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Items: 1 to 20 of 134

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5880667copy number variation1nstd209human GRCh38 chr2: 102,887,961-102,888,124 , GRCh37.p13 chr2: 103,504,420-103,504,583 LINC01796
    nsv5692632mobile element insertion1nstd211human GRCh38 chr2: 102,890,126-102,890,126 , GRCh37.p13 chr2: 103,506,585-103,506,585 LINC01796
    nsv5558142mobile element insertion1nstd206human GRCh38 chr2: 102,295,972-141,288,199 , GRCh37.p13 chr2: 102,912,432-142,045,768 , LOC105373587, 623 more genes
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5435706copy number variation1nstd206human GRCh38 chr2: 102,887,964-102,888,125 , GRCh37.p13 chr2: 103,504,423-103,504,584 LINC01796
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv4893003copy number variation1nstd200human GRCh38 chr2: 102,893,635-102,896,019 , GRCh37.p13 chr2: 103,510,094-103,512,477 LINC01796
    nsv4786679copy number variation1nstd200human GRCh37 chr2: 103,510,094-103,512,477 , GRCh38.p12 chr2: 102,893,635-102,896,019 LINC01796
    nsv4786678copy number variation1nstd200human GRCh37 chr2: 103,505,139-103,505,191 , GRCh38.p12 chr2: 102,888,680-102,888,732 LINC01796
    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
    nsv4656173copy number variation1nstd186human GRCh37 chr2: 103,504,423-103,504,584 , GRCh38.p12 chr2: 102,887,964-102,888,125 LINC01796
    nsv4533632insertion1nstd166human GRCh37.p13 chr2: 103,488,136-103,488,136 , GRCh38.p12 chr2: 102,871,677-102,871,677 LINC01796
    nsv4520105copy number variation1nstd166human GRCh37.p13 chr2: 103,504,423-103,504,584 , GRCh38.p12 chr2: 102,887,964-102,888,125 LINC01796
    nsv4463165mobile element insertion1nstd166human GRCh37.p13 chr2: 103,497,164-103,497,164 , GRCh38.p12 chr2: 102,880,705-102,880,705 LINC01796
    nsv4462898mobile element insertion1nstd166human GRCh37.p13 chr2: 103,504,374-103,504,374 , GRCh38.p12 chr2: 102,887,915-102,887,915 LINC01796
    nsv4454805copy number variation1nstd102humanUncertain significance GRCh37 chr2: 102,917,327-106,755,564 , GRCh38.p12 chr2: 102,300,867-106,139,108 LOC105373521, LOC107985927, 53 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
    nsv3907326copy number variation1nstd102humanPathogenic GRCh38 chr2: 97,672,522-110,211,318 , GRCh37 chr2: 98,288,985-110,968,895 , NCBI36 chr2: 97,655,417-110,326,184 RPL22P11, PANTR1, 212 more genes
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