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Items: 1 to 20 of 584

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148253copy number variation1nstd102humanPathogenic GRCh38 chr8: 449,893-23,854,904 , GRCh37.p13 chr8: 399,893-23,712,417 ENTPD4, LOC100421446, 447 more genes
    nsv7148110copy number variation1nstd102humanPathogenic GRCh37 chr8: 7,080,281-12,045,269 , GRCh38.p12 chr8: 7,222,759-12,187,760 DEFB106A, LOC101927997, 176 more genes
    nsv7074647inversion1nstd229human GRCh38 chr8: 11,585,028-14,417,119 , GRCh37.p13 chr8: 11,442,537-14,274,628 RNU7-153P, OR7E8P, 79 more genes
    nsv7069609inversion1nstd229human GRCh38 chr8: 7,102,414-12,683,056 , GRCh37.p13 chr8: 6,959,936-12,540,565 FAM90A20, LOC107986910, 201 more genes
    nsv7067997inversion1nstd229human GRCh38 chr8: 8,181,479-12,388,066 , GRCh37.p13 chr8: 8,039,001-12,245,575 TNKS, ZNF705D, 113 more genes
    nsv7065354inversion1nstd229human GRCh38 chr8: 9,129,798-15,405,439 , GRCh37.p13 chr8: 8,987,308-15,262,948 FAM167A, LOC729732, 132 more genes
    nsv7062538inversion1nstd229human GRCh38 chr8: 7,137,678-12,551,118 , GRCh37.p13 chr8: 6,995,200-12,408,627 MIR124-1, MFHAS1, 197 more genes
    nsv7059146inversion1nstd229human GRCh38 chr8: 7,352,588-12,547,775 , GRCh37.p13 chr8: 7,210,110-12,405,284 LOC107986910, HSPD1P2, 179 more genes
    nsv7058956inversion1nstd229human GRCh38 chr8: 8,224,000-12,734,745 , GRCh37.p13 chr8: 8,081,522-12,592,254 MIR3926-1, FAM90A25P, 129 more genes
    nsv6848527copy number variation1nstd229human GRCh38 chr8: 12,129,465-12,129,486 , GRCh37.p13 chr8: 11,986,974-11,986,995 FAM66D, LOC392196
    nsv6636968copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,049-18,936,715 , GRCh38.p12 chr8: 208,049-19,079,205 ZNF705B, NATP, 357 more genes
    nsv6636617copy number variation1nstd102humanPathogenic GRCh37 chr8: 8,093,066-12,548,732 , GRCh38.p12 chr8: 8,235,544-12,691,223 , GRCh38.p12 chr8|NW_018654717.1: 996,517-5,112,321 DEFB131D, RNU6-682P, 128 more genes
    nsv6634301complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,132,174 , GRCh37 chr8: 158,048-42,987,317 NAT1, NAT2, 758 more genes
    nsv6573530inversion1nstd223human GRCh38 chr8: 9,189,823-13,289,537 , GRCh37.p13 chr8: 9,047,333-13,147,046 MIR1322, LOC105379246, 115 more genes
    nsv6568725inversion1nstd223human GRCh38 chr8: 8,224,553-12,198,081 , GRCh37.p13 chr8: 8,082,075-12,055,590 USP17L2, DEFB136, 103 more genes
    nsv6558387inversion1nstd223human GRCh38 chr8: 8,224,415-12,440,176 , GRCh37.p13 chr8: 8,081,937-12,297,685 PRAG1, FAM85B, 118 more genes
    nsv6557112inversion1nstd223human GRCh38 chr8: 8,161,633-12,503,982 , GRCh37.p13 chr8: 8,019,155-12,361,491 BLK, DEFB109E, 120 more genes
    nsv6434716copy number variation1nstd223human GRCh38 chr8: 12,128,701-12,139,800 , GRCh37.p13 chr8: 11,986,210-11,997,309 USP17L2, USP17L7, 2 more genes
    nsv6434553copy number variation1nstd223human GRCh38 chr8: 12,126,801-12,135,300 , GRCh37.p13 chr8: 11,984,310-11,992,809 USP17L2, USP17L7, 2 more genes
    nsv6434237copy number variation1nstd223human GRCh38 chr8: 12,125,001-12,135,300 , GRCh37.p13 chr8: 11,982,510-11,992,809 USP17L7, USP17L2, 2 more genes
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