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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112761copy number variation1nstd102humanPathogenic GRCh37 chr4: 69,671-29,702,595 , GRCh38.p12 chr4: 69,779-29,700,973 LOC101928306, PDE6B-AS1, 460 more genes
    nsv6112747copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,598-18,912,995 , GRCh38.p12 chr4: 68,706-18,911,372 GPR78, LOC105374510, 362 more genes
    nsv5900136copy number variation1nstd209human GRCh38 chr4: 2,161,908-2,161,957 , GRCh37.p13 chr4: 2,163,635-2,163,684 POLN
    nsv5898636copy number variation1nstd209human GRCh38 chr4: 2,231,846-2,235,811 , GRCh37.p13 chr4: 2,233,573-2,237,538 HAUS3, POLN, 1 more genes
    nsv5898417copy number variation1nstd209human GRCh38 chr4: 2,070,061-2,070,282 , GRCh37.p13 chr4: 2,071,788-2,072,009 POLN
    nsv5890589copy number variation1nstd209human GRCh38 chr4: 2,097,337-2,097,637 , GRCh37.p13 chr4: 2,099,064-2,099,364 POLN
    nsv5839511copy number variation1nstd209human GRCh38 chr4: 2,231,825-2,235,844 , GRCh37.p13 chr4: 2,233,552-2,237,571 COX6B1P5, POLN, 1 more genes
    nsv5690817mobile element insertion2nstd211human GRCh38 chr4: 2,217,631-2,217,631 , GRCh37.p13 chr4: 2,219,358-2,219,358 POLN
    nsv5689705mobile element insertion1nstd211human GRCh38 chr4: 2,199,969-2,199,969 , GRCh37.p13 chr4: 2,201,696-2,201,696 POLN
    nsv5688744mobile element insertion1nstd211human GRCh38 chr4: 2,228,244-2,228,244 , GRCh37.p13 chr4: 2,229,971-2,229,971 HAUS3, POLN
    nsv5686809mobile element insertion2nstd211human GRCh38 chr4: 2,226,630-2,226,630 , GRCh37.p13 chr4: 2,228,357-2,228,357 HAUS3, POLN
    nsv5673743copy number variation1nstd102humanPathogenic GRCh37 chr4: 2,200,251-5,710,240 , GRCh38.p12 chr4: 2,198,524-5,708,513 ZFYVE28, LINC01587, 81 more genes
    nsv5673649copy number variation1nstd102humanPathogenic GRCh37 chr4: 1,619,775-2,181,192 , GRCh38.p12 chr4: 1,618,048-2,179,465 NSD2, TMEM129, 15 more genes
    nsv5610880insertion1nstd207human GRCh38 chr4: 2,221,917-2,221,917 , GRCh37.p13 chr4: 2,223,644-2,223,644 POLN
    nsv5610801insertion2nstd207human GRCh38 chr4: 2,080,410-2,080,410 , GRCh37.p13 chr4: 2,082,137-2,082,137 POLN
    nsv5410051mobile element insertion1nstd206human GRCh38 chr4: 2,217,631-2,217,682 , GRCh37.p13 chr4: 2,219,358-2,219,409 POLN
    nsv5404690mobile element insertion1nstd206human GRCh38 chr4: 2,199,969-2,200,020 , GRCh37.p13 chr4: 2,201,696-2,201,747 POLN
    nsv5401030mobile element insertion1nstd206human GRCh38 chr4: 2,190,377-2,190,428 , GRCh37.p13 chr4: 2,192,104-2,192,155 POLN
    nsv5399376mobile element insertion1nstd206human GRCh38 chr4: 2,226,630-2,226,681 , GRCh37.p13 chr4: 2,228,357-2,228,408 POLN, HAUS3
    nsv5381775copy number variation1nstd102humanPathogenic GRCh37 chr4: 388,344-3,872,380 , GRCh38.p12 chr4: 394,555-3,870,653 RN7SL671P, HTT-AS, 96 more genes
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