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Items: 1 to 20 of 158

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5935874copy number variation1nstd209human GRCh38 chr19: 36,129,530-36,153,993 , GRCh37.p13 chr19: 36,620,432-36,644,895 CAPNS1, COX7A1, 1 more genes
    nsv5935442copy number variation1nstd209human GRCh38 chr19: 36,140,368-36,144,022 , GRCh37.p13 chr19: 36,631,270-36,634,924 CAPNS1, LOC105372385
    nsv5874844copy number variation1nstd209human GRCh38 chr19: 36,140,329-36,144,073 , GRCh37.p13 chr19: 36,631,231-36,634,975 LOC105372385, CAPNS1
    nsv5532202copy number variation1nstd206human GRCh38 chr19: 36,141,058-36,141,121 , GRCh37.p13 chr19: 36,631,960-36,632,023 CAPNS1
    nsv5289021copy number variation1nstd204human GRCh38.p13 chr19: 36,002,801-36,145,200 , GRCh37.p13 chr19: 36,493,703-36,636,102 LOC101927572, THAP8, 10 more genes
    nsv5024583copy number variation1nstd200human GRCh38 chr19: 36,131,032-36,147,111 , GRCh37.p13 chr19: 36,621,934-36,638,013 LOC105372385, CAPNS1
    nsv5024570copy number variation1nstd200human GRCh38 chr19: 35,722,805-36,225,611 , GRCh37.p13 chr19: 36,213,707-36,716,513 LOC105372385, ALKBH6, 34 more genes
    nsv4865133copy number variation1nstd200human GRCh37 chr19: 36,213,707-36,716,513 , GRCh38.p12 chr19: 35,722,805-36,225,611 KMT2B, PSENEN, 34 more genes
    nsv4680891copy number variation1nstd189human GRCh37.p13 chr19: 36,586,154-37,723,606 , GRCh38.p12 chr19: 36,095,252-37,232,704 CAPNS1, TBCB, 36 more genes
    nsv4457836copy number variation1nstd102humanUncertain significance GRCh37 chr19: 36,570,287-36,655,341 , GRCh38.p12 chr19: 36,079,385-36,164,439 OVOL3, TBCB, 5 more genes
    nsv4457372copy number variation1nstd102humanPathogenic GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575 ZNF461, LOC101927572, 735 more genes
    nsv4349605copy number variation1nstd102humanPathogenic GRCh37 chr19: 35,111,811-37,744,992 , GRCh38.p12 chr19: 34,620,906-37,254,090 ATP4A, RNY5P10, 129 more genes
    nsv4261063copy number variation1nstd166human GRCh37.p13 chr19: 36,638,705-36,638,759 , GRCh38.p12 chr19: 36,147,803-36,147,857 CAPNS1
    nsv4253388copy number variation1nstd166human GRCh37.p13 chr19: 36,630,410-36,630,618 , GRCh38.p12 chr19: 36,139,508-36,139,716 CAPNS1, LOC105372385
    nsv3961084inversion1nstd168human GRCh38 chr19: 36,102,738-37,299,603 , GRCh37.p13 chr19: 36,593,640-37,790,505 CAPNS1, TBCB, 38 more genes
    nsv3919296copy number variation1nstd102humanPathogenic NCBI36 chr19: 34,844,605-43,297,203 , GRCh37 chr19: 30,152,765-38,605,363 , GRCh38 chr19: 29,661,858-38,114,723 UBA2, ZNF529, 241 more genes
    nsv3916007copy number variation1nstd102humanPathogenic GRCh37 chr19: 30,162,231-38,393,630 , NCBI36 chr19: 34,854,071-43,085,470 , GRCh38 chr19: 29,671,324-37,902,990 MAG, RNU6-967P, 238 more genes
    nsv3913730copy number variation1nstd102humanPathogenic NCBI36 chr19: 11,199,618-49,821,491 , GRCh37 chr19: 11,338,618-45,129,651 , GRCh38 chr19: 11,227,942-44,626,354 BCKDHA, ADGRE5, 1102 more genes
    nsv3909857copy number variation1nstd102humanUncertain significance GRCh37 chr19: 36,475,577-38,399,402 , GRCh38.p12 chr19: 35,984,675-37,908,762 ZNF790, ZNF571-AS1, 72 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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