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Items: 1 to 20 of 395

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095449copy number variation1nstd102humanPathogenic GRCh37 chr18: 60,015,381-60,017,190 , GRCh38.p12 chr18: 62,348,148-62,349,957 TNFRSF11A
    nsv7095448copy number variation1nstd102humanUncertain significance GRCh37 chr18: 59,805,456-60,052,267 , GRCh38.p12 chr18: 62,138,223-62,385,034 PIGN, TNFRSF11A, 1 more genes
    nsv7072414inversion1nstd229human GRCh38 chr18: 59,526,812-66,942,199 , GRCh37.p13 chr18: 57,194,044-64,609,436 RPIAP1, LOC105372167, 77 more genes
    nsv7071501inversion1nstd229human GRCh38 chr18: 62,269,541-62,333,423 , GRCh37.p13 chr18: 59,936,774-60,000,656 RELCH, TNFRSF11A
    nsv7069827inversion1nstd229human GRCh38 chr18: 60,254,377-67,312,517 , GRCh37.p13 chr18: 57,921,610-64,979,754 RNU6-142P, TNFRSF11A, 63 more genes
    nsv7066376inversion1nstd229human GRCh38 chr18: 61,808,565-71,004,929 , GRCh37.p13 chr18: 59,475,798-68,672,165 DSEL-AS1, LOC112268209, 84 more genes
    nsv7064880inversion1nstd229human GRCh38 chr18: 62,333,430-62,341,346 , GRCh37.p13 chr18: 60,000,663-60,008,579 TNFRSF11A
    nsv7014166copy number variation1nstd229human GRCh38 chr18: 62,375,652-62,375,847 , GRCh37.p13 chr18: 60,042,885-60,043,080 TNFRSF11A
    nsv7013777copy number variation1nstd229human GRCh38 chr18: 62,391,781-62,398,151 , GRCh37.p13 chr18: 60,059,014-60,065,384 TNFRSF11A
    nsv7010330copy number variation1nstd229human GRCh38 chr18: 62,320,748-62,331,732 , GRCh37.p13 chr18: 59,987,981-59,998,965 TNFRSF11A
    nsv6637467copy number variation1nstd102humanPathogenic GRCh37 chr18: 53,624,405-78,014,123 , GRCh38.p12 chr18: 55,957,174-80,256,240 RPL9P31, LOC100422317, 277 more genes
    nsv6624803copy number variation1nstd224human GRCh37 chr18: 59,941,236-60,000,477 , GRCh38.p12 chr18: 62,274,003-62,333,244 TNFRSF11A, RELCH
    nsv6519402copy number variation1nstd223human GRCh38 chr18: 62,324,601-62,326,000 , GRCh37.p13 chr18: 59,991,834-59,993,233 TNFRSF11A
    nsv6315530copy number variation1nstd102humanPathogenic GRCh37 chr18: 1-78,077,248 , GRCh38.p12 chr18: 10,001-80,259,271 LOC105372145, LOC105372016, 947 more genes
    nsv6315301copy number variation1nstd102humanPathogenic GRCh38 chr18: 61,490,305-80,247,612 , GRCh37.p13 chr18: 59,157,538-78,005,495 RN7SL705P, LOC105372166, 196 more genes
    nsv6314216copy number variation1nstd102humanPathogenic GRCh37 chr18: 52,675,201-78,014,123 , GRCh38.p12 chr18: 55,007,970-80,256,240 RNA5SP461, CYB5A, 290 more genes
    nsv6314188copy number variation1nstd102humanPathogenic GRCh37 chr18: 53,309,113-78,014,123 , GRCh38.p12 chr18: 55,641,882-80,256,240 ZNF236-DT, SERPINB2, 282 more genes
    nsv6314111copy number variation1nstd102humanPathogenic GRCh37 chr18: 58,305,972-78,014,123 , GRCh38.p12 chr18: 60,638,739-80,256,240 LOC101927897, CTDP1, 202 more genes
    nsv6310450copy number variation1nstd102humanUncertain significance GRCh37 chr18: 59,992,586-59,992,680 , GRCh38.p12 chr18: 62,325,353-62,325,447 TNFRSF11A
    nsv6310364copy number variation1nstd102humanUncertain significance GRCh37 chr18: 60,015,381-60,034,013 , GRCh38.p12 chr18: 62,348,148-62,366,780 TNFRSF11A
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