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Items: 1 to 20 of 264

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098813copy number variation1nstd102humanPathogenic GRCh37 chr12: 176,047-34,179,852 , GRCh38.p12 chr12: 66,881-34,026,917 TDGP1, RPS4XP14, 680 more genes
    nsv7072221inversion1nstd229human GRCh38 chr12: 4,055,290-11,695,188 , GRCh37.p13 chr12: 4,164,456-11,848,122 RN7SL69P, KLRA1P, 285 more genes
    nsv7068010inversion1nstd229human GRCh38 chr12: 7,025,778-10,225,656 , GRCh37.p13 chr12: 7,178,850-10,378,255 GOT2P3, CLEC2B, 123 more genes
    nsv7064008inversion1nstd229human GRCh38 chr12: 6,716,253-10,225,825 , GRCh37.p13 chr12: 6,825,419-10,378,424 PTMAP4, COPS7A, 153 more genes
    nsv6935594copy number variation1nstd229human GRCh38 chr12: 9,932,412-9,932,603 , GRCh37.p13 chr12: 10,085,011-10,085,202 CLEC2A
    nsv6935054copy number variation1nstd229human GRCh38 chr12: 9,902,670-9,903,571 , GRCh37.p13 chr12: 10,055,269-10,056,170 CLEC2A
    nsv6931402copy number variation1nstd229human GRCh38 chr12: 9,878,433-9,882,992 , GRCh37.p13 chr12: 10,031,032-10,035,591 CLEC2A, KLRF2
    nsv6931228copy number variation1nstd229human GRCh38 chr12: 9,876,670-9,947,880 , GRCh37.p13 chr12: 10,029,269-10,100,479 KLRF2, CLEC2A, 2 more genes
    nsv6929809copy number variation1nstd229human GRCh38 chr12: 9,887,974-9,892,307 , GRCh37.p13 chr12: 10,040,573-10,044,906 CLEC2A, KLRF2
    nsv6929272copy number variation1nstd229human GRCh38 chr12: 9,887,701-9,890,500 , GRCh37.p13 chr12: 10,040,300-10,043,099 KLRF2, CLEC2A
    nsv6928277copy number variation1nstd229human GRCh38 chr12: 9,923,391-9,924,300 , GRCh37.p13 chr12: 10,075,990-10,076,899 CLEC2A
    nsv6926616copy number variation1nstd229human GRCh38 chr12: 9,928,201-9,959,500 , GRCh37.p13 chr12: 10,080,800-10,112,099 CLEC2A, CLEC12A-AS1, 2 more genes
    nsv6925359copy number variation1nstd229human GRCh38 chr12: 9,844,941-9,894,082 , GRCh37.p13 chr12: 9,997,540-10,046,681 CLEC2A, CLEC2B, 2 more genes
    nsv6922166copy number variation1nstd229human GRCh38 chr12: 9,876,748-9,972,594 , GRCh37.p13 chr12: 10,029,347-10,125,193 CLEC12A, CLEC12A-AS1, 3 more genes
    nsv6920222copy number variation1nstd229human GRCh38 chr12: 9,908,601-9,911,900 , GRCh37.p13 chr12: 10,061,200-10,064,499 CLEC2A
    nsv6637726copy number variation1nstd102humanUncertain significance GRCh37 chr12: 10,049,346-10,322,120 , GRCh38.p12 chr12: 9,896,747-10,169,521 CLEC1B, LOC102724020, 14 more genes
    nsv6591935inversion1nstd223human GRCh38 chr12: 9,932,764-9,933,598 , GRCh37.p13 chr12: 10,085,363-10,086,197 CLEC2A
    nsv6474110copy number variation1nstd223human GRCh38 chr12: 9,876,746-9,972,593 , GRCh37.p13 chr12: 10,029,345-10,125,192 CLEC12A-AS1, CLEC2A, 3 more genes
    nsv6470428copy number variation1nstd223human GRCh38 chr12: 9,923,391-9,924,300 , GRCh37.p13 chr12: 10,075,990-10,076,899 CLEC2A
    nsv6470355copy number variation1nstd223human GRCh38 chr12: 9,903,053-9,904,944 , GRCh37.p13 chr12: 10,055,652-10,057,543 CLEC2A
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