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Items: 1 to 20 of 470

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7082315copy number variation1nstd229human GRCh38 chrX: 110,416,895-110,417,526 , GRCh37.p13 chrX: 109,660,123-109,660,754 AMMECR1, RTL9
    nsv7082314copy number variation1nstd229human GRCh38 chrX: 110,389,238-110,389,431 , GRCh37.p13 chrX: 109,632,466-109,632,659 AMMECR1, RTL9
    nsv7082313copy number variation1nstd229human GRCh38 chrX: 110,372,341-110,372,414 , GRCh37.p13 chrX: 109,615,569-109,615,642 AMMECR1, RTL9
    nsv7082312copy number variation1nstd229human GRCh38 chrX: 110,331,682-110,332,287 , GRCh37.p13 chrX: 109,574,910-109,575,515 LOC105373312, AMMECR1
    nsv7082311copy number variation1nstd229human GRCh38 chrX: 110,319,528-110,320,015 , GRCh37.p13 chrX: 109,562,756-109,563,243 AMMECR1, LOC105373312
    nsv7082310copy number variation1nstd229human GRCh38 chrX: 110,299,773-110,300,583 , GRCh37.p13 chrX: 109,543,001-109,543,811 AMMECR1
    nsv7082309copy number variation1nstd229human GRCh38 chrX: 110,291,366-110,685,524 , GRCh37.p13 chrX: 109,534,594-109,928,752 RTL9, GNG5B, 5 more genes
    nsv7082308copy number variation1nstd229human GRCh38 chrX: 110,278,293-110,278,913 , GRCh37.p13 chrX: 109,521,521-109,522,141 AMMECR1
    nsv7082307copy number variation1nstd229human GRCh38 chrX: 110,273,115-110,275,014 , GRCh37.p13 chrX: 109,516,343-109,518,242 AMMECR1
    nsv7082306copy number variation1nstd229human GRCh38 chrX: 110,231,901-110,237,500 , GRCh37.p13 chrX: 109,475,129-109,480,728 AMMECR1
    nsv7082305copy number variation1nstd229human GRCh38 chrX: 110,231,001-110,235,600 , GRCh37.p13 chrX: 109,474,229-109,478,828 AMMECR1
    nsv7082304copy number variation1nstd229human GRCh38 chrX: 110,231,001-110,235,500 , GRCh37.p13 chrX: 109,474,229-109,478,728 AMMECR1
    nsv7082303copy number variation1nstd229human GRCh38 chrX: 110,226,401-110,235,600 , GRCh37.p13 chrX: 109,469,629-109,478,828 AMMECR1
    nsv7082302copy number variation1nstd229human GRCh38 chrX: 110,218,911-110,223,316 , GRCh37.p13 chrX: 109,462,139-109,466,544 SNORD96B, AMMECR1
    nsv7082301copy number variation1nstd229human GRCh38 chrX: 110,217,152-110,223,315 , GRCh37.p13 chrX: 109,460,380-109,466,543 SNORD96B, AMMECR1
    nsv7082300copy number variation1nstd229human GRCh38 chrX: 110,213,661-110,213,746 , GRCh37.p13 chrX: 109,456,889-109,456,974 AMMECR1
    nsv7082295copy number variation1nstd229human GRCh38 chrX: 110,147,666-110,458,509 , GRCh37.p13 chrX: 109,390,894-109,701,737 LOC105373312, SNORD96B, 4 more genes
    nsv7055654inversion1nstd229human GRCh38 chrX: 110,384,816-110,389,704 , GRCh37.p13 chrX: 109,628,044-109,632,932 RTL9, AMMECR1
    nsv7052621inversion1nstd229human GRCh38 chrX: 103,826,879-110,334,422 , GRCh37.p13 chrX: 103,081,809-109,577,650 CSGALNACT2P2, LOC107985662, 82 more genes
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