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Items: 1 to 20 of 130

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146904insertion1nstd232human GRCh37.p13 chr19: 19,637,071-19,637,071 , GRCh38.p12 chr19: 19,526,262-19,526,262 NDUFA13
    nsv7144353insertion1nstd232human GRCh37.p13 chr19: 19,627,141-19,627,141 , GRCh38.p12 chr19: 19,516,332-19,516,332 NDUFA13
    nsv7142371insertion1nstd232human GRCh37.p13 chr19: 19,632,427-19,632,427 , GRCh38.p12 chr19: 19,521,618-19,521,618 NDUFA13
    nsv7076266inversion1nstd229human GRCh38 chr19: 19,130,894-20,543,167 , GRCh37.p13 chr19: 19,241,703-20,193,556 ZNF101, GATAD2A, 65 more genes
    nsv7065580inversion1nstd229human GRCh38 chr19: 11,963,576-20,150,892 , GRCh37.p13 chr19: 12,074,391-20,193,556 CYP4F24P, CYP4F2, 359 more genes
    nsv7060542inversion1nstd229human GRCh38 chr19: 12,342,956-19,691,233 , GRCh37.p13 chr19: 12,453,770-19,802,042 DDX39A, KCNN1, 314 more genes
    nsv7059139inversion1nstd229human GRCh38 chr19: 12,641,624-19,910,103 , GRCh37.p13 chr19: 12,752,438-20,020,912 NR2F6, ISCA1P5, 307 more genes
    nsv7013800copy number variation1nstd229human GRCh38 chr19: 19,512,572-19,936,031 , GRCh37.p13 chr19: 19,623,381-20,046,840 ZNF506, PBX4, 19 more genes
    nsv7000823copy number variation1nstd229human GRCh38 chr19: 19,522,358-19,522,439 , GRCh37.p13 chr19: 19,633,167-19,633,248 NDUFA13
    nsv6599077inversion1nstd223human GRCh38 chr19: 12,342,953-19,691,233 , GRCh37.p13 chr19: 12,453,767-19,802,042 GET3, BST2, 314 more genes
    nsv6524383copy number variation1nstd223human GRCh38 chr19: 19,521,042-19,523,740 , GRCh37.p13 chr19: 19,631,851-19,634,549 NDUFA13
    nsv6516005copy number variation1nstd223human GRCh38 chr19: 19,518,498-19,571,449 , GRCh37.p13 chr19: 19,629,307-19,682,258 YJEFN3, CILP2, 2 more genes
    nsv6290300copy number variation1nstd102humanPathogenic GRCh37 chr19: 19,546,923-41,313,229 , GRCh38.p12 chr19: 19,436,114-40,807,324 ZNF420, LOC105372330, 574 more genes
    nsv6209946copy number variation1nstd214human GRCh38 chr19: 19,519,972-19,520,032 , GRCh37.p13 chr19: 19,630,781-19,630,841 NDUFA13
    nsv6133402copy number variation1nstd213human GRCh37 chr19: 19,150,000-24,140,001 , GRCh38.p12 chr19: 19,039,191-23,957,199 , NCAN, 199 more genes
    nsv6133401copy number variation1nstd213human GRCh37 chr19: 19,110,000-24,140,001 , GRCh38.p12 chr19: 18,999,191-23,957,199 , NCAN, 200 more genes
    nsv6133400copy number variation1nstd213human GRCh37 chr19: 18,720,000-20,740,001 , GRCh38.p12 chr19: 18,609,190-20,557,195 COMP, NCAN, 81 more genes
    nsv6111867insertion1nstd212human GRCh38 chr19: 19,521,989-19,521,989 , GRCh37.p13 chr19: 19,632,798-19,632,798 NDUFA13
    nsv6102553inversion1nstd212human GRCh38 chr19: 18,724,785-21,720,303 , GRCh37.p13 chr19: 18,835,595-21,903,105 , COMP, 127 more genes
    nsv5974799inversion1nstd209human GRCh38 chr19: 12,342,936-19,691,231 , GRCh37.p13 chr19: 12,453,750-19,802,040 , GET3, 322 more genes
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