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Items: 1 to 20 of 148

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5905992copy number variation1nstd209human GRCh38 chr5: 157,631,720-157,631,997 , GRCh37.p13 chr5: 157,058,728-157,059,005 SOX30
    nsv5893909copy number variation1nstd209human GRCh38 chr5: 157,636,001-157,636,139 , GRCh37.p13 chr5: 157,063,009-157,063,147 SOX30
    nsv5682085mobile element insertion1nstd211human GRCh38 chr5: 157,648,604-157,648,604 , GRCh37.p13 chr5: 157,075,612-157,075,612 SOX30
    nsv5680248mobile element insertion1nstd211human GRCh38 chr5: 157,656,346-157,656,346 , GRCh37.p13 chr5: 157,083,354-157,083,354 SOX30, LOC105377675
    nsv5636169insertion1nstd207human GRCh38 chr5: 157,631,053-157,631,053 , GRCh37.p13 chr5: 157,058,061-157,058,061 SOX30
    nsv5473120copy number variation1nstd206human GRCh38 chr5: 157,653,448-157,692,688 , GRCh37.p13 chr5: 157,080,456-157,119,696 C5orf52, LOC105377675, 2 more genes
    nsv5400535mobile element insertion1nstd206human GRCh38 chr5: 157,656,346-157,656,397 , GRCh37.p13 chr5: 157,083,354-157,083,405 LOC105377675, SOX30
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv4949120copy number variation1nstd200human GRCh38 chr5: 157,654,854-157,695,244 , GRCh37.p13 chr5: 157,081,862-157,122,252 LOC105377676, SOX30P1, 3 more genes
    nsv4939435copy number variation1nstd200human GRCh38 chr5: 157,653,422-157,692,579 , GRCh37.p13 chr5: 157,080,430-157,119,587 C5orf52, LOC105377675, 2 more genes
    nsv4939434copy number variation1nstd200human GRCh38 chr5: 157,640,607-157,649,922 , GRCh37.p13 chr5: 157,067,615-157,076,930 SOX30, LOC105377675
    nsv4939433copy number variation1nstd200human GRCh38 chr5: 157,624,886-157,626,329 , GRCh37.p13 chr5: 157,051,894-157,053,337 SOX30
    nsv4939432copy number variation1nstd200human GRCh38 chr5: 157,624,190-157,624,306 , GRCh37.p13 chr5: 157,051,198-157,051,314 SOX30
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4815148copy number variation1nstd200human GRCh37 chr5: 157,080,516-157,119,590 , GRCh38.p12 chr5: 157,653,508-157,692,582 LOC105377675, C5orf52, 2 more genes
    nsv4815147copy number variation1nstd200human GRCh37 chr5: 157,067,615-157,076,930 , GRCh38.p12 chr5: 157,640,607-157,649,922 SOX30, LOC105377675
    nsv4815146copy number variation1nstd200human GRCh37 chr5: 157,063,011-157,063,148 , GRCh38.p12 chr5: 157,636,003-157,636,140 SOX30
    nsv4815145copy number variation1nstd200human GRCh37 chr5: 157,051,894-157,053,337 , GRCh38.p12 chr5: 157,624,886-157,626,329 SOX30
    nsv4674945copy number variation1nstd102humanPathogenic GRCh37 chr5: 156,347,980-169,959,880 , GRCh38.p12 chr5: 156,920,969-170,532,876 LINC02227, LINC01932, 146 more genes
    nsv4494944mobile element insertion1nstd166human GRCh37.p13 chr5: 157,092,606-157,092,606 , GRCh38.p12 chr5: 157,665,598-157,665,598 SOX30
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