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Items: 1 to 20 of 973

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148254copy number variation1nstd102humanPathogenic GRCh38 chr17: 165,730-11,404,096 , GRCh37.p13 chr17: 396,627-11,307,413 RFLNB, C17orf100, 401 more genes
    nsv7145975copy number variation1nstd232human GRCh37.p13 chr17: 482,361-482,424 , GRCh38.p12 chr17: 579,121-579,184 , GRCh38.p12 chr17|NW_017363817.1: 138,598-138,661 VPS53
    nsv7144854insertion1nstd232human GRCh37.p13 chr17: 522,197-522,197 , GRCh38.p12 chr17: 618,957-618,957 , GRCh38.p12 chr17|NW_017363817.1: 178,434-178,434 VPS53
    nsv7143127copy number variation1nstd232human GRCh37.p13 chr17: 438,620-438,693 , GRCh38.p12 chr17: 535,380-535,453 , GRCh38.p12 chr17|NW_017363817.1: 94,857-94,930 VPS53
    nsv7141141insertion1nstd232human GRCh37.p13 chr17: 482,349-482,349 , GRCh38.p12 chr17: 579,109-579,109 , GRCh38.p12 chr17|NW_017363817.1: 138,586-138,586 VPS53
    nsv7139052copy number variation1nstd232human GRCh37.p13 chr17: 412,656-412,722 , GRCh38.p12 chr17: 509,416-509,482 , GRCh38.p12 chr17|NW_017363817.1: 68,893-68,959 VPS53
    nsv7137132copy number variation1nstd102humanUncertain significance GRCh37 chr17: 65,445-695,309 , GRCh38.p12 chr17: 215,654-792,069 RPS4XP17, RFLNB, 11 more genes
    nsv7098885copy number variation1nstd102humanUncertain significance GRCh37 chr17: 1-450,099 , GRCh38.p12 chr17|NW_003315952.3: 90,208-375,691 , GRCh38.p12 chr17: 150,208-546,859 LINC02091, VPS53, 8 more genes
    nsv7098743copy number variation1nstd102humanUncertain significance GRCh37 chr17: 422,368-2,585,096 , GRCh38.p12 chr17: 519,128-2,681,802 PAFAH1B1, RN7SL33P, 65 more genes
    nsv7098729copy number variation1nstd102humanPathogenic GRCh37 chr17: 422,368-1,945,151 , GRCh38.p12 chr17: 519,128-2,041,857 MYO1C, SERPINF1, 42 more genes
    nsv7094905copy number variation1nstd102humanUncertain significance GRCh37 chr17: 505,015-722,805 , GRCh38.p12 chr17: 601,775-819,565 , GRCh38.p12 chr17|NW_017363817.1: 161,252-281,919 GLOD4, TLCD3A, 6 more genes
    nsv7094896copy number variation1nstd102humanUncertain significance GRCh37 chr17: 422,368-1,680,740 , GRCh38.p12 chr17: 519,128-1,777,446 SLC43A2, LOC105371480, 34 more genes
    nsv7077982inversion1nstd229human GRCh38 chr17: 662,447-915,193 , GRCh37.p13 chr17: 565,687-818,433 GLOD4, LOC101927727, 6 more genes
    nsv7077886inversion1nstd229human GRCh38 chr17: 644,045-644,082 , GRCh37.p13 chr17: 547,285-547,322 VPS53
    nsv7077625inversion1nstd229human GRCh38 chr17: 626,377-3,112,687 , GRCh37.p13 chr17: 529,617-3,015,981 MIR3183, YWHAE, 75 more genes
    nsv7077460inversion1nstd229human GRCh38 chr17: 659,158-885,293 , GRCh37.p13 chr17: 562,398-788,533 TLCD3A, DBIL5P, 5 more genes
    nsv7070813inversion1nstd229human GRCh38 chr17: 181,363-638,312 , GRCh37.p13 chr17|NW_003315952.2: 31,154-270,261 , GRCh37.p13 chr17: 67,876-296,626 RFLNB, LOC105371425, 7 more genes
    nsv7070618inversion1nstd229human GRCh38 chr17: 426,050-796,506 , GRCh37.p13 chr17: 396,627-699,746 GEMIN4, MRM3, 6 more genes
    nsv7061183inversion1nstd229human GRCh38 chr17: 587,014-591,763 , GRCh37.p13 chr17: 490,254-495,003 VPS53
    nsv7060051inversion1nstd229human GRCh38 chr17: 689,006-865,724 , GRCh37.p13 chr17: 592,246-768,964 MRM3, VPS53, 5 more genes
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