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Items: 1 to 20 of 427

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7073436inversion1nstd229human GRCh38 chr12: 52,288,506-52,304,787 , GRCh37.p13 chr12: 52,682,290-52,698,571 KRT86, KRT81
    nsv7069901inversion1nstd229human GRCh38 chr12: 51,176,082-54,825,440 , GRCh37.p13 chr12: 51,569,865-55,219,224 , HOXC5, 158 more genes
    nsv7069507inversion1nstd229human GRCh38 chr12: 52,295,470-52,295,556 , GRCh37.p13 chr12: 52,689,254-52,689,340 KRT86
    nsv7068885inversion1nstd229human GRCh38 chr12: 52,296,024-52,301,816 , GRCh37.p13 chr12: 52,689,808-52,695,600 KRT86
    nsv7061604inversion1nstd229human GRCh38 chr12: 52,288,016-52,732,145 , GRCh37.p13 chr12: 52,681,800-53,125,929 KRT81, LOC400036, 22 more genes
    nsv7061367inversion1nstd229human GRCh38 chr12: 52,274,956-52,274,993 , GRCh37.p13 chr12: 52,668,740-52,668,777 KRT86
    nsv7058339inversion1nstd229human GRCh38 chr12: 52,297,181-52,304,492 , GRCh37.p13 chr12: 52,690,965-52,698,276 KRT86
    nsv6932874copy number variation1nstd229human GRCh38 chr12: 52,265,912-52,283,784 , GRCh37.p13 chr12: 52,659,696-52,677,568 KRT86, KRT88P
    nsv6931004copy number variation1nstd229human GRCh38 chr12: 52,238,701-52,423,200 , GRCh37.p13 chr12: 52,632,485-52,816,984 KRT84, KRT89P, 11 more genes
    nsv6923421copy number variation1nstd229human GRCh38 chr12: 52,272,201-52,278,100 , GRCh37.p13 chr12: 52,665,985-52,671,884 KRT86
    nsv6922911copy number variation1nstd229human GRCh38 chr12: 52,059,204-52,321,021 , GRCh37.p13 chr12: 52,452,988-52,714,805 KRT87P, KRT86, 14 more genes
    nsv6921500copy number variation1nstd229human GRCh38 chr12: 52,294,714-52,389,423 , GRCh37.p13 chr12: 52,688,498-52,783,207 KRT86, KRT83, 3 more genes
    nsv6921236copy number variation1nstd229human GRCh38 chr12: 52,293,566-52,300,507 , GRCh37.p13 chr12: 52,687,350-52,694,291 KRT86
    nsv6621859copy number variation1nstd224human GRCh37 chr12: 52,700,040-52,779,113 , GRCh38.p12 chr12: 52,306,256-52,385,329 KRT85, KRT84, 3 more genes
    nsv6621819copy number variation1nstd224human GRCh37 chr12: 52,702,656-52,779,360 , GRCh38.p12 chr12: 52,308,872-52,385,576 KRT85, KRT84, 3 more genes
    nsv6621818copy number variation3nstd224human GRCh37 chr12: 52,702,656-52,778,829 , GRCh38.p12 chr12: 52,308,872-52,385,045 KRT85, KRT86, 3 more genes
    nsv6621817copy number variation1nstd224human GRCh37 chr12: 52,700,040-52,779,159 , GRCh38.p12 chr12: 52,306,256-52,385,375 KRT85, KRT89P, 3 more genes
    nsv6621816copy number variation2nstd224human GRCh37 chr12: 52,700,040-52,778,829 , GRCh38.p12 chr12: 52,306,256-52,385,045 KRT85, KRT89P, 3 more genes
    nsv6621815copy number variation2nstd224human GRCh37 chr12: 52,695,630-52,779,391 , GRCh38.p12 chr12: 52,301,846-52,385,607 KRT89P, KRT83, 3 more genes
    nsv6621814copy number variation1nstd224human GRCh37 chr12: 52,695,630-52,779,351 , GRCh38.p12 chr12: 52,301,846-52,385,567 KRT86, KRT89P, 3 more genes
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