 chr18: 12,201,501-12,205,000 , GRCh37.p13 chr18: 12,201,500-12,204,999 C18orf61
    nsv6528998copy number variation1nstd223human GRCh38 chr18: 12,219,201-12,228,700 , GRCh37.p13 chr18: 12,219,200-12,228,699 C18orf61
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