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Items: 1 to 20 of 207

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076365inversion1nstd229human GRCh38 chr8: 114,461,125-114,899,538 , GRCh37.p13 chr8: 115,473,354-115,911,767 CARS1P2
    nsv7072142inversion1nstd229human GRCh38 chr8: 113,332,988-120,659,210 , GRCh37.p13 chr8: 114,345,217-121,671,450 ENPP2, RAD21-AS1, 67 more genes
    nsv7063957inversion1nstd229human GRCh38 chr8: 114,624,633-114,968,367 , GRCh37.p13 chr8: 115,636,862-115,980,596 LOC107986901, CARS1P2
    nsv7061580inversion1nstd229human GRCh38 chr8: 114,079,809-114,907,129 , GRCh37.p13 chr8: 115,092,038-115,919,358 LOC100420746, CARS1P2, 1 more genes
    nsv7061148inversion1nstd229human GRCh38 chr8: 114,778,273-115,346,707 , GRCh37.p13 chr8: 115,790,502-116,358,936 CARS1P2, LOC107986901
    nsv6848157copy number variation1nstd229human GRCh38 chr8: 114,720,098-115,034,123 , GRCh37.p13 chr8: 115,732,327-116,046,352 CARS1P2, LOC107986901
    nsv6839660copy number variation1nstd229human GRCh38 chr8: 114,734,195-114,899,413 , GRCh37.p13 chr8: 115,746,424-115,911,642 CARS1P2
    nsv6838837copy number variation1nstd229human GRCh38 chr8: 114,721,432-114,876,780 , GRCh37.p13 chr8: 115,733,661-115,889,009 CARS1P2
    nsv6637305copy number variation1nstd102humanUncertain significance GRCh37 chr8: 113,499,263-116,350,969 , GRCh38.p12 chr8: 112,487,034-115,338,740 RPL30P16, LOC100420746, 8 more genes
    nsv6637224copy number variation1nstd102humanPathogenic GRCh37 chr8: 112,234,557-133,668,379 , GRCh38.p12 chr8: 111,222,328-132,656,133 RNU4-37P, LOC100420215, 220 more genes
    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
    nsv6632730copy number variation1nstd224human GRCh37 chr8: 115,758,712-115,909,561 , GRCh38.p12 chr8: 114,746,483-114,897,332 CARS1P2
    nsv6427744copy number variation1nstd223human GRCh38 chr8: 114,285,921-115,216,172 , GRCh37.p13 chr8: 115,298,150-116,228,401 LOC107986901, CARS1P2, 2 more genes
    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
    nsv6315335copy number variation1nstd102humanPathogenic GRCh37 chr8: 115,662,767-117,718,250 , GRCh38.p12 chr8: 114,650,538-116,706,011 LOC107986968, EIF3H, 11 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
    nsv6136605copy number variation1nstd213human GRCh37 chr8: 86,730,000-120,700,001 , GRCh38.p12 chr8: 85,717,771-119,687,761 CALB1, CDH17, 421 more genes
    nsv6136300copy number variation1nstd213human GRCh37 chr8: 107,740,000-120,740,001 , GRCh38.p12 chr8: 106,727,772-119,727,761 EXT1, CCN3, 107 more genes
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