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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5684426mobile element insertion2nstd211human GRCh38 chr2: 105,401,082-105,401,082 , GRCh37.p13 chr2: 106,017,539-106,017,539 FHL2
    nsv5564336copy number variation1nstd102humanUncertain significance GRCh37 chr2: 105,977,730-106,002,983 , GRCh38.p12 chr2: 105,361,273-105,386,526 FHL2
    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
    nsv5434390copy number variation1nstd206human GRCh38 chr2: 105,402,550-105,402,604 , GRCh37.p13 chr2: 106,019,007-106,019,061 FHL2
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv5033955inversion1nstd200human GRCh38 chr2: 103,800,446-187,202,765 , GRCh37.p13 chr2: 104,416,904-188,067,492 , EDDM3CP, 1184 more genes
    nsv4893086copy number variation1nstd200human GRCh38 chr2: 105,435,989-105,437,121 , GRCh37.p13 chr2: 106,052,446-106,053,578 FHL2
    nsv4879764inversion1nstd200human GRCh37 chr2: 104,416,904-188,067,492 , GRCh38.p12 chr2: 103,800,446-187,202,765 , ACMSD, 1184 more genes
    nsv4786734copy number variation1nstd200human GRCh37 chr2: 106,052,446-106,053,578 , GRCh38.p12 chr2: 105,435,989-105,437,121 FHL2
    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
    nsv4518733copy number variation1nstd166human GRCh37.p13 chr2: 106,035,579-106,042,498 , GRCh38.p12 chr2: 105,419,122-105,426,041 FHL2
    nsv4463317mobile element insertion1nstd166human GRCh37.p13 chr2: 106,032,114-106,032,114 , GRCh38.p12 chr2: 105,415,657-105,415,657 FHL2
    nsv4462601mobile element insertion1nstd166human GRCh37.p13 chr2: 106,029,020-106,029,020 , GRCh38.p12 chr2: 105,412,563-105,412,563 FHL2
    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
    nsv4451036copy number variation1nstd102humanUncertain significance GRCh37 chr2: 104,816,400-106,617,614 , GRCh38.p12 chr2: 104,199,942-106,001,158 LINC02946, LOC105373529, 31 more genes
    nsv4343306sequence alteration1nstd166human GRCh37.p13 chr2: 106,020,462-106,029,833 , GRCh38.p12 chr2: 105,404,005-105,413,376 FHL2
    nsv4069943copy number variation1nstd166human GRCh37.p13 chr2: 106,034,813-106,036,881 , GRCh38.p12 chr2: 105,418,356-105,420,424 FHL2
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