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Items: 1 to 20 of 274

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6115405mobile element insertion1nstd186human GRCh37 chr18: 56,819,464-56,819,464 , GRCh38.p12 chr18: 59,152,232-59,152,232 SEC11C
    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
    nsv5973163insertion1nstd209human GRCh38 chr18: 59,152,232-59,152,232 , GRCh37.p13 chr18: 56,819,464-56,819,464 SEC11C
    nsv5713841mobile element insertion2nstd211human GRCh38 chr18: 59,152,245-59,152,245 , GRCh37.p13 chr18: 56,819,477-56,819,477 SEC11C
    nsv5653812insertion1nstd207human GRCh38 chr18: 59,152,232-59,152,232 , GRCh37.p13 chr18: 56,819,464-56,819,464 SEC11C
    nsv5418720mobile element insertion1nstd206human GRCh38 chr18: 59,152,232-59,152,232 , GRCh37.p13 chr18: 56,819,464-56,819,464 SEC11C
    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
    nsv5381190copy number variation1nstd102humanUncertain significance GRCh37 chr18: 55,225,777-56,940,458 , GRCh38.p12 chr18: 57,558,545-59,273,226 TRG-TCC6-1, RAX, 32 more genes
    nsv5150346mobile element insertion1nstd203human GRCh38 chr18: 59,152,232-59,152,245 , GRCh37.p13 chr18: 56,819,464-56,819,477 SEC11C
    nsv5149032mobile element insertion1nstd203human GRCh38 chr18: 59,152,229-59,152,232 , GRCh37.p13 chr18: 56,819,461-56,819,464 SEC11C
    nsv5147134mobile element insertion1nstd203human GRCh38 chr18: 59,152,239-59,152,245 , GRCh37.p13 chr18: 56,819,471-56,819,477 SEC11C
    nsv5143413mobile element insertion1nstd203human GRCh38 chr18: 59,152,233-59,152,245 , GRCh37.p13 chr18: 56,819,465-56,819,477 SEC11C
    nsv5141987mobile element insertion1nstd203human GRCh38 chr18: 59,156,164-59,156,181 , GRCh37.p13 chr18: 56,823,396-56,823,413 SEC11C
    nsv5018314copy number variation1nstd200human GRCh38 chr18: 59,148,219-59,152,545 , GRCh37.p13 chr18: 56,815,451-56,819,777 SEC11C
    nsv4859786copy number variation1nstd200human GRCh37 chr18: 56,815,451-56,819,777 , GRCh38.p12 chr18: 59,148,219-59,152,545 SEC11C
    nsv4754141insertion1nstd199human GRCh37 chr18: 56,819,471-56,819,471 , GRCh38.p12 chr18: 59,152,239-59,152,239 SEC11C
    nsv4723242insertion1nstd186human GRCh37 chr18: 56,819,464-56,819,464 , GRCh38.p12 chr18: 59,152,232-59,152,232 SEC11C
    nsv4692493mobile element insertion1nstd186human GRCh37 chr18: 56,819,477-56,819,477 , GRCh38.p12 chr18: 59,152,245-59,152,245 SEC11C
    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
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