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Items: 1 to 20 of 209

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5937431copy number variation1nstd209human GRCh38 chr15: 41,238,133-41,239,858 , GRCh37.p13 chr15: 41,530,331-41,532,056 CHP1
    nsv5933461copy number variation1nstd209human GRCh38 chr15: 41,272,673-41,274,210 , GRCh37.p13 chr15: 41,564,871-41,566,408 CHP1
    nsv5932801copy number variation1nstd209human GRCh38 chr15: 41,227,538-41,229,214 , GRCh37.p13 chr15: 41,519,736-41,521,412 EXD1, CHP1
    nsv5861494copy number variation2nstd209human GRCh38 chr15: 41,280,519-41,282,044 , GRCh37.p13 chr15: 41,572,717-41,574,242 OIP5-AS1, CHP1
    nsv5854379copy number variation1nstd209human GRCh38 chr15: 41,238,146-41,239,845 , GRCh37.p13 chr15: 41,530,344-41,532,043 CHP1
    nsv5560202sequence alteration1nstd206human GRCh38 chr15: 41,268,831-41,268,832 , GRCh37.p13 chr15: 41,561,029-41,561,030 CHP1
    nsv5538529insertion1nstd206human GRCh38 chr15: 41,268,831-41,268,831 , GRCh37.p13 chr15: 41,561,029-41,561,029 CHP1
    nsv5512150copy number variation1nstd206human GRCh38 chr15: 41,246,216-41,246,283 , GRCh37.p13 chr15: 41,538,414-41,538,481 CHP1
    nsv5510116copy number variation1nstd206human GRCh38 chr15: 41,259,756-41,260,141 , GRCh37.p13 chr15: 41,551,954-41,552,339 CHP1
    nsv5505216copy number variation1nstd206human GRCh38 chr15: 41,280,615-41,280,962 , GRCh37.p13 chr15: 41,572,813-41,573,160 CHP1, OIP5-AS1
    nsv5498340copy number variation1nstd206human GRCh38 chr15: 41,227,087-41,229,215 , GRCh37.p13 chr15: 41,519,285-41,521,413 EXD1, CHP1
    nsv5496337copy number variation1nstd206human GRCh38 chr15: 41,273,826-41,279,152 , GRCh37.p13 chr15: 41,566,024-41,571,350 CHP1
    nsv5495974copy number variation1nstd206human GRCh38 chr15: 41,244,038-41,245,382 , GRCh37.p13 chr15: 41,536,236-41,537,580 CHP1
    nsv5495208copy number variation1nstd206human GRCh38 chr15: 41,246,416-41,247,053 , GRCh37.p13 chr15: 41,538,614-41,539,251 CHP1
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5380038translocation1nstd200human GRCh38 chr15: 41,368,667-41,368,667 , GRCh38 chr15: 41,261,476-41,261,476 , GRCh37.p13 chr15: 41,660,865-41,660,865 , GRCh37.p13 chr15: 41,553,674-41,553,674 NUSAP1, CHP1
    nsv5273546copy number variation1nstd204human GRCh38.p13 chr15: 41,100,101-41,426,600 , GRCh37.p13 chr15: 41,392,299-41,718,798 NUSAP1, RTF1, 9 more genes
    nsv5158833mobile element insertion1nstd203human GRCh38 chr15: 41,237,165-41,237,180 , GRCh37.p13 chr15: 41,529,363-41,529,378 CHP1
    nsv5155718mobile element insertion1nstd203human GRCh38 chr15: 41,268,831-41,268,849 , GRCh37.p13 chr15: 41,561,029-41,561,047 CHP1
    nsv5142366mobile element insertion1nstd203human GRCh38 chr15: 41,247,521-41,247,529 , GRCh37.p13 chr15: 41,539,719-41,539,727 CHP1
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