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Items: 1 to 20 of 454

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4683389copy number variation1nstd102humanPathogenic GRCh37 chr2: 47,630,150-47,710,120 , GRCh38.p12 chr2: 47,403,011-47,482,981 MSH2
    nsv5381486copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr2: 47,630,252-47,710,088 , GRCh38.p12 chr2: 47,403,113-47,482,949 MSH2
    nsv4453903copy number variation1nstd102humanPathogenic GRCh38 chr2: 47,403,182-47,482,959 , GRCh37 chr2: 47,630,321-47,710,098 MSH2
    nsv7096663copy number variation1nstd102humanPathogenic GRCh37 chr2: 47,637,223-47,710,120 , GRCh38.p12 chr2: 47,410,084-47,482,981 MSH2
    nsv4453117copy number variation1nstd102humanPathogenic GRCh37 chr2: 47,637,223-47,710,098 , GRCh38 chr2: 47,410,084-47,482,959 MSH2
    nsv5673705copy number variation1nstd102humanPathogenic GRCh37 chr2: 47,635,062-47,705,668 , GRCh38.p12 chr2: 47,407,923-47,478,529 MSH2
    nsv4683937copy number variation1nstd102humanPathogenic GRCh37 chr2: 47,639,543-47,710,120 , GRCh38.p12 chr2: 47,412,404-47,482,981 MSH2
    nsv6311583copy number variation1nstd102humanPathogenic GRCh37 chr2: 47,630,252-47,693,967 , GRCh38.p12 chr2: 47,403,113-47,466,828 MSH2
    nsv6311410copy number variation1nstd102humanPathogenic GRCh37 chr2: 47,630,252-47,690,313 , GRCh38.p12 chr2: 47,403,113-47,463,174 MSH2
    nsv7096883copy number variation1nstd102humanPathogenic GRCh37 chr2: 47,635,530-47,693,957 , GRCh38.p12 chr2: 47,408,391-47,466,818 MSH2
    nsv5673709copy number variation1nstd102humanPathogenic GRCh37 chr2: 47,656,871-47,710,120 , GRCh38.p12 chr2: 47,429,732-47,482,981 MSH2
    nsv7096171copy number variation1nstd102humanPathogenic GRCh37 chr2: 47,656,871-47,708,020 , GRCh38.p12 chr2: 47,429,732-47,480,881 MSH2
    nsv4682368copy number variation1nstd102humanPathogenic GRCh37 chr2: 47,652,974-47,698,211 , GRCh38.p12 chr2: 47,425,835-47,471,072 MSH2
    nsv5673703copy number variation1nstd102humanPathogenic GRCh37 chr2: 47,630,252-47,672,806 , GRCh38.p12 chr2: 47,403,113-47,445,667 MSH2
    nsv6311411copy number variation1nstd102humanPathogenic GRCh37 chr2: 47,630,331-47,672,806 , GRCh38.p12 chr2: 47,403,192-47,445,667 MSH2
    nsv5673619copy number variation1nstd102humanPathogenic GRCh37 chr2: 47,669,476-47,710,120 , GRCh38.p12 chr2: 47,442,337-47,482,981 MSH2
    nsv4453500copy number variation1nstd102humanPathogenic GRCh38 chr2: 47,442,337-47,482,959 , GRCh37 chr2: 47,669,476-47,710,098 MSH2
    nsv5673546copy number variation1nstd102humanPathogenic GRCh37 chr2: 47,669,476-47,708,020 , GRCh38.p12 chr2: 47,442,337-47,480,881 MSH2
    nsv4683414copy number variation1nstd102humanPathogenic GRCh37 chr2: 47,672,677-47,710,098 , GRCh38.p12 chr2: 47,445,538-47,482,959 MSH2
    nsv4682995copy number variation1nstd102humanPathogenic GRCh37 chr2: 47,656,871-47,693,957 , GRCh38.p12 chr2: 47,429,732-47,466,818 MSH2
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