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Items: 1 to 20 of 386

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076156inversion1nstd229human GRCh38 chr8: 108,166,659-108,505,196 , GRCh37.p13 chr8: 109,178,888-109,517,425 EIF3E, LOC105375704, 2 more genes
    nsv7075711inversion1nstd229human GRCh38 chr8: 102,102,164-111,409,427 , GRCh37.p13 chr8: 103,114,392-112,421,656 LINC01181, LOC105375690, 118 more genes
    nsv7075327inversion1nstd229human GRCh38 chr8: 103,577,060-109,108,157 , GRCh37.p13 chr8: 104,589,288-110,120,386 OXR1, LOC101060000, 48 more genes
    nsv7069985inversion1nstd229human GRCh38 chr8: 106,070,234-108,375,396 , GRCh37.p13 chr8: 107,082,462-109,387,625 RNA5SP275, HMGB1P46, 15 more genes
    nsv7069156inversion1nstd229human GRCh38 chr8: 103,453,664-108,809,244 , GRCh37.p13 chr8: 104,465,892-109,821,473 ZFPM2-AS1, HMGB1P46, 48 more genes
    nsv7067128inversion1nstd229human GRCh38 chr8: 108,205,787-108,208,223 , GRCh37.p13 chr8: 109,218,016-109,220,452 EIF3E
    nsv7058096inversion1nstd229human GRCh38 chr8: 108,195,621-108,203,796 , GRCh37.p13 chr8: 109,207,850-109,216,025 EIF3E
    nsv6856228copy number variation1nstd229human GRCh38 chr8: 108,237,199-108,237,602 , GRCh37.p13 chr8: 109,249,428-109,249,831 EIF3E
    nsv6848418copy number variation1nstd229human GRCh38 chr8: 108,203,212-108,203,235 , GRCh37.p13 chr8: 109,215,441-109,215,464 EIF3E
    nsv6844628copy number variation1nstd229human GRCh38 chr8: 108,223,722-108,225,929 , GRCh37.p13 chr8: 109,235,951-109,238,158 EIF3E
    nsv6838559copy number variation1nstd229human GRCh38 chr8: 108,225,626-108,225,761 , GRCh37.p13 chr8: 109,237,855-109,237,990 EIF3E
    nsv6636450copy number variation1nstd102humanPathogenic GRCh37 chr8: 79,409,349-119,040,631 , GRCh38.p12 chr8: 78,497,114-118,028,392 MIR2053, RPS2P33, 507 more genes
    nsv6634360copy number variation1nstd102humanPathogenic GRCh37 chr8: 68,912,432-146,295,771 , GRCh38.p12 chr8: 68,000,197-145,070,385 WASHC5, LOC100132280, 1028 more genes
    nsv6632297copy number variation1nstd224human GRCh37 chr8: 109,020,400-109,787,856 , GRCh38.p12 chr8: 108,008,172-108,775,627 EIF3E, EMC2, 7 more genes
    nsv6565195inversion1nstd223human GRCh38 chr8: 108,226,271-108,227,163 , GRCh37.p13 chr8: 109,238,500-109,239,392 EIF3E
    nsv6562676inversion1nstd223human GRCh38 chr8: 108,236,999-108,237,290 , GRCh37.p13 chr8: 109,249,228-109,249,519 EIF3E
    nsv6430082copy number variation1nstd223human GRCh38 chr8: 108,223,722-108,225,927 , GRCh37.p13 chr8: 109,235,951-109,238,156 EIF3E
    nsv6426927copy number variation1nstd223human GRCh38 chr8: 108,201,801-108,202,800 , GRCh37.p13 chr8: 109,214,030-109,215,029 EIF3E
    nsv6422259copy number variation1nstd223human GRCh38 chr8: 108,207,301-108,209,600 , GRCh37.p13 chr8: 109,219,530-109,221,829 EIF3E
    nsv6421029copy number variation1nstd223human GRCh38 chr8: 108,223,701-108,224,800 , GRCh37.p13 chr8: 109,235,930-109,237,029 EIF3E
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