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Items: 1 to 20 of 147

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5975412insertion1nstd209human GRCh38 chr20: 25,678,468-25,678,468 , GRCh37.p13 chr20: 25,659,104-25,659,104 ZNF337, ZNF337-AS1
    nsv5957622copy number variation1nstd209human GRCh38 chr20: 25,676,302-25,676,553 , GRCh37.p13 chr20: 25,656,938-25,657,189 ZNF337-AS1, ZNF337
    nsv5328014copy number variation1nstd204human GRCh38.p13 chr20: 25,516,433-25,858,450 , GRCh37.p13 chr20: 25,497,069-25,839,086 LOC107985400, LOC105372582, 12 more genes
    nsv5324431copy number variation1nstd204human GRCh37.p13 chr20: 25,656,027-25,656,187 , GRCh38.p13 chr20: 25,675,391-25,675,551 ZNF337-AS1, ZNF337
    nsv5025242copy number variation1nstd200human GRCh38 chr20: 25,516,440-25,858,448 , GRCh37.p13 chr20: 25,497,076-25,839,084 BSNDP1, RN7SL594P, 12 more genes
    nsv5021853copy number variation1nstd200human GRCh38 chr20: 25,675,400-25,675,543 , GRCh37.p13 chr20: 25,656,036-25,656,179 ZNF337, ZNF337-AS1
    nsv5021852copy number variation1nstd200human GRCh38 chr20: 25,665,035-25,718,953 , GRCh37.p13 chr20: 25,645,671-25,699,589 LOC107985400, MED28P7, 2 more genes
    nsv5021851copy number variation1nstd200human GRCh38 chr20: 25,663,067-25,680,038 , GRCh37.p13 chr20: 25,643,703-25,660,674 ZNF337, ZNF337-AS1, 1 more genes
    nsv4868537copy number variation1nstd200human GRCh37 chr20: 25,664,329-25,665,060 , GRCh38.p12 chr20: 25,683,693-25,684,424 ZNF337
    nsv4868536copy number variation1nstd200human GRCh37 chr20: 25,656,036-25,656,179 , GRCh38.p12 chr20: 25,675,400-25,675,543 ZNF337, ZNF337-AS1
    nsv4865508copy number variation1nstd200human GRCh37 chr20: 25,497,076-25,839,084 , GRCh38.p12 chr20: 25,516,440-25,858,448 FAM182B, VN1R108P, 12 more genes
    nsv4862419copy number variation1nstd200human GRCh37 chr20: 25,645,671-25,699,589 , GRCh38.p12 chr20: 25,665,035-25,718,953 MED28P7, LOC107985400, 2 more genes
    nsv4729757copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 19,750,804-30,479,077 , GRCh38.p12 chr20: 19,770,160-31,891,274 BCL2L1, CD24P3, 222 more genes
    nsv4679352copy number variation1nstd189human GRCh37.p13 chr20: 25,441,848-26,305,579 , GRCh38.p12 chr20: 25,461,212-26,324,943 NINL, ZNF337, 20 more genes
    nsv4630374copy number variation1nstd183human GRCh37 chr20: 25,665,467-25,754,850 , GRCh38.p12 chr20: 25,684,831-25,774,214 ZNF337, LOC107985400, 3 more genes
    nsv4571500insertion1nstd166human GRCh37.p13 chr20: 25,659,103-25,659,103 , GRCh38.p12 chr20: 25,678,467-25,678,467 ZNF337-AS1, ZNF337
    nsv4457685copy number variation2nstd102humanUncertain significance GRCh37 chr20: 25,496,752-25,657,484 , GRCh38.p12 chr20: 25,516,116-25,676,848 ZNF337-AS1, RN7SL594P, 5 more genes
    nsv4420325copy number variation1nstd174human GRCh37 chr20: 25,662,941-25,744,711 , GRCh38.p12 chr20: 25,682,305-25,764,075 LOC107985400, VN1R108P, 3 more genes
    nsv4366602copy number variation1nstd173human GRCh37 chr20: 25,665,135-25,744,722 , GRCh38.p12 chr20: 25,684,499-25,764,086 LOC105372582, ZNF337, 3 more genes
    nsv4349190copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,568-26,305,479 , GRCh38.p12 chr20: 80,927-26,324,843 LOC105372582, LOC101929937, 473 more genes
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