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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112778copy number variation1nstd102humanPathogenic GRCh37 chr20: 51,799,648-62,916,626 , GRCh38.p12 chr20: 53,183,109-64,285,273 LINC01742, MTCO2P1, 253 more genes
    nsv5962572copy number variation1nstd209human GRCh38 chr20: 63,731,457-63,731,560 , GRCh37.p13 chr20: 62,362,809-62,362,912 ZGPAT
    nsv5955909copy number variation1nstd209human GRCh38 chr20: 63,730,123-63,731,058 , GRCh37.p13 chr20: 62,361,475-62,362,410 ZGPAT
    nsv5952126copy number variation1nstd209human GRCh38 chr20: 63,731,302-63,731,567 , GRCh37.p13 chr20: 62,362,654-62,362,919 ZGPAT
    nsv5715817mobile element insertion2nstd211human GRCh38 chr20: 63,726,150-63,726,150 , GRCh37.p13 chr20: 62,357,502-62,357,502 ZGPAT
    nsv5600495copy number variation1nstd207human GRCh38 chr20: 63,723,394-63,723,477 , GRCh37.p13 chr20: 62,354,746-62,354,829 ZGPAT
    nsv5599625copy number variation1nstd207human GRCh38 chr20: 63,731,457-63,731,560 , GRCh37.p13 chr20: 62,362,809-62,362,912 ZGPAT
    nsv5562694sequence alteration1nstd206human GRCh38 chr20: 63,525,502-63,937,515 , GRCh37.p13 chr20: 62,156,855-62,568,868 , STMN3, 26 more genes
    nsv5559866sequence alteration1nstd206human GRCh38 chr20: 62,865,770-63,725,218 , GRCh37.p13 chr20: 61,497,122-62,356,570 , PTK6, 46 more genes
    nsv5543138insertion1nstd206human GRCh38 chr20: 63,726,150-63,726,182 , GRCh37.p13 chr20: 62,357,502-62,357,534 ZGPAT
    nsv5523849copy number variation1nstd206human GRCh38 chr20: 63,730,647-63,730,763 , GRCh37.p13 chr20: 62,361,999-62,362,115 ZGPAT
    nsv5522769copy number variation1nstd206human GRCh38 chr20: 63,729,971-63,733,398 , GRCh37.p13 chr20: 62,361,323-62,364,750 ZGPAT
    nsv5381223copy number variation2nstd102humanUncertain significance GRCh37 chr20: 60,831,241-62,664,346 , GRCh38.p12 chr20: 62,256,185-64,032,993 KCNQ2-AS1, HAR1B, 100 more genes
    nsv5321850copy number variation1nstd204human GRCh38.p13 chr20: 63,711,711-63,719,829 , GRCh37.p13 chr20: 62,343,063-62,351,181 ZGPAT
    nsv5298148copy number variation1nstd204human GRCh38.p13 chr20: 63,711,651-63,718,965 , GRCh37.p13 chr20: 62,343,003-62,350,317 ZGPAT
    nsv5295992copy number variation1nstd204human GRCh38.p13 chr20: 63,711,701-63,719,800 , GRCh37.p13 chr20: 62,343,053-62,351,152 ZGPAT
    nsv5293467copy number variation1nstd204human GRCh38.p13 chr20: 62,966,101-64,149,200 , GRCh37.p13 chr20: 61,597,453-62,780,553 , ZGPAT, 72 more genes
    nsv5293041copy number variation1nstd204human GRCh38.p13 chr20: 63,709,801-63,711,800 , GRCh37.p13 chr20: 62,341,153-62,343,152 ZGPAT
    nsv5292339copy number variation1nstd204human GRCh38.p13 chr20: 63,710,037-63,712,136 , GRCh37.p13 chr20: 62,341,389-62,343,488 ZGPAT
    nsv5172985mobile element insertion1nstd203human GRCh38 chr20: 63,717,320-63,717,357 , GRCh37.p13 chr20: 62,348,672-62,348,709 ZGPAT
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