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Items: 1 to 20 of 124

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5207357copy number variation1nstd204human GRCh38.p13 chr2: 95,136,218-95,166,834 , GRCh37.p13 chr2: 95,801,963-95,832,579 ZNF2, ZNF514
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv4908119copy number variation1nstd200human GRCh38 chr2: 95,172,759-95,173,779 , GRCh37.p13 chr2: 95,838,504-95,839,524 ZNF2
    nsv4777059copy number variation1nstd200human GRCh37 chr2: 95,838,504-95,839,524 , GRCh38.p12 chr2: 95,172,759-95,173,779 ZNF2
    nsv4766632inversion1nstd199human GRCh37 chr2: 87,997,505-112,010,501 , GRCh38.p12 chr1: 125,085,511-144,884,066 , GRCh38.p12 chr2: 87,697,986-111,252,924 , GRCh38.p12 chr9: 40,649,907-63,450,751 , GRCh38.p12 chr9: 40,649,751-63,450,622 , ADRA2B, 706 more genes
    nsv4752571inversion1nstd199human GRCh37 chr2: 87,550,795-112,295,517 , GRCh38.p12 chr1: 125,085,511-144,884,066 , GRCh38.p12 chr2: 87,323,672-111,537,940 , GRCh38.p12 chr9: 40,649,907-63,450,751 , GRCh38.p12 chr9: 40,649,751-63,450,622 , ADRA2B, 723 more genes
    nsv4743379copy number variation1nstd199human GRCh37 chr2: 88,481,090-124,440,189 , GRCh38.p12 chr9: 40,649,751-63,450,622 , GRCh38.p12 chr9: 40,649,907-63,450,751 , GRCh38.p12 chr1: 125,085,511-144,884,066 , GRCh38.p12 chr2: 88,181,571-123,682,613 , EIF2AK3, 861 more genes
    nsv4534887insertion1nstd166human GRCh37.p13 chr2: 95,834,435-95,834,435 , GRCh38.p12 chr2: 95,168,690-95,168,690 ZNF2
    nsv4453674copy number variation1nstd102humanUncertain significance GRCh37 chr2: 95,800,306-96,097,247 , GRCh38.p12 chr2: 95,134,561-95,431,499 ZNF2, FAHD2A, 7 more genes
    nsv4451325copy number variation1nstd102humanUncertain significance GRCh37 chr2: 95,476,818-96,193,825 , GRCh38.p12 chr2: 94,811,073-95,528,077 FAHD2A, LOC100287523, 25 more genes
    nsv4067560copy number variation1nstd166human GRCh37.p13 chr2: 95,800,000-96,096,000 , GRCh38.p12 chr2: 95,134,255-95,430,252 ZNF2, KCNIP3, 7 more genes
    nsv4065612copy number variation1nstd166human GRCh37.p13 chr2: 95,796,937-95,961,216 , GRCh38.p12 chr2: 95,131,192-95,295,468 ZNF2, KCNIP3, 5 more genes
    nsv3914355copy number variation1nstd102humanUncertain significance NCBI36 chr2: 94,984,126-96,350,105 , GRCh37.p13 chr2: 95,620,399-96,986,378 , GRCh38.p12 chr2: 94,954,654-96,320,640 LOC101926959, TRE-CTC13-1, 43 more genes
    nsv3910630copy number variation1nstd102humanPathogenic NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331 DAZAP2P1, RPL36AP16, 2991 more genes
    nsv3906654copy number variation1nstd102humanPathogenic GRCh38 chr2: 91,443,218-102,334,856 , NCBI36 chr2: 90,981,410-102,317,748 , GRCh37 chr2: 91,617,683-102,951,316 CHEK2P3, LMAN2L, 197 more genes
    nsv3904893copy number variation1nstd102humanUncertain significance GRCh37 chr2: 95,799,814-96,159,275 , GRCh38 chr2: 95,134,069-95,493,527 , NCBI36 chr2: 95,163,541-95,523,002 ZNF2, KCNIP3, 10 more genes
    nsv3902899copy number variation1nstd102humanPathogenic NCBI36 chr2: 94,707,984-111,076,455 , GRCh38 chr2: 94,678,532-110,602,409 , GRCh37 chr2: 95,344,257-111,359,986 MTCO3P45, RPS21P2, 325 more genes
    nsv3899291copy number variation1nstd102humanPathogenic GRCh37 chr2: 95,618,109-103,868,854 , GRCh38 chr2: 94,817,406-103,252,396 , NCBI36 chr2: 94,846,878-103,235,286 IGKV2OR2-10, RNU4-8P, 178 more genes
    nsv3899030copy number variation1nstd102humanUncertain significance GRCh38 chr2: 95,079,592-95,408,265 , NCBI36 chr2: 95,109,064-95,437,740 , GRCh37 chr2: 95,745,337-96,074,013 ZNF2, KCNIP3, 8 more genes
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