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Items: 1 to 20 of 231

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7074210inversion1nstd229human GRCh38 chr18: 45,861,287-52,164,943 , GRCh37.p13 chr18: 43,441,252-49,691,313 LOC105372100, RNA5SP458, 103 more genes
    nsv7065765inversion1nstd229human GRCh38 chr18: 46,426,327-48,440,063 , GRCh37.p13 chr18: 44,006,290-45,966,434 ZBTB7C, MIR4527, 29 more genes
    nsv7062073inversion1nstd229human GRCh38 chr18: 42,140,183-50,368,023 , GRCh37.p13 chr18: 39,720,147-47,894,393 ACAA2, MIR4320, 105 more genes
    nsv7060607inversion1nstd229human GRCh38 chr18: 46,563,922-48,670,215 , GRCh37.p13 chr18: 44,143,885-46,196,586 SKOR2, ELOA3DP, 32 more genes
    nsv6998773copy number variation1nstd229human GRCh38 chr18: 44,716,377-50,773,277 , GRCh37.p13 chr18: 42,296,342-48,299,647 LOC105372101, MTCO2P2, 95 more genes
    nsv6998560copy number variation1nstd229human GRCh38 chr18: 46,921,465-47,196,235 , GRCh37.p13 chr18: 44,501,428-44,722,606 ELOA3CP, ELOA2, 8 more genes
    nsv6315530copy number variation1nstd102humanPathogenic GRCh37 chr18: 1-78,077,248 , GRCh38.p12 chr18: 10,001-80,259,271 LOC105372145, LOC105372016, 947 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
    nsv6291497copy number variation1nstd102humanUncertain significance GRCh37 chr18: 44,552,943-44,605,249 , GRCh38.p12 chr18: 47,026,572-47,078,878 ELOA2, KATNAL2, 2 more genes
    nsv6133445copy number variation1nstd213human GRCh37 chr18: 44,060,000-45,480,001 , GRCh38.p12 chr18: 46,480,037-47,953,630 SMAD2, PIAS2, 24 more genes
    nsv6133439copy number variation1nstd213human GRCh37 chr18: 28,680,000-49,600,001 , GRCh38.p12 chr18: 31,100,037-52,073,631 ATP5F1A, DSC1, 240 more genes
    nsv6133333copy number variation1nstd213human GRCh37 chr18: 27,400,000-52,060,001 , GRCh38.p12 chr18: 29,820,035-54,532,766 ATP5F1A, DCC, 259 more genes
    nsv6113333copy number variation1nstd186human GRCh37 chr18: 44,549,876-44,557,421 , GRCh38.p12 chr18: 47,023,505-47,031,050 ELOA2, KATNAL2, 2 more genes
    nsv6112802copy number variation1nstd102humanPathogenic GRCh37 chr18: 23,626,739-78,014,976 , GRCh38.p12 chr18: 26,046,775-80,257,093 RPL9P31, LINC02582, 595 more genes
    nsv6027991copy number variation1nstd212human GRCh38 chr18: 47,019,913-47,031,654 , GRCh37.p13 chr18: 44,549,876-44,558,025 ELOA2, KATNAL2, 2 more genes
    nsv5970228inversion1nstd209human GRCh38 chr18: 42,666,448-47,133,105 , GRCh37.p13 chr18: 40,246,413-44,659,476 , ATP5F1A, 50 more genes
    nsv5875322copy number variation1nstd209human GRCh38 chr18: 47,022,976-47,043,592 , GRCh37.p13 chr18: 44,549,876-44,569,963 ELOA3P, KATNAL2, 2 more genes
    nsv5433024copy number variation1nstd206human GRCh38 chr18: 47,019,956-47,031,050 , GRCh37.p13 chr18: 44,549,876-44,557,421 KATNAL2, ELOA3BP, 2 more genes
    nsv5381046copy number variation2nstd102humanUncertain significance GRCh37 chr18: 42,281,312-45,423,127 , GRCh38.p12 chr18: 44,701,347-47,896,756 HDHD2, RNU6-1131P, 45 more genes
    nsv5297342copy number variation1nstd204human GRCh38.p13 chr18: 47,029,001-47,030,400 , GRCh37.p13 chr18: 44,555,372-44,556,771 ELOA3P, KATNAL2
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