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Items: 1 to 20 of 189

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5919019copy number variation1nstd209human GRCh38 chr8: 26,939,516-27,553,947 , GRCh37.p13 chr8: 26,797,033-27,411,464 LOC105379339, TRIM35, 9 more genes
    nsv5489241copy number variation1nstd206human GRCh38 chr8: 27,275,976-27,445,064 , GRCh37.p13 chr8: 27,133,493-27,302,581 PTK2B, TRIM35, 1 more genes
    nsv5487287copy number variation1nstd206human GRCh38 chr8: 27,303,949-27,359,404 , GRCh37.p13 chr8: 27,161,466-27,216,921 PTK2B, TRIM35
    nsv5379181translocation1nstd200human GRCh38 chr8: 27,290,281-27,290,281 , GRCh38 chr8: 27,290,463-27,290,463 , GRCh37.p13 chr8: 27,147,980-27,147,980 , GRCh37.p13 chr8: 27,147,798-27,147,798 TRIM35
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv4959838copy number variation1nstd200human GRCh38 chr8: 27,297,988-27,299,045 , GRCh37.p13 chr8: 27,155,505-27,156,562 TRIM35
    nsv4768211inversion1nstd199human GRCh37 chr8: 23,474,464-53,327,098 , GRCh38.p12 chr8: 23,616,951-52,414,538 , ADRA1A, 411 more genes
    nsv4756879inversion1nstd199human GRCh37 chr8: 23,474,453-53,323,933 , GRCh38.p12 chr8: 23,616,940-52,411,373 , ADRA1A, 411 more genes
    nsv4748731copy number variation1nstd199human GRCh37 chr8: 27,148,048-27,153,063 , GRCh38.p12 chr8: 27,290,531-27,295,546 TRIM35
    nsv4728911copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 12,528,482-29,886,483 , GRCh38.p12 chr8: 12,670,973-30,028,967 NAT1, NAT2, 272 more genes
    nsv4675292copy number variation1nstd102humanPathogenic GRCh37 chr8: 24,305,969-28,673,405 , GRCh38.p12 chr8: 24,448,456-28,815,888 LOC112268023, GNRH1, 79 more genes
    nsv4601460copy number variation1nstd183human GRCh37 chr8: 27,166,945-27,249,002 , GRCh38.p12 chr8: 27,309,428-27,391,485 PTK2B, TRIM35
    nsv4456860copy number variation1nstd102humanUncertain significance GRCh37 chr8: 27,039,099-27,150,168 , GRCh38.p12 chr8: 27,181,582-27,292,651 TRIM35, STMN4, 1 more genes
    nsv4455606copy number variation1nstd102humanPathogenic GRCh37 chr8: 22,442,548-27,369,334 , GRCh38.p12 chr8: 22,585,035-27,511,817 PPP2R2A, LOC102723395, 91 more genes
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 LOC101929488, TEX15, 2105 more genes
    nsv4348018copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 12,546,855-35,816,855 , GRCh38.p12 chr8: 12,689,346-35,959,337 NAT1, NAT2, 343 more genes
    nsv3972390copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 12,556,004-34,374,150 , GRCh38.p12 chr8: 12,698,495-34,516,632 NAT1, NAT2, 335 more genes
    nsv3924532copy number variation1nstd102humanPathogenic NCBI36 chr8: 181,605-31,068,132 , GRCh38 chr8: 241,605-31,091,074 , GRCh37 chr8: 191,605-30,948,590 DEFB109B, GATA4, 585 more genes
    nsv3923600copy number variation1nstd102humanPathogenic NCBI36 chr8: 12,284,724-28,539,000 , GRCh37 chr8: 12,240,353-28,483,081 , GRCh38 chr8: 12,382,844-28,625,564 LOC105379340, LOC646708, 259 more genes
    nsv3923310copy number variation1nstd102humanPathogenic NCBI36 chr8: 166,452-146,264,902 , GRCh38 chr8: 226,452-145,068,712 , GRCh37 chr8: 176,452-146,294,098 LOC112268023, RPL23AP96, 2105 more genes
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