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Items: 1 to 20 of 226

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974464inversion1nstd209human GRCh38 chr19: 49,769,209-52,432,690 , GRCh37.p13 chr19: 50,272,466-52,935,943 , AP2A1, 172 more genes
    nsv5518385copy number variation1nstd206human GRCh38 chr19: 51,816,900-51,817,049 , GRCh37.p13 chr19: 52,320,153-52,320,302 FPR3, ZNF577
    nsv5515557copy number variation1nstd206human GRCh38 chr19: 51,768,552-52,114,487 , GRCh37.p13 chr19: 52,271,805-52,617,740 ZNF613, ZNF350-AS1, 17 more genes
    nsv5380300translocation1nstd200human GRCh38 chr19: 51,810,114-51,810,114 , GRCh38 chr19: 51,801,781-51,801,781 , GRCh37.p13 chr19: 52,313,367-52,313,367 , GRCh37.p13 chr19: 52,305,034-52,305,034 FPR3, ZNF577
    nsv5380299translocation1nstd200human GRCh38 chr19: 51,804,491-51,804,491 , GRCh38 chr19: 51,801,608-51,801,608 , GRCh37.p13 chr19: 52,304,861-52,304,861 , GRCh37.p13 chr19: 52,307,744-52,307,744 ZNF577, FPR3
    nsv5359905translocation1nstd200human GRCh38 chr19: 51,818,867-51,818,867 , GRCh38 chr19: 51,818,795-51,818,795 , GRCh37.p13 chr19: 52,322,048-52,322,048 , GRCh37.p13 chr19: 52,322,120-52,322,120 FPR3, ZNF577
    nsv5286855copy number variation1nstd204human GRCh38.p13 chr19: 51,818,001-51,821,300 , GRCh37.p13 chr19: 52,321,254-52,324,553 FPR3, ZNF577
    nsv5195337mobile element insertion1nstd203human GRCh38 chr19: 51,815,898-51,815,921 , GRCh37.p13 chr19: 52,319,151-52,319,174 ZNF577, FPR3
    nsv5024849copy number variation1nstd200human GRCh38 chr19: 51,821,897-51,839,808 , GRCh37.p13 chr19: 52,325,150-52,343,061 FPR3, ZNF577
    nsv5024848copy number variation1nstd200human GRCh38 chr19: 51,804,251-51,804,962 , GRCh37.p13 chr19: 52,307,504-52,308,215 ZNF577, FPR3
    nsv5024847copy number variation1nstd200human GRCh38 chr19: 51,768,552-52,114,487 , GRCh37.p13 chr19: 52,271,805-52,617,740 ZNF615, ZNF649-AS1, 17 more genes
    nsv5024846copy number variation1nstd200human GRCh38 chr19: 51,721,256-51,857,363 , GRCh37.p13 chr19: 52,224,509-52,360,616 FPR2, HAS1, 5 more genes
    nsv5021118copy number variation1nstd200human GRCh38 chr19: 51,813,289-51,814,518 , GRCh37.p13 chr19: 52,316,542-52,317,771 ZNF577, FPR3
    nsv5021117copy number variation1nstd200human GRCh38 chr19: 51,805,021-51,810,114 , GRCh37.p13 chr19: 52,308,274-52,313,367 FPR3, ZNF577
    nsv4865280copy number variation1nstd200human GRCh37 chr19: 52,271,805-52,617,740 , GRCh38.p12 chr19: 51,768,552-52,114,487 ZNF649, VN1R98P, 17 more genes
    nsv4865279copy number variation1nstd200human GRCh37 chr19: 52,224,509-52,360,616 , GRCh38.p12 chr19: 51,721,256-51,857,363 FPR1, LOC105372448, 5 more genes
    nsv4853438copy number variation1nstd200human GRCh37 chr19: 52,316,542-52,317,771 , GRCh38.p12 chr19: 51,813,289-51,814,518 FPR3, ZNF577
    nsv4729755copy number variation1nstd102humanPathogenic GRCh37 chr19: 48,463,931-57,095,254 , GRCh38.p12 chr19: 47,960,674-56,583,886 SIGLEC5, MED25, 574 more genes
    nsv4685764copy number variation1nstd102humannot provided GRCh37 chr19: 47,939,842-54,626,871 , GRCh38.p12 chr19: 47,436,585-54,071,460 SNAR-G1, IRF3, 453 more genes
    nsv4680470copy number variation1nstd189human GRCh37.p13 chr19: 52,276,523-52,620,956 , GRCh38.p12 chr19: 51,773,270-52,117,703 FPR3, ZNF432, 16 more genes
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