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Items: 1 to 20 of 164

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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
    nsv7072428inversion1nstd229human GRCh38 chr19: 19,651,377-19,719,546 , GRCh37.p13 chr19: 19,762,186-19,830,355 ATP13A1, ZNF14, 1 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
    nsv7005241copy number variation1nstd229human GRCh38 chr19: 19,666,594-19,674,467 , GRCh37.p13 chr19: 19,777,403-19,785,276 ZNF101
    nsv7000136copy number variation1nstd229human GRCh38 chr19: 19,683,057-19,764,012 , GRCh37.p13 chr19: 19,793,866-19,874,821 LINC00663, ZNF101, 3 more genes
    nsv6624683copy number variation1nstd224human GRCh37 chr19: 19,788,795-19,810,078 , GRCh38.p12 chr19: 19,677,986-19,699,269 ZNF101
    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
    nsv6598222inversion1nstd223human GRCh38 chr19: 19,670,903-19,671,638 , GRCh37.p13 chr19: 19,781,712-19,782,447 ZNF101
    nsv6518804copy number variation1nstd223human GRCh38 chr19: 19,673,989-19,691,063 , GRCh37.p13 chr19: 19,784,798-19,801,872 ZNF101
    nsv6518744copy number variation1nstd223human GRCh38 chr19: 19,664,625-19,667,280 , GRCh37.p13 chr19: 19,775,434-19,778,089 ZNF101
    nsv6515614copy number variation1nstd223human GRCh38 chr19: 19,666,120-19,680,030 , GRCh37.p13 chr19: 19,776,929-19,790,839 ZNF101
    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
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