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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5829883copy number variation1nstd209human GRCh38 chr1: 248,407,204-248,417,089 , GRCh37.p13 chr1: 248,570,505-248,580,390 OR2T1
    nsv5610483insertion3nstd207human GRCh38 chr1: 248,404,195-248,404,195 , GRCh37.p13 chr1: 248,567,496-248,567,496 OR2T1
    nsv5448739copy number variation1nstd206human GRCh38 chr1: 247,661,000-248,560,600 , GRCh37.p13 chr1: 247,824,302-248,723,901 OR14A2, OR2AJ1, 49 more genes
    nsv5446516copy number variation1nstd206human GRCh38 chr1: 248,402,364-248,449,364 , GRCh37.p13 chr1: 248,565,665-248,612,665 OR2T7, OR2T1
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5218648copy number variation1nstd204human GRCh38.p13 chr1: 248,405,158-248,415,050 , GRCh37.p13 chr1: 248,568,459-248,578,351 OR2T1
    nsv5217699copy number variation1nstd204human GRCh38.p13 chr1: 248,406,904-248,409,218 , GRCh37.p13 chr1: 248,570,205-248,572,519 OR2T1
    nsv5212448copy number variation1nstd204human GRCh38.p13 chr1: 248,406,004-248,410,409 , GRCh37.p13 chr1: 248,569,305-248,573,710 OR2T1
    nsv5203555copy number variation1nstd204human GRCh38.p13 chr1: 248,404,301-248,410,300 , GRCh37.p13 chr1: 248,567,602-248,573,601 OR2T1
    nsv5201336copy number variation1nstd204human GRCh38.p13 chr1: 248,407,404-248,411,909 , GRCh37.p13 chr1: 248,570,705-248,575,210 OR2T1
    nsv4904632copy number variation1nstd200human GRCh38 chr1: 248,339,421-248,712,442 , GRCh37.p13 chr1: 248,502,723-248,865,807 LOC105373277, OR14I1, 19 more genes
    nsv4904628copy number variation1nstd200human GRCh38 chr1: 247,906,731-248,623,796 , GRCh37.p13 chr1: 248,070,033-248,787,097 OR2T6, OR2M5, 38 more genes
    nsv4891882copy number variation1nstd200human GRCh38 chr1: 248,305,640-248,605,229 , GRCh37.p13 chr1: 248,468,942-248,768,530 OR2T29, OR2T2, 15 more genes
    nsv4785805copy number variation1nstd200human GRCh37 chr1: 248,468,942-248,768,530 , GRCh38.p12 chr1|NT_187646.1: 1-162,213 , GRCh38.p12 chr1: 248,305,640-248,605,229 , GRCh38.p12 chr1|NT_187518.1: 1-165,835 OR2AS2P, LOC105373277, 15 more genes
    nsv4728429copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 246,853,199-249,181,899 , GRCh38.p12 chr1: 246,689,897-248,887,700 ZNF124, TRIM58, 105 more genes
    nsv4684187copy number variation1nstd102humanPathogenic GRCh37 chr1: 210,152,794-249,218,992 , GRCh38.p12 chr1: 209,979,449-248,924,793 HLX-AS1, OPN3, 740 more genes
    nsv4679697copy number variation1nstd189human GRCh37.p13 chr1: 248,316,003-248,636,016 , GRCh38.p12 chr1: 248,152,701-248,472,715 OR2M4, OR2T1, 13 more genes
    nsv4679558copy number variation1nstd189human GRCh37.p13 chr1: 248,065,820-248,845,226 , GRCh38.p12 chr1: 247,902,518-248,681,925 OR2M4, OR2L2, 42 more genes
    nsv4674140copy number variation1nstd102humanPathogenic GRCh37 chr1: 204,045,948-249,218,992 , GRCh38.p12 chr1: 204,076,820-248,924,793 RNA5S8, NTPCR, 893 more genes
    nsv4581049copy number variation1nstd183human GRCh37 chr1: 248,509,495-248,649,577 , GRCh38.p12 chr1: 248,346,193-248,486,276 , GRCh38.p12 chr1|NT_187518.1: 1-140,316 , GRCh38.p12 chr1|NT_187646.1: 1-136,694 OR2T1, OR2T7, 7 more genes
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