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Items: 1 to 20 of 121

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098844copy number variation1nstd102humanUncertain significance GRCh37 chr2: 65,296,579-71,305,638 , GRCh38.p12 chr2: 65,069,445-71,078,508 SNRNP27, TEX261, 121 more genes
    nsv6677620copy number variation1nstd229human GRCh38 chr2: 68,646,701-68,650,300 , GRCh37.p13 chr2: 68,873,833-68,877,432 PROKR1
    nsv6672683copy number variation1nstd229human GRCh38 chr2: 68,650,850-68,660,225 , GRCh37.p13 chr2: 68,877,982-68,887,357 PROKR1
    nsv6671460copy number variation1nstd229human GRCh38 chr2: 68,654,201-68,673,500 , GRCh37.p13 chr2: 68,881,333-68,900,632 PROKR1
    nsv6667084copy number variation1nstd229human GRCh38 chr2: 68,656,401-68,668,100 , GRCh37.p13 chr2: 68,883,533-68,895,232 PROKR1
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CYP1B1-AS1, LOC107985771, 1649 more genes
    nsv6349503copy number variation1nstd223human GRCh38 chr2: 68,650,850-68,660,234 , GRCh37.p13 chr2: 68,877,982-68,887,366 PROKR1
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6314726copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196 ACTG2, ACYP2, 1713 more genes
    nsv6290436copy number variation1nstd102humanUncertain significance GRCh37 chr2: 68,791,921-68,938,872 , GRCh38.p12 chr2: 68,564,789-68,711,740 PROKR1, ARHGAP25, 2 more genes
    nsv6134545copy number variation2nstd213human GRCh37 chr2: 47,990,000-75,070,001 , GRCh38.p12 chr2: 47,762,861-74,842,874 ACTG2, ACYP2, 438 more genes
    nsv6134457copy number variation1nstd213human GRCh37 chr2: 38,410,000-75,540,001 , GRCh38.p12 chr2: 38,182,858-75,312,875 , ACTG2, 598 more genes
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5290437copy number variation1nstd204human GRCh38.p13 chr2: 68,652,457-68,667,784 , GRCh37.p13 chr2: 68,879,589-68,894,916 PROKR1
    nsv5213194copy number variation1nstd204human GRCh38.p13 chr2: 68,653,568-68,664,753 , GRCh37.p13 chr2: 68,880,700-68,891,885 PROKR1
    nsv5064009mobile element insertion1nstd203human GRCh38 chr2: 68,654,791-68,654,806 , GRCh37.p13 chr2: 68,881,923-68,881,938 PROKR1
    nsv4901755copy number variation1nstd200human GRCh38 chr2: 68,650,850-68,660,234 , GRCh37.p13 chr2: 68,877,982-68,887,366 PROKR1
    nsv4728523copy number variation1nstd102humanUncertain significance GRCh37 chr2: 68,559,849-68,869,517 , GRCh38.p12 chr2: 68,332,717-68,642,385 WDR4P2, PLEK, 7 more genes
    nsv4674632copy number variation1nstd102humanUncertain significance GRCh37 chr2: 68,652,771-68,957,105 , GRCh38.p12 chr2: 68,425,639-68,729,973 PROKR1, WDR4P2, 5 more genes
    nsv4584377copy number variation1nstd183human GRCh37 chr2: 68,880,811-68,903,422 , GRCh38.p12 chr2: 68,653,679-68,676,290 PROKR1
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