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Items: 1 to 20 of 247

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5935173copy number variation1nstd209human GRCh38 chr17: 75,698,497-75,698,595 , GRCh37.p13 chr17: 73,694,577-73,694,675 SAP30BP
    nsv5532284copy number variation1nstd206human GRCh38 chr17: 75,677,505-75,685,026 , GRCh37.p13 chr17: 73,673,585-73,681,106 SAP30BP
    nsv5514202copy number variation1nstd206human GRCh38 chr17: 75,682,821-75,686,333 , GRCh37.p13 chr17: 73,678,901-73,682,413 SAP30BP
    nsv5293343copy number variation1nstd204human GRCh38.p13 chr17: 74,899,101-76,684,700 , GRCh37.p13 chr17: 72,895,199-74,680,782 , RNU6-24P, 92 more genes
    nsv5285796copy number variation1nstd204human GRCh37.p13 chr17: 73,542,682-73,669,280 , GRCh38.p13 chr17: 75,546,601-75,673,200 LLGL2, RECQL5, 5 more genes
    nsv5282319copy number variation1nstd204human GRCh38.p13 chr17: 75,609,901-75,917,300 , GRCh37.p13 chr17: 73,605,982-73,913,381 ITGB4, TRIM65, 15 more genes
    nsv5146069mobile element insertion1nstd203human GRCh38 chr17: 75,674,690-75,674,725 , GRCh37.p13 chr17: 73,670,770-73,670,805 SAP30BP
    nsv5016705copy number variation1nstd200human GRCh38 chr17: 75,677,501-75,685,026 , GRCh37.p13 chr17: 73,673,581-73,681,106 SAP30BP
    nsv5016703copy number variation1nstd200human GRCh38 chr17: 75,659,157-75,682,226 , GRCh37.p13 chr17: 73,655,237-73,678,306 RECQL5, LOC107985013, 1 more genes
    nsv5014025copy number variation1nstd200human GRCh38 chr17: 75,682,364-75,683,380 , GRCh37.p13 chr17: 73,678,444-73,679,460 SAP30BP
    nsv4858987copy number variation1nstd200human GRCh37 chr17: 73,673,585-73,681,106 , GRCh38.p12 chr17: 75,677,505-75,685,026 SAP30BP
    nsv4854396copy number variation1nstd200human GRCh37 chr17: 73,669,578-73,685,780 , GRCh38.p12 chr17: 75,673,498-75,689,700 SAP30BP
    nsv4854394copy number variation1nstd200human GRCh37 chr17: 73,511,580-73,714,116 , GRCh38.p12 chr17: 75,515,499-75,718,036 , CASKIN2, 8 more genes
    nsv4676104copy number variation1nstd102humanPathogenic GRCh37 chr17: 73,261,871-78,608,763 , GRCh38.p12 chr17: 75,265,790-80,634,963 LLGL2, TSEN54, 165 more genes
    nsv4628995copy number variation1nstd183human GRCh37 chr17: 73,217,773-73,774,243 , GRCh38.p12 chr17: 75,221,678-75,778,162 , LOC107985013, 23 more genes
    nsv4574621mobile element insertion1nstd166human GRCh37.p13 chr17: 73,662,465-73,662,465 , GRCh38.p12 chr17: 75,666,385-75,666,385 SAP30BP, RECQL5
    nsv4569850inversion1nstd166human GRCh37.p13 chr17: 73,573,022-73,825,589 , GRCh38.p12 chr17: 75,576,941-75,829,508 GALK1, H3-3B, 10 more genes
    nsv4552778insertion1nstd166human GRCh37.p13 chr17: 73,664,913-73,664,913 , GRCh38.p12 chr17: 75,668,833-75,668,833 SAP30BP
    nsv4457679copy number variation1nstd102humanUncertain significance GRCh37 chr17: 73,596,063-73,959,466 , GRCh38.p12 chr17: 75,599,982-75,963,385 MIR4738, RECQL5, 16 more genes
    nsv4457646copy number variation1nstd102humanPathogenic GRCh37 chr17: 62,778,720-81,041,938 , GRCh38.p12 chr17: 64,782,602-83,084,062 LOC107985089, ARSG, 448 more genes
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