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Items: 1 to 20 of 119

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5871480copy number variation1nstd209human GRCh38 chr19: 11,800,297-11,801,996 , GRCh37.p13 chr19: 11,911,112-11,912,811 ZNF491
    nsv5524833copy number variation1nstd206human GRCh38 chr19: 11,804,226-11,953,042 , GRCh37.p13 chr19: 11,915,041-12,063,857 ZNF69, LOC107985276, 8 more genes
    nsv5014528copy number variation1nstd200human GRCh38 chr19: 11,808,748-11,848,074 , GRCh37.p13 chr19: 11,919,563-11,958,889 ZNF439, VN2R13P, 2 more genes
    nsv5014527copy number variation1nstd200human GRCh38 chr19: 11,804,094-11,953,091 , GRCh37.p13 chr19: 11,914,909-12,063,906 VN2R14P, ZNF700, 8 more genes
    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
    nsv4631761copy number variation1nstd183human GRCh37 chr19: 11,915,185-12,061,384 , GRCh38.p12 chr19: 11,804,370-11,950,569 ZNF69, ZNF700, 7 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
    nsv4413974copy number variation1nstd174human GRCh37 chr19: 11,912,918-12,089,114 , GRCh38.p12 chr19: 11,802,103-11,978,299 ZNF700, ZNF491, 9 more genes
    nsv4370229copy number variation1nstd173human GRCh37 chr19: 11,912,917-12,069,592 , GRCh38.p12 chr19: 11,802,102-11,958,777 VN2R13P, LOC107985276, 8 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
    nsv4269574copy number variation1nstd166human GRCh37.p13 chr19: 11,914,923-12,063,857 , GRCh38.p12 chr19: 11,804,108-11,953,042 ZNF69, ZNF439, 8 more genes
    nsv3962442copy number variation1nstd168human GRCh38 chr19: 11,754,510-11,820,693 , GRCh37.p13 chr19: 11,865,325-11,931,508 ZNF491, ZNF441, 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
    nsv3922999copy number variation1nstd102humanPathogenic NCBI36 chr19: 10,240,071-12,946,266 , GRCh37.p13 chr19: 10,379,071-13,085,266 , GRCh38.p12 chr19: 10,268,395-12,974,452 ZNF433, MIR6794, 155 more genes
    nsv3922964copy number variation1nstd102humanPathogenic GRCh38 chr19: 10,319,474-13,777,860 , NCBI36 chr19: 10,291,150-13,749,674 , GRCh37 chr19: 10,430,150-13,888,674 SWSAP1, LOC105372284, 164 more genes
    nsv3920616copy number variation1nstd102humanLikely pathogenic NCBI36 chr19: 8,802,823-13,303,041 , GRCh37 chr19: 8,941,823-13,442,041 , GRCh38 chr19: 8,831,147-13,331,227 ACP5, GET3, 236 more genes
    nsv3920509copy number variation1nstd102humanUncertain significance GRCh37 chr19: 11,918,573-11,979,369 , NCBI36 chr19: 11,779,573-11,840,369 , GRCh38 chr19: 11,807,758-11,868,554 ZNF491, ZNF439, 2 more genes
    nsv3919036copy number variation1nstd102humanPathogenic GRCh37 chr19: 11,628,640-13,336,101 , NCBI36 chr19: 11,489,640-13,197,101 , GRCh38 chr19: 11,517,825-13,225,287 ZNF763, RTBDN, 105 more genes
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