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Items: 1 to 20 of 106

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5971403insertion1nstd209human GRCh38 chr19: 9,606,524-9,606,524 , GRCh37.p13 chr19: 9,717,200-9,717,200 ZNF561
    nsv5934443copy number variation1nstd209human GRCh38 chr19: 9,619,946-9,620,078 , GRCh37.p13 chr19: 9,730,622-9,730,754 ZNF561, ZNF561-AS1
    nsv5715473mobile element insertion2nstd211human GRCh38 chr19: 9,606,534-9,606,534 , GRCh37.p13 chr19: 9,717,210-9,717,210 ZNF561
    nsv5550413insertion1nstd206human GRCh38 chr19: 9,606,534-9,606,575 , GRCh37.p13 chr19: 9,717,210-9,717,251 ZNF561
    nsv5522413copy number variation1nstd206human GRCh38 chr19: 9,596,500-9,605,808 , GRCh37.p13 chr19: 9,707,176-9,716,484 ZNF561, LOC105376914
    nsv5190884mobile element insertion1nstd203human GRCh38 chr19: 9,606,524-9,606,534 , GRCh37.p13 chr19: 9,717,200-9,717,210 ZNF561
    nsv5188214mobile element insertion1nstd203human GRCh38 chr19: 9,606,528-9,606,528 , GRCh37.p13 chr19: 9,717,204-9,717,204 ZNF561
    nsv5177516mobile element insertion1nstd203human GRCh38 chr19: 9,615,301-9,615,309 , GRCh37.p13 chr19: 9,725,977-9,725,985 ZNF561
    nsv5011552copy number variation1nstd200human GRCh38 chr19: 9,615,453-9,624,816 , GRCh37.p13 chr19: 9,726,129-9,735,492 ZNF561, ZNF561-AS1
    nsv4852931copy number variation1nstd200human GRCh37 chr19: 9,707,176-9,716,484 , GRCh38.p12 chr19: 9,596,500-9,605,808 ZNF561, LOC105376914
    nsv4729799copy number variation1nstd102humanUncertain significance GRCh37 chr19: 8,518,395-10,053,298 , GRCh38.p12 chr19: 8,453,511-9,942,622 ZNF426-DT, ADAMTS10, 61 more genes
    nsv4630022copy number variation1nstd183human GRCh37 chr19: 9,696,925-9,763,152 , GRCh38.p12 chr19: 9,586,249-9,652,476 LOC105376914, ZNF561, 2 more genes
    nsv4624689copy number variation1nstd183human GRCh37 chr19: 9,663,138-9,806,979 , GRCh38.p12 chr19: 9,552,462-9,696,303 ZNF121, ZNF562, 5 more genes
    nsv4576643mobile element insertion1nstd166human GRCh37.p13 chr19: 9,717,200-9,717,200 , GRCh38.p12 chr19: 9,606,524-9,606,524 ZNF561
    nsv4436244complex substitution1nstd102humanUncertain significance GRCh38.p12 chr19: 8,891,157-9,974,378 , GRCh37 chr19: 9,001,833-10,085,054 PIN1, UBE2L4, 51 more genes
    nsv4266123copy number variation1nstd166human GRCh37.p13 chr19: 9,707,176-9,716,484 , GRCh38.p12 chr19: 9,596,500-9,605,808 ZNF561, LOC105376914
    nsv3968797copy number variation1nstd168human GRCh38 chr19: 9,573,277-9,617,703 , GRCh37.p13 chr19: 9,683,953-9,728,379 ZNF561, LOC105376914, 1 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
    nsv3914351copy number variation1nstd102humanPathogenic NCBI36 chr19: 1,923,244-9,620,555 , GRCh38 chr19: 1,972,245-9,648,879 , GRCh37 chr19: 1,972,244-9,759,555 SEMA6B, RANBP3-DT, 299 more genes
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 ZNF321P, ZNF861P, 2443 more genes
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