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Items: 1 to 20 of 162

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094244copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,915,399-22,005,055 , GRCh38.p12 chr14: 20,447,240-21,536,921 ARHGEF40, LOC105370398, 78 more genes
    nsv7076866inversion1nstd229human GRCh38 chr14: 20,744,118-20,754,046 , GRCh37.p13 chr14: 21,212,277-21,222,205 LOC107984671, EDDM3A
    nsv7066003inversion1nstd229human GRCh38 chr14: 20,733,234-20,733,781 , GRCh37.p13 chr14: 21,201,393-21,201,940 EDDM3A, EDDM3DP, 1 more genes
    nsv6952768copy number variation1nstd229human GRCh38 chr14: 20,684,552-20,730,337 , GRCh37.p13 chr14: 21,152,711-21,198,496 ANG, EDDM3A, 4 more genes
    nsv6948290copy number variation1nstd229human GRCh38 chr14: 20,735,383-20,747,241 , GRCh37.p13 chr14: 21,203,542-21,215,400 EDDM3DP, LOC107984671, 1 more genes
    nsv6946798copy number variation1nstd229human GRCh38 chr14: 20,555,975-20,753,534 , GRCh37.p13 chr14: 21,024,134-21,221,693 EDDM3A, RNASE9, 25 more genes
    nsv6942977copy number variation1nstd229human GRCh38 chr14: 20,736,346-20,737,042 , GRCh37.p13 chr14: 21,204,505-21,205,201 EDDM3A, LOC107984671
    nsv6940501copy number variation1nstd229human GRCh38 chr14: 20,715,860-20,725,118 , GRCh37.p13 chr14: 21,184,019-21,193,277 LOC107984671, RANBP20P, 1 more genes
    nsv6637318copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,690,196-23,114,522 , GRCh38.p12 chr14: 20,222,037-22,645,313 TRAJ21, TRAJ44, 239 more genes
    nsv6494617copy number variation1nstd223human GRCh38 chr14: 20,721,855-20,729,781 , GRCh37.p13 chr14: 21,190,014-21,197,940 RANBP20P, EDDM3A, 1 more genes
    nsv6487090copy number variation1nstd223human GRCh38 chr14: 20,743,564-20,743,949 , GRCh37.p13 chr14: 21,211,723-21,212,108 EDDM3A, LOC107984671
    nsv6486617copy number variation1nstd223human GRCh38 chr14: 20,723,001-20,723,800 , GRCh37.p13 chr14: 21,191,160-21,191,959 EDDM3A, RANBP20P
    nsv6482144copy number variation1nstd223human GRCh38 chr14: 20,746,151-20,768,582 , GRCh37.p13 chr14: 21,214,310-21,236,741 LOC107984671, EDDM3A, 1 more genes
    nsv6480973copy number variation1nstd223human GRCh38 chr14: 20,745,538-20,748,869 , GRCh37.p13 chr14: 21,213,697-21,217,028 EDDM3A, LOC107984671
    nsv6315513copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,672-47,481,203 , GRCh38.p12 chr14: 20,043,513-47,012,000 CDH24, KLHL33, 623 more genes
    nsv6314715copy number variation1nstd102humanPathogenic GRCh37 chr14: 21,162,263-50,713,602 , GRCh38.p12 chr14: 20,694,104-50,246,884 HNRNPC, FOXG1, 616 more genes
    nsv6290276copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 20,925,965-23,649,548 , GRCh38.p12 chr14: 20,457,806-23,180,339 ANG, APEX1, 255 more genes
    nsv6132583copy number variation1nstd213human GRCh37 chr14: 20,420,000-22,590,001 , GRCh38.p12 chr14: 19,951,841-22,122,043 HNRNPC, PNP, 157 more genes
    nsv6129746insertion1nstd186human GRCh37 chr14: 21,208,905-21,208,905 , GRCh38.p12 chr14: 20,740,746-20,740,746 LOC107984671, EDDM3A
    nsv5662510insertion1nstd207human GRCh38 chr14: 20,740,746-20,740,746 , GRCh37.p13 chr14: 21,208,905-21,208,905 LOC107984671, EDDM3A
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