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Items: 1 to 20 of 601

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6116390mobile element insertion1nstd186human GRCh37 chr22: 50,273,380-50,273,406 , GRCh38.p12 chr22: 49,879,732-49,879,758 ZBED4, ALG12
    nsv6112794copy number variation1nstd102humanPathogenic GRCh37 chr22: 50,099,570-51,187,115 , GRCh38.p12 chr22: 49,705,922-50,748,687 SCO2, CIMAP1B, 50 more genes
    nsv5972028insertion1nstd209human GRCh38 chr22: 49,901,758-49,901,758 , GRCh37.p13 chr22: 50,295,406-50,295,406 ALG12
    nsv5970934insertion1nstd209human GRCh38 chr22: 49,917,986-49,917,986 , GRCh37.p13 chr22: 50,311,634-50,311,634 ALG12, CRELD2
    nsv5961747copy number variation1nstd209human GRCh38 chr22: 49,908,307-49,908,358 , GRCh37.p13 chr22: 50,301,955-50,302,006 ALG12
    nsv5959721copy number variation1nstd209human GRCh38 chr22: 49,860,838-49,865,071 , GRCh37.p13 chr22: 50,254,486-50,258,719 ZBED4, ALG12
    nsv5956807copy number variation1nstd209human GRCh38 chr22: 49,912,057-49,912,109 , GRCh37.p13 chr22: 50,305,705-50,305,757 ALG12
    nsv5952309copy number variation1nstd209human GRCh38 chr22: 49,901,503-49,901,558 , GRCh37.p13 chr22: 50,295,151-50,295,206 ALG12
    nsv5951553copy number variation1nstd209human GRCh38 chr22: 49,908,358-49,908,781 , GRCh37.p13 chr22: 50,302,006-50,302,429 ALG12
    nsv5948187copy number variation1nstd209human GRCh38 chr22: 49,901,554-49,901,756 , GRCh37.p13 chr22: 50,295,202-50,295,404 ALG12
    nsv5878243copy number variation1nstd209human GRCh38 chr22: 49,872,654-49,874,603 , GRCh37.p13 chr22: 50,266,302-50,268,251 ZBED4, ALG12
    nsv5871167copy number variation1nstd209human GRCh38 chr22: 49,860,902-49,865,153 , GRCh37.p13 chr22: 50,254,550-50,258,801 ZBED4, ALG12
    nsv5710442mobile element insertion1nstd211human GRCh38 chr22: 49,917,718-49,917,718 , GRCh37.p13 chr22: 50,311,366-50,311,366 ALG12, CRELD2
    nsv5695746mobile element insertion2nstd211human GRCh38 chr22: 49,879,732-49,879,732 , GRCh37.p13 chr22: 50,273,380-50,273,380 ALG12, ZBED4
    nsv5673438copy number variation1nstd102humanPathogenic GRCh37 chr22: 50,297,466-51,066,227 , GRCh38.p12 chr22: 49,903,818-50,627,799 MIR6821, CHKB, 39 more genes
    nsv5668609insertion1nstd207human GRCh38 chr22: 49,911,984-49,911,984 , GRCh37.p13 chr22: 50,305,632-50,305,632 ALG12
    nsv5667233insertion1nstd207human GRCh38 chr22: 49,879,746-49,879,746 , GRCh37.p13 chr22: 50,273,394-50,273,394 ZBED4, ALG12
    nsv5667167insertion1nstd207human GRCh38 chr22: 49,901,758-49,901,758 , GRCh37.p13 chr22: 50,295,406-50,295,406 ALG12
    nsv5666447insertion1nstd207human GRCh38 chr22: 49,917,986-49,917,986 , GRCh37.p13 chr22: 50,311,634-50,311,634 ALG12, CRELD2
    nsv5604128copy number variation1nstd207human GRCh38 chr22: 49,879,725-49,879,808 , GRCh37.p13 chr22: 50,273,373-50,273,456 ZBED4, ALG12
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