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Items: 1 to 20 of 910

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112754copy number variation1nstd102humanPathogenic GRCh37 chr4: 131,303,317-168,722,402 , GRCh38.p12 chr4: 130,382,162-167,801,251 MIR3139, CLGN, 407 more genes
    nsv5900754copy number variation1nstd209human GRCh38 chr4: 148,174,121-148,174,674 , GRCh37.p13 chr4: 149,095,272-149,095,825 NR3C2
    nsv5900509copy number variation1nstd209human GRCh38 chr4: 148,261,286-148,261,384 , GRCh37.p13 chr4: 149,182,438-149,182,536 NR3C2
    nsv5888387copy number variation1nstd209human GRCh38 chr4: 148,178,145-148,180,468 , GRCh37.p13 chr4: 149,099,296-149,101,619 NR3C2
    nsv5838056copy number variation1nstd209human GRCh38 chr4: 148,147,638-148,148,737 , GRCh37.p13 chr4: 149,068,789-149,069,888 NR3C2
    nsv5837742copy number variation1nstd209human GRCh38 chr4: 148,178,135-148,180,482 , GRCh37.p13 chr4: 149,099,286-149,101,633 NR3C2
    nsv5725847mobile element insertion1nstd211human GRCh38 chr4: 148,307,846-148,307,846 , GRCh37.p13 chr4: 149,228,998-149,228,998 NR3C2
    nsv5720415mobile element insertion1nstd211human GRCh38 chr4: 148,307,882-148,307,882 , GRCh37.p13 chr4: 149,229,034-149,229,034 NR3C2
    nsv5692651mobile element insertion1nstd211human GRCh38 chr4: 148,422,041-148,422,041 , GRCh37.p13 chr4: 149,343,193-149,343,193 NR3C2
    nsv5688533mobile element insertion2nstd211human GRCh38 chr4: 148,337,323-148,337,323 , GRCh37.p13 chr4: 149,258,475-149,258,475 NR3C2
    nsv5681432mobile element insertion1nstd211human GRCh38 chr4: 148,399,968-148,399,968 , GRCh37.p13 chr4: 149,321,120-149,321,120 NR3C2
    nsv5678091mobile element insertion2nstd211human GRCh38 chr4: 148,213,632-148,213,632 , GRCh37.p13 chr4: 149,134,783-149,134,783 NR3C2
    nsv5677967mobile element insertion1nstd211human GRCh38 chr4: 148,186,179-148,186,179 , GRCh37.p13 chr4: 149,107,330-149,107,330 NR3C2
    nsv5674586mobile element insertion1nstd211human GRCh38 chr4: 148,368,525-148,368,525 , GRCh37.p13 chr4: 149,289,677-149,289,677 NR3C2
    nsv5618078insertion1nstd207human GRCh38 chr4: 148,366,441-148,366,441 , GRCh37.p13 chr4: 149,287,593-149,287,593 NR3C2
    nsv5615623insertion1nstd207human GRCh38 chr4: 148,366,424-148,366,424 , GRCh37.p13 chr4: 149,287,576-149,287,576 NR3C2
    nsv5562962sequence alteration1nstd206human GRCh38 chr4: 148,077,189-148,077,292 , GRCh37.p13 chr4: 148,998,340-148,998,443 NR3C2
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5550433insertion1nstd206human GRCh38 chr4: 148,333,100-148,333,134 , GRCh37.p13 chr4: 149,254,252-149,254,286 NR3C2
    nsv5549357insertion1nstd206human GRCh38 chr4: 148,368,525-148,368,559 , GRCh37.p13 chr4: 149,289,677-149,289,711 NR3C2
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