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Items: 1 to 20 of 242

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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
    nsv7076310inversion1nstd229human GRCh38 chr18: 7,168,687-9,983,107 , GRCh37.p13 chr18: 7,168,686-9,983,104 MTCL1, LOC112577592, 40 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
    nsv7016744copy number variation1nstd229human GRCh38 chr18: 9,884,203-9,884,549 , GRCh37.p13 chr18: 9,884,200-9,884,546 TXNDC2
    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
    nsv7013324copy number variation1nstd229human GRCh38 chr18: 9,888,390-9,896,849 , GRCh37.p13 chr18: 9,888,387-9,896,846 TXNDC2, LOC105371982
    nsv7003223copy number variation1nstd229human GRCh38 chr18: 9,804,909-10,534,004 , GRCh37.p13 chr18: 9,804,906-10,534,001 RNA5SP450, VAPA, 15 more genes
    nsv6637285copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,227-11,283,184 , GRCh38.p12 chr18: 136,227-11,283,185 EMILIN2, KRT18P8, 165 more genes
    nsv6521189copy number variation1nstd223human GRCh38 chr18: 9,881,310-9,891,815 , GRCh37.p13 chr18: 9,881,307-9,891,812 TXNDC2, PIGPP4
    nsv6315541copy number variation1nstd102humanPathogenic GRCh37 chr18: 9,569,601-12,218,695 , GRCh38.p12 chr18: 9,569,603-12,218,696 LOC105371989, LOC100533852, 55 more genes
    nsv6315536copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,226-10,172,941 , GRCh38.p12 chr18: 136,226-10,172,944 DLGAP1-AS5, TWSG1, 150 more genes
    nsv6315530copy number variation1nstd102humanPathogenic GRCh37 chr18: 1-78,077,248 , GRCh38.p12 chr18: 10,001-80,259,271 LOC105372145, LOC105372016, 947 more genes
    nsv6315508copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,226-14,632,436 , GRCh38.p12 chr18: 136,226-14,632,437 IGLJCOR18, MYOM1, 247 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
    nsv6314061copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,226-14,384,326 , GRCh38.p12 chr18: 136,226-14,384,327 LOC105371982, BOD1P2, 236 more genes
    nsv6313936copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,226-13,655,146 , GRCh38.p12 chr18: 136,226-13,655,147 LOC107985176, TYMSOS, 216 more genes
    nsv6291786copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,226-25,252,276 , GRCh38.p12 chr18: 136,226-27,672,312 LOC107985122, LOC100130487, 375 more genes
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