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Items: 1 to 20 of 124

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5947717copy number variation1nstd209human GRCh38 chr22: 37,610,592-37,610,643 , GRCh37.p13 chr22: 38,006,599-38,006,650 GGA1
    nsv5547557copy number variation1nstd206human GRCh38 chr22: 37,611,904-37,612,217 , GRCh37.p13 chr22: 38,007,911-38,008,224 GGA1
    nsv5538835copy number variation1nstd206human GRCh38 chr22: 37,611,313-37,611,377 , GRCh37.p13 chr22: 38,007,320-38,007,384 GGA1
    nsv5536226copy number variation1nstd206human GRCh38 chr22: 37,612,261-37,612,568 , GRCh37.p13 chr22: 38,008,268-38,008,575 GGA1
    nsv5176378mobile element insertion1nstd203human GRCh38 chr22: 37,612,532-37,612,615 , GRCh37.p13 chr22: 38,008,539-38,008,622 GGA1
    nsv5174123mobile element insertion1nstd203human GRCh38 chr22: 37,612,530-37,612,615 , GRCh37.p13 chr22: 38,008,537-38,008,622 GGA1
    nsv5168454mobile element insertion1nstd203human GRCh38 chr22: 37,612,537-37,612,615 , GRCh37.p13 chr22: 38,008,544-38,008,622 GGA1
    nsv5161752mobile element insertion1nstd203human GRCh38 chr22: 37,612,493-37,612,537 , GRCh37.p13 chr22: 38,008,500-38,008,544 GGA1
    nsv5032407copy number variation1nstd200human GRCh38 chr22: 37,620,427-37,623,754 , GRCh37.p13 chr22: 38,016,434-38,019,761 GGA1
    nsv4729926copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,197,005-51,224,252 , GRCh38.p12 chr22: 16,367,190-50,785,824 FBXO7, GTSE1, 1084 more genes
    nsv4727972copy number variation1nstd197human GRCh38.p12 chr22: 37,632,406-37,632,711 , GRCh37 chr22: 38,028,413-38,028,718 GGA1
    nsv4676292copy number variation1nstd102humanPathogenic GRCh37 chr22: 30,654,764-51,197,838 , GRCh38.p12 chr22: 30,258,775-50,759,410 PDXP-DT, PDGFB, 550 more genes
    nsv4676116copy number variation1nstd102humanPathogenic GRCh37 chr22: 38,002,218-38,973,070 , GRCh38.p12 chr22: 37,606,211-38,577,065 CSNK1E, RN7SL704P, 43 more genes
    nsv4628489copy number variation1nstd183human GRCh37 chr22: 38,001,297-38,010,285 , GRCh38.p12 chr22: 37,605,290-37,614,278 GGA1
    nsv4457771copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,888,899-51,197,838 , GRCh38.p12 chr22: 16,408,173-50,759,410 IGLV3-27, XKR3, 1082 more genes
    nsv4342010sequence alteration1nstd166human GRCh37.p13 chr22: 37,991,705-38,015,430 , GRCh38.p12 chr22: 37,595,698-37,619,423 GGA1
    nsv4286511copy number variation1nstd166human GRCh37.p13 chr22: 38,019,057-38,024,526 , GRCh38.p12 chr22: 37,623,050-37,628,519 GGA1
    nsv4278013copy number variation1nstd166human GRCh37.p13 chr22: 37,381,892-38,500,309 , GRCh38.p12 chr22: 36,985,851-38,104,302 GGA1, GALR3, 46 more genes
    nsv3922128copy number variation1nstd102humanPathogenic GRCh37 chr22: 35,729,986-39,296,182 , NCBI36 chr22: 34,059,986-37,626,128 , GRCh38 chr22: 35,333,993-38,900,177 LOC102724378, CARD10, 120 more genes
    nsv3919881copy number variation1nstd102humanPathogenic GRCh37 chr22: 17,397,633-51,178,213 , GRCh38 chr22: 16,916,743-50,739,785 , NCBI36 chr22: 15,777,633-49,525,079 MIR12114, MIR6820, 1059 more genes
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