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Items: 1 to 20 of 134

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6856105copy number variation1nstd229human GRCh38 chr8: 66,408,493-66,420,700 , GRCh37.p13 chr8: 67,320,728-67,332,935 LOC102724687, RRS1-DT
    nsv6855693copy number variation1nstd229human GRCh38 chr8: 66,415,291-66,476,233 , GRCh37.p13 chr8: 67,327,526-67,388,468 RRS1, ADHFE1, 2 more genes
    nsv6636205copy number variation1nstd102humanUncertain significance GRCh37 chr8: 67,261,729-68,676,568 , GRCh38.p12 chr8: 66,349,494-67,764,333 C8orf44-SGK3, SNHG6, 36 more genes
    nsv6300837copy number variation1nstd186human GRCh37 chr8: 67,340,152-67,340,855 , GRCh38.p12 chr8: 66,427,917-66,428,620 RRS1, RRS1-DT, 1 more genes
    nsv6290731copy number variation1nstd102humanPathogenic GRCh37 chr8: 66,045,954-69,807,260 , GRCh38.p12 chr8: 65,133,719-68,895,025 LINC00967, LOC107986950, 64 more genes
    nsv6136681copy number variation1nstd213human GRCh37 chr8: 46,860,000-86,550,001 , GRCh38.p12 chr8: 45,948,378-85,637,772 CEBPD, EYA1, 519 more genes
    nsv5485338copy number variation1nstd206human GRCh38 chr8: 66,427,917-66,428,620 , GRCh37.p13 chr8: 67,340,152-67,340,855 LOC102724687, RRS1-DT, 1 more genes
    nsv5317589copy number variation1nstd204human GRCh38.p13 chr8: 66,411,276-66,741,302 , GRCh37.p13 chr8: 67,323,511-67,653,537 C8orf44, RRS1-DT, 11 more genes
    nsv5258948copy number variation1nstd204human GRCh38.p13 chr8: 66,411,201-66,741,300 , GRCh37.p13 chr8: 67,323,436-67,653,535 MYBL1, SGK3, 11 more genes
    nsv5244624copy number variation1nstd204human GRCh38.p13 chr8: 66,411,289-66,448,607 , GRCh37.p13 chr8: 67,323,524-67,360,842 RRS1, RRS1-DT, 2 more genes
    nsv4965406copy number variation1nstd200human GRCh38 chr8: 66,411,286-66,741,296 , GRCh37.p13 chr8: 67,323,521-67,653,531 VCPIP1, RRS1-DT, 11 more genes
    nsv4960704copy number variation1nstd200human GRCh38 chr8: 66,427,917-66,428,620 , GRCh37.p13 chr8: 67,340,152-67,340,855 RRS1, LOC102724687, 1 more genes
    nsv4829064copy number variation1nstd200human GRCh37 chr8: 67,323,521-67,653,531 , GRCh38.p12 chr8: 66,411,286-66,741,296 VCPIP1, RRS1-DT, 11 more genes
    nsv4821782copy number variation1nstd200human GRCh37 chr8: 67,340,152-67,340,855 , GRCh38.p12 chr8: 66,427,917-66,428,620 RRS1-DT, RRS1, 1 more genes
    nsv4456811copy number variation1nstd102humanPathogenic GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385 TERF1, LOC107986945, 1511 more genes
    nsv4456190copy number variation1nstd102humanPathogenic GRCh37 chr8: 65,280,508-67,782,846 , GRCh38.p12 chr8: 64,367,951-66,870,611 BHLHE22-AS1, VCPIP1, 41 more genes
    nsv4387546copy number variation1nstd173human GRCh37 chr8: 65,023,339-68,301,135 , GRCh38.p12 chr8: 64,110,782-67,388,900 , LOC105375885, 56 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
    nsv4318272inversion1nstd166human GRCh37.p13 chr8: 51,271,211-76,167,888 , GRCh38.p12 chr8: 50,358,651-75,255,653 , ASPH, 341 more genes
    nsv3924415copy number variation1nstd102humanPathogenic GRCh37 chr8: 61,431,781-67,571,260 , GRCh38 chr8: 60,519,222-66,659,025 , NCBI36 chr8: 61,594,335-67,733,814 RN7SKP135, TRIM55, 77 more genes
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