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Items: 1 to 20 of 306

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5952399insertion1nstd209human GRCh38 chr6: 87,407,647-87,407,647 , GRCh37.p13 chr6: 88,117,365-88,117,365 CFAP206
    nsv5902376copy number variation1nstd209human GRCh38 chr6: 87,408,455-87,408,587 , GRCh37.p13 chr6: 88,118,173-88,118,305 CFAP206
    nsv5894364copy number variation1nstd209human GRCh38 chr6: 87,429,239-87,433,586 , GRCh37.p13 chr6: 88,138,957-88,143,304 CFAP206
    nsv5846004copy number variation1nstd209human GRCh38 chr6: 87,429,175-87,434,474 , GRCh37.p13 chr6: 88,138,893-88,144,192 CFAP206
    nsv5721483mobile element insertion2nstd211human GRCh38 chr6: 87,407,663-87,407,663 , GRCh37.p13 chr6: 88,117,381-88,117,381 CFAP206
    nsv5692020mobile element insertion1nstd211human GRCh38 chr6: 87,415,978-87,415,978 , GRCh37.p13 chr6: 88,125,696-88,125,696 CFAP206
    nsv5629354insertion1nstd207human GRCh38 chr6: 87,407,647-87,407,647 , GRCh37.p13 chr6: 88,117,365-88,117,365 CFAP206
    nsv5626618insertion1nstd207human GRCh38 chr6: 87,408,455-87,408,455 , GRCh37.p13 chr6: 88,118,173-88,118,173 CFAP206
    nsv5579372copy number variation1nstd207human GRCh38 chr6: 87,408,455-87,408,587 , GRCh37.p13 chr6: 88,118,173-88,118,305 CFAP206
    nsv5560777mobile element insertion1nstd206human GRCh38 chr6: 87,407,663-87,407,714 , GRCh37.p13 chr6: 88,117,381-88,117,432 CFAP206
    nsv5457310copy number variation1nstd206human GRCh38 chr6: 87,429,244-87,433,587 , GRCh37.p13 chr6: 88,138,962-88,143,305 CFAP206
    nsv5457087copy number variation1nstd206human GRCh38 chr6: 87,408,477-87,408,588 , GRCh37.p13 chr6: 88,118,195-88,118,306 CFAP206
    nsv5387462copy number variation2nstd186human GRCh37 chr6: 88,118,195-88,118,306 , GRCh38.p12 chr6: 87,408,477-87,408,588 CFAP206
    nsv5369413translocation1nstd200human GRCh38 chr6: 87,429,244-87,429,244 , GRCh38 chr6: 87,433,587-87,433,587 , GRCh37.p13 chr6: 88,138,962-88,138,962 , GRCh37.p13 chr6: 88,143,305-88,143,305 CFAP206
    nsv5331191translocation1nstd200human GRCh37 chr6: 88,143,305-88,143,305 , GRCh37 chr6: 88,138,962-88,138,962 , GRCh38.p12 chr6: 87,433,587-87,433,587 , GRCh38.p12 chr6: 87,429,244-87,429,244 CFAP206
    nsv5312638copy number variation1nstd204human GRCh38.p13 chr6: 87,408,477-87,408,588 , GRCh37.p13 chr6: 88,118,195-88,118,306 CFAP206
    nsv5197923mobile element insertion1nstd203human GRCh38 chr6: 87,407,647-87,407,663 , GRCh37.p13 chr6: 88,117,365-88,117,381 CFAP206
    nsv5195781mobile element insertion1nstd203human GRCh38 chr6: 87,407,648-87,407,663 , GRCh37.p13 chr6: 88,117,366-88,117,381 CFAP206
    nsv5195502mobile element insertion1nstd203human GRCh38 chr6: 87,407,651-87,407,663 , GRCh37.p13 chr6: 88,117,369-88,117,381 CFAP206
    nsv5194149mobile element insertion1nstd203human GRCh38 chr6: 87,407,649-87,407,663 , GRCh37.p13 chr6: 88,117,367-88,117,381 CFAP206
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