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Items: 1 to 20 of 332

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093395copy number variation1nstd102humanPathogenic GRCh37 chr12: 64,609,458-70,352,103 , GRCh38.p12 chr12: 64,215,678-69,958,323 TODL, MIR6074, 116 more genes
    nsv7076679inversion1nstd229human GRCh38 chr12: 68,620,739-68,620,875 , GRCh37.p13 chr12: 69,014,519-69,014,655 RAP1B
    nsv7066132inversion1nstd229human GRCh38 chr12: 65,153,239-72,873,965 , GRCh37.p13 chr12: 65,547,019-73,267,745 IL26, RPL7P42, 119 more genes
    nsv7063686inversion1nstd229human GRCh38 chr12: 68,612,002-69,442,420 , GRCh37.p13 chr12: 69,005,782-69,836,200 RAP1B, YEATS4, 21 more genes
    nsv7060197inversion1nstd229human GRCh38 chr12: 64,990,820-72,253,420 , GRCh37.p13 chr12: 65,384,600-72,647,200 LINC02384, LOC105369809, 122 more genes
    nsv7059459inversion1nstd229human GRCh38 chr12: 68,623,271-69,442,390 , GRCh37.p13 chr12: 69,017,051-69,836,170 LOC100507250, RPS26P45, 21 more genes
    nsv6936644copy number variation1nstd229human GRCh38 chr12: 68,636,131-68,637,876 , GRCh37.p13 chr12: 69,029,911-69,031,656 RAP1B
    nsv6936123copy number variation1nstd229human GRCh38 chr12: 68,658,076-68,658,171 , GRCh37.p13 chr12: 69,051,856-69,051,951 RAP1B
    nsv6933832copy number variation1nstd229human GRCh38 chr12: 68,627,201-68,639,400 , GRCh37.p13 chr12: 69,020,981-69,033,180 SNORA70G, RPL10P12, 1 more genes
    nsv6933075copy number variation1nstd229human GRCh38 chr12: 68,494,505-68,795,230 , GRCh37.p13 chr12: 68,888,285-69,189,010 LOC100507250, SNORA70G, 9 more genes
    nsv6931737copy number variation1nstd229human GRCh38 chr12: 68,628,598-68,639,401 , GRCh37.p13 chr12: 69,022,378-69,033,181 RAP1B
    nsv6929804copy number variation1nstd229human GRCh38 chr12: 68,635,732-68,638,939 , GRCh37.p13 chr12: 69,029,512-69,032,719 RAP1B
    nsv6925003copy number variation1nstd229human GRCh38 chr12: 68,669,536-68,673,725 , GRCh37.p13 chr12: 69,063,316-69,067,505 RAP1B, LOC100507250
    nsv6924830copy number variation1nstd229human GRCh38 chr12: 68,670,493-68,672,846 , GRCh37.p13 chr12: 69,064,273-69,066,626 RAP1B, LOC100507250
    nsv6924031copy number variation1nstd229human GRCh38 chr12: 68,629,296-68,629,487 , GRCh37.p13 chr12: 69,023,076-69,023,267 RAP1B
    nsv6918768copy number variation1nstd229human GRCh38 chr12: 68,624,776-68,627,661 , GRCh37.p13 chr12: 69,018,556-69,021,441 RAP1B, RPL10P12, 1 more genes
    nsv6635527copy number variation1nstd227human GRCh38.p12 chr12: 68,460,445-68,686,836 , GRCh37 chr12: 68,854,225-69,080,616 RAP1B, NUP107, 8 more genes
    nsv6595209inversion1nstd223human GRCh38 chr12: 66,057,683-70,685,410 , GRCh37.p13 chr12: 66,451,463-71,079,190 PSMC6P2, SNORA70G, 86 more genes
    nsv6594036inversion1nstd223human GRCh38 chr12: 66,057,593-72,798,778 , GRCh37.p13 chr12: 66,451,373-73,192,558 PSMC6P2, SNORA70G, 103 more genes
    nsv6593453inversion1nstd223human GRCh38 chr12: 66,057,683-71,774,167 , GRCh37.p13 chr12: 66,451,463-72,167,947 LOC105369833, RN7SL804P, 96 more genes
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