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Items: 1 to 20 of 522

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5963411insertion1nstd209human GRCh38 chr5: 139,057,314-139,057,314 , GRCh37.p13 chr5: 138,393,003-138,393,003 SIL1
    nsv5957756insertion1nstd209human GRCh38 chr5: 139,155,448-139,155,448 , GRCh37.p13 chr5: 138,491,137-138,491,137 SIL1
    nsv5951045insertion1nstd209human GRCh38 chr5: 139,037,106-139,037,106 , GRCh37.p13 chr5: 138,372,795-138,372,795 SIL1
    nsv5904985copy number variation1nstd209human GRCh38 chr5: 138,955,676-138,955,992 , GRCh37.p13 chr5: 138,291,365-138,291,681 SIL1
    nsv5900299copy number variation1nstd209human GRCh38 chr5: 138,984,604-138,984,664 , GRCh37.p13 chr5: 138,320,293-138,320,353 SIL1
    nsv5899457copy number variation1nstd209human GRCh38 chr5: 139,146,032-139,146,835 , GRCh37.p13 chr5: 138,481,721-138,482,524 SIL1
    nsv5895803copy number variation1nstd209human GRCh38 chr5: 139,046,653-139,046,710 , GRCh37.p13 chr5: 138,382,342-138,382,399 SIL1
    nsv5895009copy number variation1nstd209human GRCh38 chr5: 139,177,167-139,177,472 , GRCh37.p13 chr5: 138,512,856-138,513,161 SIL1
    nsv5890005copy number variation1nstd209human GRCh38 chr5: 138,955,730-138,971,631 , GRCh37.p13 chr5: 138,291,419-138,307,320 , SIL1
    nsv5841776copy number variation1nstd209human GRCh38 chr5: 138,963,736-138,965,035 , GRCh37.p13 chr5: 138,299,425-138,300,724 , SIL1
    nsv5841693copy number variation1nstd209human GRCh38 chr5: 138,955,579-138,971,610 , GRCh37.p13 chr5: 138,291,268-138,307,299 , SIL1
    nsv5715707mobile element insertion2nstd211human GRCh38 chr5: 139,037,120-139,037,120 , GRCh37.p13 chr5: 138,372,809-138,372,809 SIL1
    nsv5684955mobile element insertion1nstd211human GRCh38 chr5: 139,159,289-139,159,289 , GRCh37.p13 chr5: 138,494,978-138,494,978 SIL1
    nsv5627838insertion1nstd207human GRCh38 chr5: 139,037,106-139,037,106 , GRCh37.p13 chr5: 138,372,795-138,372,795 SIL1
    nsv5582646copy number variation1nstd207human GRCh38 chr5: 139,170,795-139,170,921 , GRCh37.p13 chr5: 138,506,484-138,506,610 SIL1
    nsv5570788copy number variation1nstd207human GRCh38 chr5: 138,951,052-138,951,115 , GRCh37.p13 chr5: 138,286,741-138,286,804 SIL1
    nsv5563509sequence alteration1nstd206human GRCh38 chr5: 138,934,774-138,945,833 , GRCh37.p13 chr5: 138,270,463-138,281,522 CTNNA1, SIL1
    nsv5471898copy number variation1nstd206human GRCh38 chr5: 139,062,838-139,113,688 , GRCh37.p13 chr5: 138,398,527-138,449,377 SIL1
    nsv5470974copy number variation1nstd206human GRCh38 chr5: 138,993,982-139,000,361 , GRCh37.p13 chr5: 138,329,671-138,336,050 SIL1
    nsv5468778copy number variation1nstd206human GRCh38 chr5: 138,964,846-138,964,923 , GRCh37.p13 chr5: 138,300,535-138,300,612 , SIL1
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