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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
    nsv7095430copy number variation1nstd102humanUncertain significance GRCh37 chr18: 12,329,564-12,377,081 , GRCh38.p12 chr18: 12,329,565-12,377,082 TUBB6, LOC107985154, 1 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
    nsv7074186inversion1nstd229human GRCh38 chr18: 7,953,048-15,343,982 , GRCh37.p13 chr18: 7,953,046-15,343,981 PSMG2, EIF4A2P1, 155 more genes
    nsv7016890copy number variation1nstd229human GRCh38 chr18: 12,327,098-12,331,447 , GRCh37.p13 chr18: 12,327,097-12,331,446 AFG3L2, TUBB6
    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
    nsv7006647copy number variation1nstd229human GRCh38 chr18: 12,261,209-12,427,634 , GRCh37.p13 chr18: 12,261,208-12,427,633 CIDEA, PRELID3A, 5 more genes
    nsv7005638copy number variation1nstd229human GRCh38 chr18: 12,318,987-12,322,367 , GRCh37.p13 chr18: 12,318,986-12,322,366 TUBB6
    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
    nsv7002143copy number variation1nstd229human GRCh38 chr18: 12,314,615-12,317,675 , GRCh37.p13 chr18: 12,314,614-12,317,674 TUBB6
    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
    nsv6637785copy number variation1nstd102humanUncertain significance GRCh37 chr18: 12,238,850-12,454,719 , GRCh38.p12 chr18: 12,238,851-12,454,720 PRELID3A, AFG3L2, 9 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
    nsv6637314copy number variation1nstd102humanUncertain significance GRCh37 chr18: 12,249,702-12,570,235 , GRCh38.p12 chr18: 12,249,703-12,570,236 LOC107985154, LOC105371996, 9 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
    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
    nsv6524552copy number variation1nstd223human GRCh38 chr18: 12,045,864-12,921,903 , GRCh37.p13 chr18: 12,045,863-12,921,902 RNU6-170P, ANKRD62, 25 more genes
    nsv6315530copy number variation1nstd102humanPathogenic GRCh37 chr18: 1-78,077,248 , GRCh38.p12 chr18: 10,001-80,259,271 LOC105372145, LOC105372016, 947 more genes
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