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Items: 1 to 20 of 110

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7060212inversion1nstd229human GRCh38 chr19: 19,578,137-19,720,249 , GRCh37.p13 chr19: 19,688,946-19,831,058 ZNF14, PBX4, 5 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
    nsv7009173copy number variation1nstd229human GRCh38 chr19: 19,578,101-19,651,400 , GRCh37.p13 chr19: 19,688,910-19,762,209 ATP13A1, LPAR2, 3 more genes
    nsv6624637copy number variation1nstd224human GRCh37 chr19: 19,692,579-19,906,362 , GRCh38.p12 chr19: 19,581,770-19,795,553 GMIP, LOC101060187, 10 more genes
    nsv6599077inversion1nstd223human GRCh38 chr19: 12,342,953-19,691,233 , GRCh37.p13 chr19: 12,453,767-19,802,042 GET3, BST2, 314 more genes
    nsv6526834copy number variation1nstd223human GRCh38 chr19: 19,625,027-19,641,289 , GRCh37.p13 chr19: 19,735,836-19,752,098 GMIP, LPAR2
    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
    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
    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
    nsv5299782copy number variation1nstd204human GRCh38.p13 chr19: 18,706,301-19,688,800 , GRCh37.p13 chr19: 18,817,111-19,799,609 , HOMER3-AS1, 37 more genes
    nsv5041043inversion1nstd200human GRCh38 chr19: 11,963,569-20,150,886 , GRCh37.p13 chr19: 12,074,384-20,193,556 , USE1, 369 more genes
    nsv5019486copy number variation1nstd200human GRCh38 chr19: 19,639,028-19,643,418 , GRCh37.p13 chr19: 19,749,837-19,754,227 ATP13A1, GMIP
    nsv5019485copy number variation1nstd200human GRCh38 chr19: 19,622,416-19,631,256 , GRCh37.p13 chr19: 19,733,225-19,742,065 LPAR2, GMIP
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