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Items: 1 to 20 of 243

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112815copy number variation1nstd102humanPathogenic GRCh37 chr18: 54,285,235-77,960,815 , GRCh38.p12 chr18: 56,618,004-80,202,932 RPL31P9, TRG-TCC5-1, 271 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
    nsv5719433mobile element insertion1nstd211human GRCh38 chr18: 61,752,491-61,752,491 , GRCh37.p13 chr18: 59,419,724-59,419,724 LINC01544
    nsv5381802copy number variation1nstd102humanPathogenic GRCh37 chr18: 51,925,586-78,010,032 , GRCh38.p12 chr18: 54,399,216-80,252,149 LOC105372200, LOC105372174, 298 more genes
    nsv5321051copy number variation1nstd204human GRCh38.p13 chr18: 59,841,074-61,898,517 , GRCh37.p13 chr18: 57,508,306-59,565,750 LINC01544, LSM6P1, 28 more genes
    nsv5292002copy number variation1nstd204human GRCh38.p13 chr18: 61,735,590-61,775,543 , GRCh37.p13 chr18: 59,402,823-59,442,776 LINC01544
    nsv5285222copy number variation1nstd204human GRCh37.p13 chr18: 58,877,834-59,565,433 , GRCh38.p13 chr18: 61,210,601-61,898,200 CDH20, RNF152, 7 more genes
    nsv5018421copy number variation1nstd200human GRCh38 chr18: 61,747,625-61,748,661 , GRCh37.p13 chr18: 59,414,858-59,415,894 LINC01544
    nsv5018419copy number variation1nstd200human GRCh38 chr18: 61,728,802-61,800,866 , GRCh37.p13 chr18: 59,396,035-59,468,099 LINC01544
    nsv5018412copy number variation1nstd200human GRCh38 chr18: 61,572,231-61,914,284 , GRCh37.p13 chr18: 59,239,464-59,581,517 RNF152, LSM6P1, 4 more genes
    nsv4881550inversion1nstd200human GRCh37 chr18: 57,639,759-62,087,901 , GRCh38.p12 chr18: 59,972,527-64,420,666 , RPL17P44, 59 more genes
    nsv4859855copy number variation1nstd200human GRCh37 chr18: 59,414,858-59,415,894 , GRCh38.p12 chr18: 61,747,625-61,748,661 LINC01544
    nsv4859854copy number variation1nstd200human GRCh37 chr18: 59,396,035-59,468,099 , GRCh38.p12 chr18: 61,728,802-61,800,866 LINC01544
    nsv4854731copy number variation1nstd200human GRCh37 chr18: 57,508,482-59,565,529 , GRCh38.p12 chr18: 59,841,250-61,898,296 RN7SL342P, RPS3AP49, 28 more genes
    nsv4676378copy number variation1nstd102humanPathogenic GRCh37 chr18: 56,750,525-78,014,123 , GRCh38.p12 chr18: 59,083,293-80,256,240 HSBP1L1, TXNL4A, 231 more genes
    nsv4676158copy number variation1nstd102humanPathogenic GRCh37 chr18: 55,458,425-78,014,123 , GRCh38.p12 chr18: 57,791,193-80,256,240 LOC105372140, LOC105372143, 253 more genes
    nsv4676105copy number variation1nstd102humanPathogenic GRCh37 chr18: 49,460,596-78,014,123 , GRCh38.p12 chr18: 51,934,226-80,256,240 MIR548AV, GTSCR1, 310 more genes
    nsv4457866copy number variation1nstd102humanPathogenic GRCh37 chr18: 45,621,155-61,416,536 , GRCh38.p12 chr18: 48,094,784-63,749,302 LOC105372159, LOC105372156, 208 more genes
    nsv4346369copy number variation1nstd102humanPathogenic GRCh37 chr18: 58,024,137-77,996,821 , GRCh38.p12 chr18: 60,356,904-80,238,938 LOC105372221, LINC00683, 206 more genes
    nsv4336672sequence alteration1nstd166human GRCh37.p13 chr18: 21,176,191-70,772,863 , GRCh38.p12 chr18: 23,596,227-73,105,628 , CDH2, 557 more genes
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