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Items: 1 to 20 of 370

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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
    nsv5525679copy number variation1nstd206human GRCh38 chr18: 62,372,489-62,372,558 , GRCh37.p13 chr18: 60,039,722-60,039,791 TNFRSF11A
    nsv5524050copy number variation1nstd206human GRCh38 chr18: 62,324,486-62,324,541 , GRCh37.p13 chr18: 59,991,719-59,991,774 TNFRSF11A
    nsv5518838copy number variation1nstd206human GRCh38 chr18: 62,332,318-62,332,688 , GRCh37.p13 chr18: 59,999,551-59,999,921 TNFRSF11A
    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
    nsv5381191copy number variation1nstd102humanUncertain significance GRCh37 chr18: 59,805,466-60,131,307 , GRCh38.p12 chr18: 62,138,233-62,464,074 PIGN, RELCH, 3 more genes
    nsv4881550inversion1nstd200human GRCh37 chr18: 57,639,759-62,087,901 , GRCh38.p12 chr18: 59,972,527-64,420,666 , RPL17P44, 59 more genes
    nsv4859872copy number variation1nstd200human GRCh37 chr18: 59,999,551-59,999,921 , GRCh38.p12 chr18: 62,332,318-62,332,688 TNFRSF11A
    nsv4681624copy number variation1nstd102humanPathogenic GRCh37 chr18: 59,713,069-60,131,307 , GRCh38.p12 chr18: 62,045,836-62,464,074 ACTBP9, TNFRSF11A, 3 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
    nsv4632433copy number variation1nstd183human GRCh37 chr18: 59,937,087-60,008,461 , GRCh38.p12 chr18: 62,269,854-62,341,228 TNFRSF11A, RELCH
    nsv4626518copy number variation1nstd183human GRCh37 chr18: 59,941,016-60,007,022 , GRCh38.p12 chr18: 62,273,783-62,339,789 TNFRSF11A, RELCH
    nsv4512032mobile element insertion1nstd166human GRCh37.p13 chr18: 60,041,883-60,041,883 , GRCh38.p12 chr18: 62,374,650-62,374,650 TNFRSF11A
    nsv4503707mobile element insertion1nstd166human GRCh37.p13 chr18: 60,007,170-60,007,170 , GRCh38.p12 chr18: 62,339,937-62,339,937 TNFRSF11A
    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
    nsv4450642copy number variation1nstd102humanUncertain significance GRCh37 chr18: 59,713,069-60,131,307 , GRCh38 chr18: 62,045,836-62,464,074 RPL17P44, TNFRSF11A, 3 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
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