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Items: 1 to 20 of 335

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077154inversion1nstd229human GRCh38 chr12: 69,110,254-73,283,220 , GRCh37.p13 chr12: 69,504,034-73,677,000 MYRFL, CNOT2, 46 more genes
    nsv7066132inversion1nstd229human GRCh38 chr12: 65,153,239-72,873,965 , GRCh37.p13 chr12: 65,547,019-73,267,745 IL26, RPL7P42, 119 more genes
    nsv7063232inversion1nstd229human GRCh38 chr12: 70,397,724-70,397,744 , GRCh37.p13 chr12: 70,791,504-70,791,524 KCNMB4
    nsv7060760inversion1nstd229human GRCh38 chr12: 70,394,321-70,397,675 , GRCh37.p13 chr12: 70,788,101-70,791,455 KCNMB4
    nsv7060558inversion1nstd229human GRCh38 chr12: 70,418,350-70,418,481 , GRCh37.p13 chr12: 70,812,130-70,812,261 KCNMB4
    nsv7060197inversion1nstd229human GRCh38 chr12: 64,990,820-72,253,420 , GRCh37.p13 chr12: 65,384,600-72,647,200 LINC02384, LOC105369809, 122 more genes
    nsv7059006inversion1nstd229human GRCh38 chr12: 70,370,081-70,374,488 , GRCh37.p13 chr12: 70,763,861-70,768,268 KCNMB4
    nsv6934540copy number variation1nstd229human GRCh38 chr12: 70,408,431-70,408,623 , GRCh37.p13 chr12: 70,802,211-70,802,403 KCNMB4
    nsv6929844copy number variation1nstd229human GRCh38 chr12: 70,410,126-70,421,357 , GRCh37.p13 chr12: 70,803,906-70,815,137 KCNMB4
    nsv6927263copy number variation1nstd229human GRCh38 chr12: 70,368,949-70,369,325 , GRCh37.p13 chr12: 70,762,729-70,763,105 KCNMB4
    nsv6926707copy number variation1nstd229human GRCh38 chr12: 70,352,475-70,422,002 , GRCh37.p13 chr12: 70,746,255-70,815,782 CNOT2, KCNMB4
    nsv6925110copy number variation1nstd229human GRCh38 chr12: 70,365,534-70,366,242 , GRCh37.p13 chr12: 70,759,314-70,760,022 KCNMB4
    nsv6924091copy number variation1nstd229human GRCh38 chr12: 70,381,901-70,399,200 , GRCh37.p13 chr12: 70,775,681-70,792,980 KCNMB4
    nsv6923918copy number variation1nstd229human GRCh38 chr12: 70,386,364-70,442,216 , GRCh37.p13 chr12: 70,780,144-70,835,996 RNU4-65P, KCNMB4
    nsv6922684copy number variation1nstd229human GRCh38 chr12: 70,373,401-70,377,400 , GRCh37.p13 chr12: 70,767,181-70,771,180 KCNMB4
    nsv6921764copy number variation1nstd229human GRCh38 chr12: 70,388,215-70,393,064 , GRCh37.p13 chr12: 70,781,995-70,786,844 KCNMB4
    nsv6920223copy number variation1nstd229human GRCh38 chr12: 70,410,052-70,415,093 , GRCh37.p13 chr12: 70,803,832-70,808,873 KCNMB4
    nsv6919800copy number variation1nstd229human GRCh38 chr12: 70,393,201-70,394,707 , GRCh37.p13 chr12: 70,786,981-70,788,487 KCNMB4
    nsv6919412copy number variation1nstd229human GRCh38 chr12: 70,385,542-70,387,595 , GRCh37.p13 chr12: 70,779,322-70,781,375 KCNMB4
    nsv6595209inversion1nstd223human GRCh38 chr12: 66,057,683-70,685,410 , GRCh37.p13 chr12: 66,451,463-71,079,190 PSMC6P2, SNORA70G, 86 more genes
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