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Items: 1 to 20 of 210

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6131601insertion1nstd186human GRCh37 chr16: 77,230,203-77,230,243 , GRCh38.p12 chr16: 77,196,306-77,196,346 MON1B
    nsv5974592insertion1nstd209human GRCh38 chr16: 77,196,295-77,196,295 , GRCh37.p13 chr16: 77,230,192-77,230,192 MON1B
    nsv5946031copy number variation1nstd209human GRCh38 chr16: 77,164,870-77,191,938 , GRCh37.p13 chr16: 77,198,767-77,225,835 MON1B
    nsv5713380mobile element insertion2nstd211human GRCh38 chr16: 77,196,306-77,196,306 , GRCh37.p13 chr16: 77,230,203-77,230,203 MON1B
    nsv5654457insertion1nstd207human GRCh38 chr16: 77,196,295-77,196,295 , GRCh37.p13 chr16: 77,230,192-77,230,192 MON1B
    nsv5650857insertion1nstd207human GRCh38 chr16: 77,200,291-77,200,291 , GRCh37.p13 chr16: 77,234,188-77,234,188 SYCE1L, MON1B
    nsv5537396insertion1nstd206human GRCh38 chr16: 77,196,306-77,196,346 , GRCh37.p13 chr16: 77,230,203-77,230,243 MON1B
    nsv5380785copy number variation1nstd102humanUncertain significance GRCh37 chr16: 77,225,119-77,401,620 , GRCh38.p12 chr16: 77,191,222-77,367,723 ADAMTS18, SYCE1L, 2 more genes
    nsv5159824mobile element insertion1nstd203human GRCh38 chr16: 77,196,294-77,196,306 , GRCh37.p13 chr16: 77,230,191-77,230,203 MON1B
    nsv5158974mobile element insertion1nstd203human GRCh38 chr16: 77,196,306-77,196,306 , GRCh37.p13 chr16: 77,230,203-77,230,203 MON1B
    nsv5158155mobile element insertion1nstd203human GRCh38 chr16: 77,196,297-77,196,306 , GRCh37.p13 chr16: 77,230,194-77,230,203 MON1B
    nsv5156266mobile element insertion1nstd203human GRCh38 chr16: 77,196,301-77,196,306 , GRCh37.p13 chr16: 77,230,198-77,230,203 MON1B
    nsv5154213mobile element insertion1nstd203human GRCh38 chr16: 77,196,296-77,196,306 , GRCh37.p13 chr16: 77,230,193-77,230,203 MON1B
    nsv5153907mobile element insertion1nstd203human GRCh38 chr16: 77,196,299-77,196,306 , GRCh37.p13 chr16: 77,230,196-77,230,203 MON1B
    nsv5142866mobile element insertion1nstd203human GRCh38 chr16: 77,196,298-77,196,306 , GRCh37.p13 chr16: 77,230,195-77,230,203 MON1B
    nsv5142339mobile element insertion1nstd203human GRCh38 chr16: 77,196,295-77,196,306 , GRCh37.p13 chr16: 77,230,192-77,230,203 MON1B
    nsv5034683inversion1nstd200human GRCh38 chr16: 60,098,351-77,500,042 , GRCh37.p13 chr16: 60,132,255-77,533,939 , TRG-GCC2-5, 313 more genes
    nsv5013411copy number variation1nstd200human GRCh38 chr16: 77,164,870-77,191,941 , GRCh37.p13 chr16: 77,198,767-77,225,838 MON1B
    nsv5013410copy number variation1nstd200human GRCh38 chr16: 77,157,335-77,192,799 , GRCh37.p13 chr16: 77,191,232-77,226,696 MON1B
    nsv5009408copy number variation1nstd200human GRCh38 chr16: 77,200,057-77,209,443 , GRCh37.p13 chr16: 77,233,954-77,243,340 SYCE1L, MON1B
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