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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098917copy number variation1nstd102humanPathogenic GRCh37 chr18: 1-15,400,035 , GRCh38.p12 chr18: 10,001-15,400,036 RNU7-25P, RPL6P27, 275 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
    nsv7011056copy number variation1nstd229human GRCh38 chr18: 14,071,852-14,980,918 , GRCh37.p13 chr18: 14,071,851-14,980,917 OR4K7P, POTEC, 36 more genes
    nsv7010333copy number variation1nstd229human GRCh38 chr18: 14,768,987-14,784,468 , GRCh37.p13 chr18: 14,768,986-14,784,467 ANKRD30B, LOC105372008
    nsv7007961copy number variation1nstd229human GRCh38 chr18: 14,746,692-14,758,961 , GRCh37.p13 chr18: 14,746,691-14,758,960 RNU6-1210P, LOC105372007, 2 more genes
    nsv7007772copy number variation1nstd229human GRCh38 chr18: 13,577,365-14,771,703 , GRCh37.p13 chr18: 13,577,364-14,771,702 GRAMD4P7, RNU6-316P, 39 more genes
    nsv7007621copy number variation1nstd229human GRCh38 chr18: 14,755,620-14,773,383 , GRCh37.p13 chr18: 14,755,619-14,773,382 ANKRD30B, LOC105372008, 1 more genes
    nsv7005866copy number variation1nstd229human GRCh38 chr18: 14,741,547-14,763,336 , GRCh37.p13 chr18: 14,741,546-14,763,335 LOC105372008, ANKRD30B, 2 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
    nsv6624542copy number variation1nstd224human GRCh37 chr18: 14,660,464-14,791,236 , GRCh38.p12 chr18: 14,660,465-14,791,237 ANKRD30B, VN1R74P, 6 more genes
    nsv6624331copy number variation1nstd224human GRCh37 chr18: 14,715,283-15,286,251 , GRCh38.p12 chr18: 14,715,284-15,286,252 LOC284269, LINC01443, 16 more genes
    nsv6624135copy number variation4nstd224human GRCh37 chr18: 14,727,931-15,102,421 , GRCh38.p12 chr18: 14,727,932-15,102,422 ANKRD30B, MIR3156-2, 11 more genes
    nsv6594605inversion1nstd223human GRCh38 chr18: 14,764,459-14,765,293 , GRCh37.p13 chr18: 14,764,458-14,765,292 LOC105372008, ANKRD30B
    nsv6520814copy number variation1nstd223human GRCh38 chr18: 14,764,801-14,770,500 , GRCh37.p13 chr18: 14,764,800-14,770,499 LOC105372008, ANKRD30B
    nsv6520188copy number variation1nstd223human GRCh38 chr18: 14,769,601-14,772,500 , GRCh37.p13 chr18: 14,769,600-14,772,499 ANKRD30B, LOC105372008
    nsv6315530copy number variation1nstd102humanPathogenic GRCh37 chr18: 1-78,077,248 , GRCh38.p12 chr18: 10,001-80,259,271 LOC105372145, LOC105372016, 947 more genes
    nsv6315187copy number variation1nstd102humanPathogenic GRCh37 chr18: 47,390-14,854,037 , GRCh38.p12 chr18: 47,390-14,854,038 MIR4526, LINC01882, 261 more genes
    nsv6314722copy number variation1nstd102humanPathogenic GRCh37 chr18: 1,262,334-53,254,751 , GRCh38.p12 chr18: 1,262,333-55,587,520 LOC107985176, ZNF521, 632 more genes
    nsv6314195copy number variation1nstd102humanUncertain significance GRCh37 chr18: 14,715,282-18,988,457 , GRCh38.p12 chr18: 14,715,283-21,408,496 LOC105372008, LOC284269, 26 more genes
    nsv6291808copy number variation1nstd102humanLikely benign GRCh37 chr18: 14,710,374-15,181,666 , GRCh38.p12 chr18: 14,710,375-15,181,667 LINC01444, LOC105372010, 12 more genes
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