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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137701copy number variation1nstd102humanLikely pathogenic GRCh37 chr13: 28,669,064-31,367,407 , GRCh38.p12 chr13: 28,094,927-30,793,270 ALOX5AP, FLT1, 41 more genes
    nsv6112810copy number variation1nstd102humanPathogenic GRCh37 chr13: 28,925,153-34,061,696 , GRCh38.p12 chr13: 28,351,016-33,487,559 MTUS2, ALOX5AP, 70 more genes
    nsv5942649copy number variation1nstd209human GRCh38 chr13: 28,473,787-28,473,838 , GRCh37.p13 chr13: 29,047,924-29,047,975 FLT1
    nsv5936764copy number variation1nstd209human GRCh38 chr13: 28,377,409-28,377,474 , GRCh37.p13 chr13: 28,951,546-28,951,611 FLT1
    nsv5724661mobile element insertion1nstd211human GRCh38 chr13: 28,438,963-28,438,963 , GRCh37.p13 chr13: 29,013,100-29,013,100 FLT1
    nsv5702167mobile element insertion1nstd211human GRCh38 chr13: 28,461,281-28,461,281 , GRCh37.p13 chr13: 29,035,418-29,035,418 FLT1
    nsv5701908mobile element insertion2nstd211human GRCh38 chr13: 28,445,953-28,445,953 , GRCh37.p13 chr13: 29,020,090-29,020,090 FLT1
    nsv5697308mobile element insertion1nstd211human GRCh38 chr13: 28,369,867-28,369,867 , GRCh37.p13 chr13: 28,944,004-28,944,004 FLT1
    nsv5694477mobile element insertion1nstd211human GRCh38 chr13: 28,412,313-28,412,313 , GRCh37.p13 chr13: 28,986,450-28,986,450 FLT1
    nsv5653800insertion1nstd207human GRCh38 chr13: 28,453,025-28,453,025 , GRCh37.p13 chr13: 29,027,162-29,027,162 FLT1
    nsv5645923insertion1nstd207human GRCh38 chr13: 28,412,329-28,412,329 , GRCh37.p13 chr13: 28,986,466-28,986,466 FLT1
    nsv5594905copy number variation1nstd207human GRCh38 chr13: 28,473,757-28,473,812 , GRCh37.p13 chr13: 29,047,894-29,047,949 FLT1
    nsv5593376copy number variation1nstd207human GRCh38 chr13: 28,377,409-28,377,474 , GRCh37.p13 chr13: 28,951,546-28,951,611 FLT1
    nsv5593321copy number variation1nstd207human GRCh38 chr13: 28,453,027-28,453,077 , GRCh37.p13 chr13: 29,027,164-29,027,214 FLT1
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 RN7SL272P, DIAPH3, 1333 more genes
    nsv5555808mobile element insertion1nstd206human GRCh38 chr13: 28,438,963-28,439,014 , GRCh37.p13 chr13: 29,013,100-29,013,151 FLT1
    nsv5541519insertion1nstd206human GRCh38 chr13: 28,374,269-28,374,320 , GRCh37.p13 chr13: 28,948,406-28,948,457 FLT1
    nsv5513720copy number variation1nstd206human GRCh38 chr13: 28,411,676-28,415,929 , GRCh37.p13 chr13: 28,985,813-28,990,066 FLT1
    nsv5512617copy number variation1nstd206human GRCh38 chr13: 28,378,575-28,378,636 , GRCh37.p13 chr13: 28,952,712-28,952,773 FLT1
    nsv5511276copy number variation1nstd206human GRCh38 chr13: 28,451,410-28,451,725 , GRCh37.p13 chr13: 29,025,547-29,025,862 FLT1
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