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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
    nsv5975905inversion1nstd209human GRCh38 chr19: 11,675,731-11,685,503 , GRCh37.p13 chr19: 11,786,546-11,796,318 ZNF833P
    nsv5971672insertion1nstd209human GRCh38 chr19: 11,672,602-11,672,602 , GRCh37.p13 chr19: 11,783,417-11,783,417 ZNF833P
    nsv5880733copy number variation1nstd209human GRCh38 chr19: 11,675,712-11,680,165 , GRCh37.p13 chr19: 11,786,527-11,790,980 ZNF833P
    nsv5555647sequence alteration1nstd206human GRCh38 chr19: 11,675,730-11,685,504 , GRCh37.p13 chr19: 11,786,545-11,796,319 ZNF833P
    nsv5530151copy number variation1nstd206human GRCh38 chr19: 11,672,602-11,672,698 , GRCh37.p13 chr19: 11,783,417-11,783,513 ZNF833P
    nsv5516037copy number variation1nstd206human GRCh38 chr19: 11,683,219-11,684,882 , GRCh37.p13 chr19: 11,794,034-11,795,697 ZNF833P
    nsv5287330copy number variation1nstd204human GRCh38.p13 chr19: 10,335,601-11,755,400 , GRCh37.p13 chr19: 10,446,277-11,866,215 AP1M2, C19orf38, 64 more genes
    nsv5286421copy number variation1nstd204human GRCh38.p13 chr19: 11,668,601-11,673,600 , GRCh37.p13 chr19: 11,779,416-11,784,415 ZNF833P
    nsv5011712copy number variation1nstd200human GRCh38 chr19: 11,677,005-11,677,113 , GRCh37.p13 chr19: 11,787,820-11,787,928 ZNF833P
    nsv4685775copy number variation1nstd102humannot provided GRCh37 chr19: 10,642,984-12,810,067 , GRCh38.p12 chr19: 10,532,308-12,699,253 SLC44A2, ZNF833P, 114 more genes
    nsv4676222copy number variation1nstd102humanUncertain significance GRCh37 chr19: 11,445,773-12,160,664 , GRCh38.p12 chr19: 11,335,097-12,049,849 ECSIT, MIR7974, 41 more genes
    nsv4451686copy number variation1nstd102humannot provided GRCh37 chr19: 10,642,984-12,810,067 , GRCh38.p12 chr19: 10,532,308-12,699,253 ODAD3, RNA5SP466, 114 more genes
    nsv4338402sequence alteration1nstd166human GRCh37.p13 chr19: 11,754,358-11,857,381 , GRCh38.p12 chr19: 11,643,543-11,746,566 ZNF823, ZNF833P, 2 more genes
    nsv4269749copy number variation1nstd166human GRCh37.p13 chr19: 11,690,922-11,942,753 , GRCh38.p12 chr19: 11,580,107-11,831,938 ZNF887P, VN2R12P, 8 more genes
    nsv4265462copy number variation1nstd166human GRCh37.p13 chr19: 11,787,703-11,787,780 , GRCh38.p12 chr19: 11,676,888-11,676,965 ZNF833P
    nsv4260787copy number variation1nstd166human GRCh37.p13 chr19: 11,787,860-11,788,190 , GRCh38.p12 chr19: 11,677,045-11,677,375 ZNF833P
    nsv4252564copy number variation1nstd166human GRCh37.p13 chr19: 11,785,521-11,786,204 , GRCh38.p12 chr19: 11,674,706-11,675,389 ZNF833P
    nsv3960276copy number variation1nstd168human GRCh38 chr19: 11,635,492-11,672,497 , GRCh37.p13 chr19: 11,746,307-11,783,312 HNRNPA1P10, ZNF887P, 1 more genes
    nsv3924466copy number variation1nstd102humanPathogenic NCBI36 chr19: 11,496,978-14,126,833 , GRCh38 chr19: 11,525,163-14,155,021 , GRCh37 chr19: 11,635,978-14,265,833 JUNB, ZNF442, 135 more genes
    nsv3923415copy number variation1nstd102humanPathogenic NCBI36 chr19: 10,286,934-14,020,806 , GRCh37 chr19: 10,425,934-14,159,806 , GRCh38 chr19: 10,315,258-14,048,994 MAN2B1, SWSAP1, 182 more genes
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