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Items: 1 to 20 of 294

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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
    nsv5514135copy number variation1nstd206human GRCh38 chr18: 62,909,528-80,261,528 , GRCh37.p13 chr18: 60,576,761-78,017,154 , SMIM21, 190 more genes
    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
    nsv5024293copy number variation1nstd200human GRCh38 chr18: 63,393,299-66,863,196 , GRCh37.p13 chr18: 61,060,532-64,530,433 PRPF19P1, VPS4B, 28 more genes
    nsv4881550inversion1nstd200human GRCh37 chr18: 57,639,759-62,087,901 , GRCh38.p12 chr18: 59,972,527-64,420,666 , RPL17P44, 59 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
    nsv4676217copy number variation1nstd102humanPathogenic GRCh37 chr18: 60,098,018-78,014,123 , GRCh38.p12 chr18: 62,430,785-80,256,240 HNRNPA1P11, ZNF236, 184 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
    nsv4545744insertion1nstd166human GRCh37.p13 chr18: 61,261,539-61,261,539 , GRCh38.p12 chr18: 63,594,305-63,594,305 SERPINB13
    nsv4532157copy number variation1nstd166human GRCh37.p13 chr18: 61,081,999-61,321,000 , GRCh38.p12 chr18: 63,414,766-63,653,766 SERPINB5, SERPINB13, 6 more genes
    nsv4505795mobile element insertion1nstd166human GRCh37.p13 chr18: 61,256,738-61,256,738 , GRCh38.p12 chr18: 63,589,504-63,589,504 SERPINB13
    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
    nsv4337437sequence alteration1nstd166human GRCh37.p13 chr18: 61,264,337-61,267,352 , GRCh38.p12 chr18: 63,597,103-63,600,118 SERPINB13
    nsv4336672sequence alteration1nstd166human GRCh37.p13 chr18: 21,176,191-70,772,863 , GRCh38.p12 chr18: 23,596,227-73,105,628 , CDH2, 557 more genes
    nsv3941916copy number variation1nstd167human GRCh37 chr18: 61,258,600-61,258,644 , GRCh38.p12 chr18: 63,591,366-63,591,410 SERPINB13
    nsv3924706copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,227-78,014,123 , GRCh38 chr18: 136,227-80,256,240 , NCBI36 chr18: 126,227-76,115,097 LOC100420948, NPM1P2, 941 more genes
    nsv3924638copy number variation1nstd102humanPathogenic GRCh38 chr18: 20,962,119-74,691,446 , NCBI36 chr18: 16,796,078-70,532,390 , GRCh37 chr18: 18,542,080-72,403,402 HMGN1P30, LOC107985134, 596 more genes
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