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Items: 1 to 20 of 203

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099225copy number variation1nstd231human GRCh38.p12 chr1: 111,381,594-114,553,029 , GRCh37 chr1: 111,924,216-115,095,650 ADORA3, RHOC, 74 more genes
    nsv7095695copy number variation1nstd102humanPathogenic GRCh37 chr1: 111,145,905-114,454,813 , GRCh38.p12 chr1: 110,603,283-113,912,191 LOC107985189, RNU6-792P, 83 more genes
    nsv6640088copy number variation1nstd229human GRCh38 chr1: 111,721,750-111,721,843 , GRCh37.p13 chr1: 112,264,372-112,264,465 INKA2
    nsv6640056copy number variation1nstd229human GRCh38 chr1: 111,719,609-111,722,974 , GRCh37.p13 chr1: 112,262,231-112,265,596 INKA2
    nsv6549317inversion1nstd223human GRCh38 chr1: 111,078,274-116,976,218 , GRCh37.p13 chr1: 111,620,896-117,518,840 RNU6-792P, TXNP3, 141 more genes
    nsv6332804copy number variation1nstd223human GRCh38 chr1: 111,753,401-111,761,400 , GRCh37.p13 chr1: 112,296,023-112,304,022 DDX20, LOC101928718, 1 more genes
    nsv6315782copy number variation1nstd223human GRCh38 chr1: 111,753,044-111,754,444 , GRCh37.p13 chr1: 112,295,666-112,297,066 LOC101928718, INKA2, 1 more genes
    nsv6313675copy number variation1nstd102humanPathogenic GRCh37 chr1: 95,046,805-114,714,931 , GRCh38.p12 chr1: 94,581,249-114,172,309 LINC01307, FTLP17, 320 more genes
    nsv6313671copy number variation1nstd102humanPathogenic GRCh37 chr1: 111,647,582-121,343,783 , GRCh38.p12 chr1: 111,104,960-121,601,985 GAPDHP23, RNA5SP56, 243 more genes
    nsv6299084copy number variation1nstd186human GRCh37 chr1: 112,230,457-115,692,621 , GRCh38.p12 chr1: 111,687,835-115,150,000 , WNT2B, 77 more genes
    nsv6217715insertion1nstd214human GRCh38 chr1: 111,755,128-111,755,128 , GRCh37.p13 chr1: 112,297,750-112,297,750 DDX20, INKA2, 1 more genes
    nsv6133546copy number variation1nstd213human GRCh37 chr1: 111,330,000-112,310,001 , GRCh38.p12 chr1: 110,787,378-111,767,379 ADORA3, ATP5PB, 33 more genes
    nsv6133494copy number variation1nstd213human GRCh37 chr1: 112,060,000-112,550,001 , GRCh38.p12 chr1: 111,517,378-112,007,379 RAP1A, KCND3-IT1, 13 more genes
    nsv6051056insertion1nstd212human GRCh38 chr1: 111,755,128-111,755,128 , GRCh37.p13 chr1: 112,297,750-112,297,750 DDX20, INKA2, 1 more genes
    nsv5613983insertion1nstd207human GRCh38 chr1: 111,755,128-111,755,128 , GRCh37.p13 chr1: 112,297,750-112,297,750 DDX20, INKA2, 1 more genes
    nsv5429360copy number variation1nstd206human GRCh38 chr1: 111,687,835-115,150,000 , GRCh37.p13 chr1: 112,230,457-115,692,621 , ST7L, 77 more genes
    nsv5381058copy number variation1nstd102humanPathogenic GRCh37 chr1: 102,021,465-119,737,478 , GRCh38.p12 chr1: 101,555,909-119,194,855 AMYP1, MIR4256, 320 more genes
    nsv5288187copy number variation1nstd204human GRCh37.p13 chr1: 112,286,286-112,288,490 , GRCh38.p13 chr1: 111,743,664-111,745,868 INKA2, INKA2-AS1, 1 more genes
    nsv5211734copy number variation1nstd204human GRCh38.p13 chr1: 111,743,562-111,746,321 , GRCh37.p13 chr1: 112,286,184-112,288,943 INKA2-AS1, INKA2, 1 more genes
    nsv5202432copy number variation1nstd204human GRCh38.p13 chr1: 111,743,701-111,745,900 , GRCh37.p13 chr1: 112,286,323-112,288,522 INKA2, LOC101928718, 1 more genes
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