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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6116598mobile element insertion1nstd186human GRCh37 chr18: 53,146,061-53,146,061 , GRCh38.p12 chr18: 55,478,830-55,478,830 TCF4, MIR4529, 1 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
    nsv5968113insertion1nstd209human GRCh37.p13 chr18: 53,146,061-53,146,061 , GRCh38 chr18: 55,478,830-55,478,830 TCF4, MIR4529, 1 more genes
    nsv5947286copy number variation1nstd209human GRCh38 chr18: 55,440,002-55,440,806 , GRCh37.p13 chr18: 53,107,233-53,108,037 TCF4
    nsv5946520copy number variation1nstd209human GRCh38 chr18: 55,560,525-55,560,579 , GRCh37.p13 chr18: 53,227,756-53,227,810 TCF4
    nsv5943974copy number variation1nstd209human GRCh38 chr18: 55,330,003-55,332,173 , GRCh37.p13 chr18: 52,997,234-52,999,404 TCF4
    nsv5943337copy number variation1nstd209human GRCh38 chr18: 55,245,760-55,245,893 , GRCh37.p13 chr18: 52,912,991-52,913,124 TCF4
    nsv5939870copy number variation1nstd209human GRCh38 chr18: 55,606,160-55,606,413 , GRCh37.p13 chr18: 53,273,391-53,273,644 LOC105372126, TCF4
    nsv5930914copy number variation1nstd209human GRCh38 chr18: 55,325,049-55,325,103 , GRCh37.p13 chr18: 52,992,280-52,992,334 TCF4
    nsv5928993copy number variation1nstd209human GRCh38 chr18: 55,325,246-55,325,413 , GRCh37.p13 chr18: 52,992,477-52,992,644 TCF4
    nsv5927746copy number variation1nstd209human GRCh38 chr18: 55,444,216-55,450,370 , GRCh37.p13 chr18: 53,111,447-53,117,601 TCF4
    nsv5884786copy number variation1nstd209human GRCh38 chr18: 55,443,887-55,450,311 , GRCh37.p13 chr18: 53,111,118-53,117,542 TCF4
    nsv5882226copy number variation1nstd209human GRCh38 chr18: 55,590,089-55,592,090 , GRCh37.p13 chr18: 53,257,320-53,259,321 TCF4, LOC105372126
    nsv5870746copy number variation1nstd209human GRCh38 chr18: 55,587,454-55,588,532 , GRCh37.p13 chr18: 53,254,685-53,255,763 TCF4, LOC105372126
    nsv5718390mobile element insertion1nstd211human GRCh38 chr18: 55,542,834-55,542,834 , GRCh37.p13 chr18: 53,210,065-53,210,065 TCF4
    nsv5716988mobile element insertion1nstd211human GRCh38 chr18: 55,535,212-55,535,212 , GRCh37.p13 chr18: 53,202,443-53,202,443 TCF4
    nsv5713469mobile element insertion2nstd211human GRCh38 chr18: 55,478,844-55,478,844 , GRCh37.p13 chr18: 53,146,075-53,146,075 TCF4, MIR4529, 1 more genes
    nsv5709680mobile element insertion1nstd211human GRCh38 chr18: 55,327,170-55,327,170 , GRCh37.p13 chr18: 52,994,401-52,994,401 TCF4
    nsv5708345mobile element insertion1nstd211human GRCh38 chr18: 55,333,525-55,333,525 , GRCh37.p13 chr18: 53,000,756-53,000,756 TCF4
    nsv5707927mobile element insertion2nstd211human GRCh38 chr18: 55,324,550-55,324,550 , GRCh37.p13 chr18: 52,991,781-52,991,781 TCF4
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