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Items: 1 to 20 of 205

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5453306copy number variation1nstd206human GRCh38 chr2: 102,335,213-102,356,302 , GRCh37.p13 chr2: 102,951,673-102,972,762 IL18R1, IL1RL1
    nsv5443515copy number variation1nstd206human GRCh38 chr2: 102,361,815-102,361,901 , GRCh37.p13 chr2: 102,978,275-102,978,361 IL18R1
    nsv5439658copy number variation1nstd206human GRCh38 chr2: 102,381,952-102,383,126 , GRCh37.p13 chr2: 102,998,412-102,999,586 IL18R1
    nsv5284921copy number variation1nstd204human GRCh38.p13 chr2: 102,381,922-102,383,155 , GRCh37.p13 chr2: 102,998,382-102,999,615 IL18R1
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv4892995copy number variation1nstd200human GRCh38 chr2: 102,381,952-102,383,126 , GRCh37.p13 chr2: 102,998,412-102,999,586 IL18R1
    nsv4786671copy number variation1nstd200human GRCh37 chr2: 102,998,412-102,999,586 , GRCh38.p12 chr2: 102,381,952-102,383,126 IL18R1
    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
    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
    nsv4454734copy number variation1nstd102humanUncertain significance GRCh37 chr2: 102,248,064-103,361,749 , GRCh38.p12 chr2: 101,631,602-102,745,290 TMEM182, SLC9A2, 14 more genes
    nsv4063332copy number variation1nstd166human GRCh37.p13 chr2: 102,998,412-102,999,586 , GRCh38.p12 chr2: 102,381,952-102,383,126 IL18R1
    nsv4063023copy number variation1nstd166human GRCh37.p13 chr2: 102,983,006-102,983,067 , GRCh38.p12 chr2: 102,366,546-102,366,607 IL18R1
    nsv4054645copy number variation1nstd166human GRCh37.p13 chr2: 102,973,678-102,973,770 , GRCh38.p12 chr2: 102,357,218-102,357,310 IL18R1
    nsv3971249copy number variation1nstd168human GRCh38 chr2: 102,371,787-102,425,578 , GRCh37.p13 chr2: 102,988,247-103,042,038 SDR42E1P5, IL18R1, 1 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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