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Items: 1 to 20 of 269

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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
    nsv7069156inversion1nstd229human GRCh38 chr8: 103,453,664-108,809,244 , GRCh37.p13 chr8: 104,465,892-109,821,473 ZFPM2-AS1, HMGB1P46, 48 more genes
    nsv6857486copy number variation1nstd229human GRCh38 chr8: 108,484,764-108,519,376 , GRCh37.p13 chr8: 109,496,993-109,531,605 EMC2
    nsv6856587copy number variation1nstd229human GRCh38 chr8: 108,469,684-108,469,889 , GRCh37.p13 chr8: 109,481,913-109,482,118 EMC2
    nsv6843923copy number variation1nstd229human GRCh38 chr8: 108,461,601-108,468,400 , GRCh37.p13 chr8: 109,473,830-109,480,629 EMC2
    nsv6839215copy number variation1nstd229human GRCh38 chr8: 108,480,721-108,489,602 , GRCh37.p13 chr8: 109,492,950-109,501,831 EMC2
    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
    nsv6558789inversion1nstd223human GRCh38 chr8: 108,449,373-108,450,932 , GRCh37.p13 chr8: 109,461,602-109,463,161 EMC2
    nsv6433357copy number variation1nstd223human GRCh38 chr8: 108,462,601-108,463,797 , GRCh37.p13 chr8: 109,474,830-109,476,026 EMC2
    nsv6426727copy number variation1nstd223human GRCh38 chr8: 108,473,818-108,474,224 , GRCh37.p13 chr8: 109,486,047-109,486,453 EMC2
    nsv6419805copy number variation1nstd223human GRCh38 chr8: 108,451,308-108,451,674 , GRCh37.p13 chr8: 109,463,537-109,463,903 EMC2
    nsv6417776copy number variation1nstd223human GRCh38 chr8: 108,475,201-108,477,200 , GRCh37.p13 chr8: 109,487,430-109,489,429 EMC2
    nsv6315406copy number variation1nstd102humanPathogenic GRCh37 chr8: 84,712,253-146,295,771 , GRCh38.p12 chr8: 83,800,018-145,070,385 RHPN1, RPL18P7, 833 more genes
    nsv6314744copy number variation1nstd102humanPathogenic GRCh37 chr8: 96,496,503-146,295,711 , GRCh38.p12 chr8: 95,484,275-145,070,325 OSR2, LOC392268, 676 more genes
    nsv6313759copy number variation1nstd102humanPathogenic GRCh37 chr8: 70,382,990-146,295,771 , GRCh38.p12 chr8: 69,470,755-145,070,385 LOC101927066, NCAPGP1, 1014 more genes
    nsv6304511copy number variation1nstd186human GRCh37 chr8: 109,463,537-109,463,903 , GRCh38.p12 chr8: 108,451,308-108,451,674 EMC2
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