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Items: 1 to 20 of 313

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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
    nsv5875172copy number variation1nstd209human GRCh38 chr18: 63,641,642-63,644,242 , GRCh37.p13 chr18: 61,308,876-61,311,476 SERPINB4
    nsv5532857copy number variation1nstd206human GRCh38 chr18: 63,644,528-63,662,100 , GRCh37.p13 chr18: 61,311,762-61,329,334 SERPINB3, SERPINB4
    nsv5528996copy number variation1nstd206human GRCh38 chr18: 63,643,451-63,645,898 , GRCh37.p13 chr18: 61,310,685-61,313,132 SERPINB4
    nsv5528457copy number variation1nstd206human GRCh38 chr18: 63,642,528-63,660,528 , GRCh37.p13 chr18: 61,309,762-61,327,762 SERPINB3, SERPINB4
    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
    nsv5324449copy number variation1nstd204human GRCh38.p13 chr18: 63,643,537-63,645,907 , GRCh37.p13 chr18: 61,310,771-61,313,141 SERPINB4
    nsv5281152copy number variation1nstd204human GRCh38.p13 chr18: 63,636,567-63,652,347 , GRCh37.p13 chr18: 61,303,801-61,319,581 SERPINB4
    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
    nsv4859907copy number variation1nstd200human GRCh37 chr18: 61,310,814-61,313,159 , GRCh38.p12 chr18: 63,643,580-63,645,925 SERPINB4
    nsv4859906copy number variation1nstd200human GRCh37 chr18: 61,304,997-61,322,917 , GRCh38.p12 chr18: 63,637,763-63,655,683 SERPINB3, SERPINB4
    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
    nsv4634256copy number variation1nstd183human GRCh37 chr18: 61,297,275-61,303,558 , GRCh38.p12 chr18: 63,630,041-63,636,324 SERPINB4
    nsv4626823copy number variation1nstd183human GRCh37 chr18: 61,311,022-61,311,537 , GRCh38.p12 chr18: 63,643,788-63,644,303 SERPINB4
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