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Items: 1 to 20 of 410

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5960383insertion1nstd209human GRCh38 chr4: 77,819,049-77,819,049 , GRCh37.p13 chr4: 78,740,203-78,740,203 CNOT6L
    nsv5722205mobile element insertion1nstd211human GRCh38 chr4: 77,724,858-77,724,858 , GRCh37.p13 chr4: 78,646,012-78,646,012 CNOT6L
    nsv5721895mobile element insertion1nstd211human GRCh38 chr4: 77,786,894-77,786,894 , GRCh37.p13 chr4: 78,708,048-78,708,048 CNOT6L
    nsv5715175mobile element insertion2nstd211human GRCh38 chr4: 77,756,633-77,756,633 , GRCh37.p13 chr4: 78,677,787-78,677,787 CNOT6L
    nsv5676221mobile element insertion2nstd211human GRCh38 chr4: 77,754,913-77,754,913 , GRCh37.p13 chr4: 78,676,067-78,676,067 CNOT6L
    nsv5617077insertion2nstd207human GRCh38 chr4: 77,819,049-77,819,049 , GRCh37.p13 chr4: 78,740,203-78,740,203 CNOT6L
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5557039mobile element insertion1nstd206human GRCh38 chr4: 77,786,894-77,786,945 , GRCh37.p13 chr4: 78,708,048-78,708,099 CNOT6L
    nsv5547030insertion1nstd206human GRCh38 chr4: 68,996,170-113,894,177 , GRCh37.p13 chr4: 69,861,888-114,815,333 , MIR548AH, 616 more genes
    nsv5541190insertion1nstd206human GRCh38 chr4: 77,721,980-77,722,016 , GRCh37.p13 chr4: 78,643,134-78,643,170 CNOT6L
    nsv5469177copy number variation1nstd206human GRCh38 chr4: 77,818,731-77,818,937 , GRCh37.p13 chr4: 78,739,885-78,740,091 CNOT6L
    nsv5464711copy number variation1nstd206human GRCh38 chr4: 77,781,683-77,788,972 , GRCh37.p13 chr4: 78,702,837-78,710,126 CNOT6L
    nsv5455524copy number variation1nstd206human GRCh38 chr4: 77,819,170-77,819,879 , GRCh37.p13 chr4: 78,740,324-78,741,033 CNOT6L
    nsv5454883copy number variation1nstd206human GRCh38 chr4: 77,804,614-77,804,712 , GRCh37.p13 chr4: 78,725,768-78,725,866 CNOT6L
    nsv5346758translocation1nstd200human GRCh38 chr4: 77,712,470-77,712,470 , GRCh38 chr4: 77,712,395-77,712,395 , GRCh37.p13 chr4: 78,633,549-78,633,549 , GRCh37.p13 chr4: 78,633,624-78,633,624 CNOT6L
    nsv5329712translocation1nstd200human GRCh37 chr4: 78,633,624-78,633,624 , GRCh37 chr4: 78,633,549-78,633,549 , GRCh38.p12 chr4: 77,712,395-77,712,395 , GRCh38.p12 chr4: 77,712,470-77,712,470 CNOT6L
    nsv5316344copy number variation1nstd204human GRCh38.p13 chr4: 77,775,872-77,776,020 , GRCh37.p13 chr4: 78,697,026-78,697,174 CNOT6L
    nsv5174706mobile element insertion1nstd203human GRCh38 chr4: 77,810,817-77,810,832 , GRCh37.p13 chr4: 78,731,971-78,731,986 CNOT6L
    nsv5099049mobile element insertion1nstd203human GRCh38 chr4: 77,716,111-77,716,121 , GRCh37.p13 chr4: 78,637,265-78,637,275 CNOT6L
    nsv5085642mobile element insertion1nstd203human GRCh38 chr4: 77,794,150-77,794,200 , GRCh37.p13 chr4: 78,715,304-78,715,354 CNOT6L
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