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Items: 1 to 20 of 263

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5937211copy number variation1nstd209human GRCh38 chr19: 20,029,419-20,031,758 , GRCh37.p13 chr19: 20,140,228-20,142,567 ZNF682, LOC105372308
    nsv5882788copy number variation1nstd209human GRCh38 chr19: 20,029,528-20,031,827 , GRCh37.p13 chr19: 20,140,337-20,142,636 LOC101928960, LOC105372308, 1 more genes
    nsv5716685mobile element insertion1nstd211human GRCh38 chr19: 20,021,487-20,021,487 , GRCh37.p13 chr19: 20,132,296-20,132,296 ZNF682
    nsv5697863mobile element insertion2nstd211human GRCh38 chr19: 20,030,910-20,030,910 , GRCh37.p13 chr19: 20,141,719-20,141,719 ZNF682, LOC105372308
    nsv5523542copy number variation1nstd206human GRCh38 chr19: 20,029,451-20,031,759 , GRCh37.p13 chr19: 20,140,260-20,142,568 LOC105372308, ZNF682
    nsv5520420copy number variation1nstd206human GRCh38 chr19: 20,036,575-20,036,932 , GRCh37.p13 chr19: 20,147,384-20,147,741 ZNF682
    nsv5516890copy number variation1nstd206human GRCh38 chr19: 20,033,614-20,041,034 , GRCh37.p13 chr19: 20,144,423-20,151,843 ZNF682, LOC105372309, 1 more genes
    nsv5425162mobile element insertion1nstd206human GRCh38 chr19: 20,030,910-20,030,961 , GRCh37.p13 chr19: 20,141,719-20,141,770 ZNF682, LOC105372308
    nsv5176429mobile element insertion1nstd203human GRCh38 chr19: 20,003,190-20,003,220 , GRCh37.p13 chr19: 20,113,999-20,114,029 ZNF682, BNIP3P12
    nsv5167336mobile element insertion1nstd203human GRCh38 chr19: 20,003,144-20,003,190 , GRCh37.p13 chr19: 20,113,953-20,113,999 BNIP3P12, ZNF682
    nsv5041043inversion1nstd200human GRCh38 chr19: 11,963,569-20,150,886 , GRCh37.p13 chr19: 12,074,384-20,193,556 , USE1, 369 more genes
    nsv5019518copy number variation1nstd200human GRCh38 chr19: 20,033,844-20,035,888 , GRCh37.p13 chr19: 20,144,653-20,146,697 ZNF682, LOC101928960
    nsv5019517copy number variation1nstd200human GRCh38 chr19: 20,031,567-20,032,303 , GRCh37.p13 chr19: 20,142,376-20,143,112 LOC101928960, LOC105372308, 1 more genes
    nsv5019516copy number variation1nstd200human GRCh38 chr19: 20,029,451-20,031,760 , GRCh37.p13 chr19: 20,140,260-20,142,569 ZNF682, LOC105372308
    nsv5014682copy number variation1nstd200human GRCh38 chr19: 19,980,151-20,053,961 , GRCh37.p13 chr19: 20,090,960-20,164,770 ZNF682, LOC101928960, 3 more genes
    nsv5014680copy number variation1nstd200human GRCh38 chr19: 19,942,820-20,419,584 , GRCh37.p13 chr19|NW_003571053.2: 1-336,837 , GRCh37.p13 chr19: 20,193,556-20,602,390 , LOC102724427, 27 more genes
    nsv5014679copy number variation1nstd200human GRCh38 chr19: 19,914,520-20,109,774 , GRCh37.p13 chr19: 20,025,329-20,193,556 BNIP3P12, LOC105372309, 9 more genes
    nsv4860703copy number variation1nstd200human GRCh37 chr19: 20,142,376-20,143,112 , GRCh38.p12 chr19: 20,031,567-20,032,303 LOC105372308, LOC101928960, 1 more genes
    nsv4729750copy number variation1nstd102humanPathogenic GRCh37 chr19: 14,286,624-20,956,753 , GRCh38.p12 chr19: 14,175,812-20,773,947 LOC105372309, RAB8A, 269 more genes
    nsv4680854copy number variation1nstd189human GRCh37.p13 chr19: 20,124,696-20,611,032 , GRCh38.p12 chr19: 20,013,887-20,428,226 , ZNF90, 25 more genes
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