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Items: 1 to 20 of 162

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5429360copy number variation1nstd206human GRCh38 chr1: 111,687,835-115,150,000 , GRCh37.p13 chr1: 112,230,457-115,692,621 , ST7L, 77 more genes
    nsv5381058copy number variation1nstd102humanPathogenic GRCh37 chr1: 102,021,465-119,737,478 , GRCh38.p12 chr1: 101,555,909-119,194,855 AMYP1, MIR4256, 320 more genes
    nsv5286762copy number variation1nstd204human GRCh37.p13 chr1: 113,412,224-113,526,937 , GRCh38.p13 chr1: 112,869,602-112,984,315 SLC16A1, AKR7A2P1, 6 more genes
    nsv5208846copy number variation1nstd204human GRCh37.p13 chr1: 113,414,923-113,526,922 , GRCh38.p13 chr1: 112,872,301-112,984,300 SLC16A1, AKR7A2P1, 6 more genes
    nsv4894420copy number variation1nstd200human GRCh38 chr1: 112,702,675-113,232,556 , GRCh37.p13 chr1: 113,245,297-113,775,178 RHOC, RPS19P2, 19 more genes
    nsv4894419copy number variation1nstd200human GRCh38 chr1: 112,670,692-113,135,319 , GRCh37.p13 chr1: 113,213,314-113,677,941 CAPZA1, SLC16A1-AS1, 17 more genes
    nsv4894418copy number variation1nstd200human GRCh38 chr1: 112,549,341-113,353,065 , GRCh37.p13 chr1: 113,091,963-113,895,687 LOC105378911, RNU7-70P, 23 more genes
    nsv4781130copy number variation1nstd200human GRCh37 chr1: 113,412,246-113,526,914 , GRCh38.p12 chr1: 112,869,624-112,984,292 , GRCh38.p12 chr1|NW_009646196.1: 1-74,871 SLC16A1, LOC107985189, 6 more genes
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4761183inversion1nstd199human GRCh37 chr1: 16,884,570-145,374,569 , GRCh38.p12 chr1: 16,558,075-149,528,945 , ABCA4, 2341 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4745469copy number variation1nstd199human GRCh37 chr1: 86,005,697-146,486,085 , GRCh38.p12 chr1: 85,540,014-149,528,945 , TAF13, 920 more genes
    nsv4579027copy number variation1nstd183human GRCh37 chr1: 113,375,437-113,852,815 , GRCh38.p12 chr1: 112,832,815-113,310,193 LINC01357, LOC105378911, 13 more genes
    nsv4451191copy number variation1nstd102humanUncertain significance GRCh37 chr1: 113,234,268-113,743,303 , GRCh38.p12 chr1: 112,691,646-113,200,681 MOV10, LRIG2, 19 more genes
    nsv4408250copy number variation1nstd174human GRCh37 chr1: 113,295,805-113,684,833 , GRCh38.p12 chr1: 112,753,183-113,142,211 SLC16A1, LRIG2, 10 more genes
    nsv4373134copy number variation1nstd173human GRCh37 chr1: 113,314,609-113,736,009 , GRCh38.p12 chr1: 112,771,987-113,193,387 RPS19P2, LINC01356, 11 more genes
    nsv4371088copy number variation1nstd173human GRCh37 chr1: 113,378,474-113,663,927 , GRCh38.p12 chr1: 112,835,852-113,121,305 LRIG2-DT, SLC16A1-AS1, 9 more genes
    nsv4370035copy number variation1nstd173human GRCh37 chr1: 113,308,186-113,733,041 , GRCh38.p12 chr1: 112,765,564-113,190,419 LOC105378911, RPS19P2, 11 more genes
    nsv4330538inversion1nstd166human GRCh37.p13 chr1: 94,223,082-113,632,613 , GRCh38.p12 chr1: 93,757,526-113,089,991 , AMPD2, 329 more genes
    nsv3900976copy number variation1nstd102humanUncertain significance NCBI36 chr1: 113,031,469-113,560,603 , GRCh38 chr1: 112,687,324-113,216,458 , GRCh37 chr1: 113,229,946-113,759,080 SLC16A1, AKR7A2P1, 19 more genes
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