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Items: 1 to 20 of 536

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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
    nsv5906076copy number variation1nstd209human GRCh38 chr4: 146,760,758-146,760,820 , GRCh37.p13 chr4: 147,681,910-147,681,972 TTC29
    nsv5896345copy number variation1nstd209human GRCh38 chr4: 146,809,025-146,809,937 , GRCh37.p13 chr4: 147,730,177-147,731,089 TTC29
    nsv5896233copy number variation1nstd209human GRCh38 chr4: 146,190,128-146,855,608 , GRCh37.p13 chr4: 147,111,280-147,776,760 POU4F2, LSM6, 7 more genes
    nsv5894974copy number variation1nstd209human GRCh38 chr4: 146,944,375-146,945,443 , GRCh37.p13 chr4: 147,865,527-147,866,595 TTC29, LOC105377473
    nsv5888885copy number variation1nstd209human GRCh38 chr4: 146,728,761-146,728,824 , GRCh37.p13 chr4: 147,649,913-147,649,976 TTC29
    nsv5837739copy number variation1nstd209human GRCh38 chr4: 146,783,318-146,801,633 , GRCh37.p13 chr4: 147,704,470-147,722,785 TTC29
    nsv5837738copy number variation1nstd209human GRCh38 chr4: 146,677,523-146,706,579 , GRCh37.p13 chr4: 147,598,675-147,627,731 TTC29
    nsv5729594mobile element insertion1nstd211human GRCh38 chr4: 146,918,283-146,918,283 , GRCh37.p13 chr4: 147,839,435-147,839,435 TTC29
    nsv5728511mobile element insertion1nstd211human GRCh38 chr4: 146,945,235-146,945,235 , GRCh37.p13 chr4: 147,866,387-147,866,387 LOC105377473, TTC29
    nsv5728344mobile element insertion1nstd211human GRCh38 chr4: 146,832,800-146,832,800 , GRCh37.p13 chr4: 147,753,952-147,753,952 TTC29, LOC105377474
    nsv5724887mobile element insertion1nstd211human GRCh38 chr4: 146,902,693-146,902,693 , GRCh37.p13 chr4: 147,823,845-147,823,845 TTC29
    nsv5716699mobile element insertion1nstd211human GRCh38 chr4: 146,820,060-146,820,060 , GRCh37.p13 chr4: 147,741,212-147,741,212 TTC29
    nsv5692904mobile element insertion2nstd211human GRCh38 chr4: 146,881,892-146,881,892 , GRCh37.p13 chr4: 147,803,044-147,803,044 TTC29
    nsv5689040mobile element insertion2nstd211human GRCh38 chr4: 146,826,770-146,826,770 , GRCh37.p13 chr4: 147,747,922-147,747,922 TTC29
    nsv5688705mobile element insertion2nstd211human GRCh38 chr4: 146,936,897-146,936,897 , GRCh37.p13 chr4: 147,858,049-147,858,049 TTC29, LOC105377473
    nsv5616668insertion1nstd207human GRCh38 chr4: 146,728,815-146,728,815 , GRCh37.p13 chr4: 147,649,967-147,649,967 TTC29
    nsv5572975copy number variation1nstd207human GRCh38 chr4: 146,809,025-146,809,937 , GRCh37.p13 chr4: 147,730,177-147,731,089 TTC29
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5557859mobile element insertion1nstd206human GRCh38 chr4: 146,918,283-146,918,334 , GRCh37.p13 chr4: 147,839,435-147,839,486 TTC29
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