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Items: 1 to 20 of 259

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7075365inversion1nstd229human GRCh38 chr9: 94,549,389-100,549,990 , GRCh37.p13 chr9: 97,311,671-103,312,272 PCAT7, ANKS6, 128 more genes
    nsv7073280inversion1nstd229human GRCh38 chr9: 99,040,855-99,040,882 , GRCh37.p13 chr9: 101,803,137-101,803,164 COL15A1
    nsv6877998copy number variation1nstd229human GRCh38 chr9: 98,997,941-98,999,947 , GRCh37.p13 chr9: 101,760,223-101,762,229 COL15A1
    nsv6875815copy number variation1nstd229human GRCh38 chr9: 99,016,201-99,021,700 , GRCh37.p13 chr9: 101,778,483-101,783,982 COL15A1
    nsv6875499copy number variation1nstd229human GRCh38 chr9: 98,983,510-98,983,709 , GRCh37.p13 chr9: 101,745,792-101,745,991 COL15A1
    nsv6874795copy number variation1nstd229human GRCh38 chr9: 98,970,033-98,970,124 , GRCh37.p13 chr9: 101,732,315-101,732,406 COL15A1
    nsv6869326copy number variation1nstd229human GRCh38 chr9: 98,969,542-98,971,461 , GRCh37.p13 chr9: 101,731,824-101,733,743 COL15A1
    nsv6868921copy number variation1nstd229human GRCh38 chr9: 98,982,588-98,985,106 , GRCh37.p13 chr9: 101,744,870-101,747,388 COL15A1
    nsv6866246copy number variation1nstd229human GRCh38 chr9: 98,985,219-98,988,929 , GRCh37.p13 chr9: 101,747,501-101,751,211 COL15A1
    nsv6864277copy number variation1nstd229human GRCh38 chr9: 98,963,193-98,963,543 , GRCh37.p13 chr9: 101,725,475-101,725,825 COL15A1
    nsv6864163copy number variation1nstd229human GRCh38 chr9: 99,000,778-99,016,063 , GRCh37.p13 chr9: 101,763,060-101,778,345 COL15A1
    nsv6860361copy number variation1nstd229human GRCh38 chr9: 98,949,453-98,966,707 , GRCh37.p13 chr9: 101,711,735-101,728,989 COL15A1
    nsv6859585copy number variation1nstd229human GRCh38 chr9: 99,070,310-99,082,259 , GRCh37.p13 chr9: 101,832,592-101,844,541 COL15A1
    nsv6858919copy number variation1nstd229human GRCh38 chr9: 98,942,817-99,140,966 , GRCh37.p13 chr9: 101,705,099-101,903,248 COL15A1, TGFBR1
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6632930copy number variation1nstd224human GRCh37 chr9: 101,765,841-101,778,321 , GRCh38.p12 chr9: 99,003,559-99,016,039 COL15A1
    nsv6632929copy number variation1nstd224human GRCh37 chr9: 101,699,804-101,728,521 , GRCh38.p12 chr9: 98,937,522-98,966,239 COL15A1
    nsv6452330copy number variation1nstd223human GRCh38 chr9: 98,985,219-98,988,924 , GRCh37.p13 chr9: 101,747,501-101,751,206 COL15A1
    nsv6447755copy number variation1nstd223human GRCh38 chr9: 92,901,749-100,255,234 , GRCh37.p13 chr9: 95,664,031-103,017,516 EIF4BP3, VN1R51P, 162 more genes
    nsv6315405copy number variation1nstd102humanUncertain significance GRCh37 chr9: 19,356,861-119,513,311 , GRCh38.p12 chr9: 19,356,863-116,751,032 RNU6-156P, GDA, 1425 more genes
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