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Items: 1 to 20 of 337

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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
    nsv5707104mobile element insertion2nstd211human GRCh38 chr18: 63,482,719-63,482,719 , GRCh37.p13 chr18: 61,149,952-61,149,952 SERPINB5
    nsv5514135copy number variation1nstd206human GRCh38 chr18: 62,909,528-80,261,528 , GRCh37.p13 chr18: 60,576,761-78,017,154 , SMIM21, 190 more genes
    nsv5432679mobile element insertion1nstd206human GRCh38 chr18: 63,482,719-63,482,770 , GRCh37.p13 chr18: 61,149,952-61,150,003 SERPINB5
    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
    nsv5168408mobile element insertion1nstd203human GRCh38 chr18: 63,482,700-63,482,719 , GRCh37.p13 chr18: 61,149,933-61,149,952 SERPINB5
    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
    nsv4717332mobile element insertion1nstd186human GRCh37 chr18: 61,149,933-61,149,933 , GRCh38.p12 chr18: 63,482,700-63,482,700 SERPINB5
    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
    nsv4621848copy number variation1nstd183human GRCh37 chr18: 61,171,937-61,174,140 , GRCh38.p12 chr18: 63,504,704-63,506,907 SERPINB5
    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
    nsv4514230mobile element insertion1nstd166human GRCh37.p13 chr18: 61,149,933-61,149,933 , GRCh38.p12 chr18: 63,482,700-63,482,700 SERPINB5
    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
    nsv4420782copy number variation1nstd174human GRCh37 chr18: 61,171,915-61,174,745 , GRCh38.p12 chr18: 63,504,682-63,507,512 SERPINB5
    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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