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Items: 1 to 20 of 458

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5904392copy number variation1nstd209human GRCh38 chr4: 184,652,938-184,653,045 , GRCh37.p13 chr4: 185,574,092-185,574,199 PRIMPOL
    nsv5685117mobile element insertion2nstd211human GRCh38 chr4: 184,684,539-184,684,539 , GRCh37.p13 chr4: 185,605,693-185,605,693 PRIMPOL
    nsv5642154insertion1nstd207human GRCh38 chr4: 184,676,222-184,676,222 , GRCh37.p13 chr4: 185,597,376-185,597,376 PRIMPOL
    nsv5640974insertion1nstd207human GRCh38 chr4: 184,676,460-184,676,460 , GRCh37.p13 chr4: 185,597,614-185,597,614 PRIMPOL
    nsv5637466insertion1nstd207human GRCh38 chr4: 184,676,176-184,676,176 , GRCh37.p13 chr4: 185,597,330-185,597,330 PRIMPOL
    nsv5630364insertion1nstd207human GRCh38 chr4: 184,689,083-184,689,083 , GRCh37.p13 chr4: 185,610,237-185,610,237 PRIMPOL
    nsv5627508insertion1nstd207human GRCh38 chr4: 184,676,387-184,676,387 , GRCh37.p13 chr4: 185,597,541-185,597,541 PRIMPOL
    nsv5581180copy number variation1nstd207human GRCh38 chr4: 184,676,453-184,676,680 , GRCh37.p13 chr4: 185,597,607-185,597,834 PRIMPOL
    nsv5573180copy number variation1nstd207human GRCh38 chr4: 184,676,431-184,676,511 , GRCh37.p13 chr4: 185,597,585-185,597,665 PRIMPOL
    nsv5566427copy number variation1nstd207human GRCh38 chr4: 184,652,937-184,653,038 , GRCh37.p13 chr4: 185,574,091-185,574,192 PRIMPOL
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5535315insertion1nstd206human GRCh38 chr4: 184,653,664-184,653,702 , GRCh37.p13 chr4: 185,574,818-185,574,856 PRIMPOL
    nsv5457945copy number variation1nstd206human GRCh38 chr4: 184,668,165-184,673,497 , GRCh37.p13 chr4: 185,589,319-185,594,651 PRIMPOL
    nsv5454803copy number variation1nstd206human GRCh38 chr4: 184,212,885-185,009,149 , GRCh37.p13 chr4: 185,134,038-185,930,303 , RPL6P16, 22 more genes
    nsv5401798mobile element insertion1nstd206human GRCh38 chr4: 184,684,539-184,684,590 , GRCh37.p13 chr4: 185,605,693-185,605,744 PRIMPOL
    nsv5228365copy number variation1nstd204human GRCh38.p13 chr4: 184,648,940-184,651,273 , GRCh37.p13 chr4: 185,570,094-185,572,427 CASP3, PRIMPOL
    nsv5221553copy number variation1nstd204human GRCh38.p13 chr4: 184,075,301-184,744,600 , GRCh37.p13 chr4: 184,996,454-185,665,754 , LINC02365, 14 more genes
    nsv5200366copy number variation1nstd102humanLikely pathogenic GRCh37 chr4: 179,554,876-190,916,678 , GRCh38.p12 chr4: 178,633,722-189,995,523 SLC25A4, CASP3, 151 more genes
    nsv5091565mobile element insertion1nstd203human GRCh38 chr4: 184,653,651-184,653,664 , GRCh37.p13 chr4: 185,574,805-185,574,818 PRIMPOL
    nsv4944132copy number variation1nstd200human GRCh38 chr4: 184,678,030-184,678,519 , GRCh37.p13 chr4: 185,599,184-185,599,673 PRIMPOL
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