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Items: 1 to 20 of 149

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7069901inversion1nstd229human GRCh38 chr12: 51,176,082-54,825,440 , GRCh37.p13 chr12: 51,569,865-55,219,224 , HOXC5, 158 more genes
    nsv6937766copy number variation1nstd229human GRCh38 chr12: 52,169,803-52,173,630 , GRCh37.p13 chr12: 52,563,587-52,567,414 KRT80
    nsv6935923copy number variation1nstd229human GRCh38 chr12: 52,190,718-52,194,293 , GRCh37.p13 chr12: 52,584,502-52,588,077 KRT80
    nsv6935500copy number variation1nstd229human GRCh38 chr12: 52,180,882-52,181,039 , GRCh37.p13 chr12: 52,574,666-52,574,823 KRT80
    nsv6930803copy number variation1nstd229human GRCh38 chr12: 52,182,964-52,182,994 , GRCh37.p13 chr12: 52,576,748-52,576,778 KRT80
    nsv6929331copy number variation1nstd229human GRCh38 chr12: 52,141,005-52,179,068 , GRCh37.p13 chr12: 52,534,789-52,572,852 KRT80
    nsv6927829copy number variation1nstd229human GRCh38 chr12: 52,134,820-52,236,507 , GRCh37.p13 chr12: 52,528,604-52,630,291 KRT7, LINC02874, 3 more genes
    nsv6925637copy number variation1nstd229human GRCh38 chr12: 52,119,028-52,181,774 , GRCh37.p13 chr12: 52,512,812-52,575,558 KRT80
    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
    nsv6922670copy number variation1nstd229human GRCh38 chr12: 52,167,511-52,183,380 , GRCh37.p13 chr12: 52,561,295-52,577,164 KRT80
    nsv6621708copy number variation1nstd224human GRCh37 chr12: 52,515,244-52,574,923 , GRCh38.p12 chr12: 52,121,460-52,181,139 KRT80
    nsv6473819copy number variation1nstd223human GRCh38 chr12: 52,166,503-52,258,794 , GRCh37.p13 chr12: 52,560,287-52,652,578 KRT80, LINC02874, 5 more genes
    nsv6466687copy number variation1nstd223human GRCh38 chr12: 52,119,028-52,181,774 , GRCh37.p13 chr12: 52,512,812-52,575,558 KRT80
    nsv6462334copy number variation1nstd223human GRCh38 chr12: 52,167,511-52,183,380 , GRCh37.p13 chr12: 52,561,295-52,577,164 KRT80
    nsv6462229copy number variation1nstd223human GRCh38 chr12: 52,059,204-52,321,021 , GRCh37.p13 chr12: 52,452,988-52,714,805 LINC02874, SMIM41, 14 more genes
    nsv6460327copy number variation1nstd223human GRCh38 chr12: 52,186,234-52,186,939 , GRCh37.p13 chr12: 52,580,018-52,580,723 KRT80
    nsv6457965copy number variation1nstd223human GRCh38 chr12: 52,169,803-52,173,625 , GRCh37.p13 chr12: 52,563,587-52,567,409 KRT80
    nsv6143026copy number variation1nstd206human GRCh38 chr12: 48,500,915-111,724,058 , GRCh37.p13 chr12: 48,894,698-112,161,862 , LINC00592, 1206 more genes
    nsv6132252copy number variation1nstd213human GRCh37 chr12: 51,940,000-52,650,001 , GRCh38.p12 chr12: 51,546,216-52,256,217 ACVR1B, KRT80, 22 more genes
    nsv5857956copy number variation1nstd209human GRCh38 chr12: 52,165,284-52,169,063 , GRCh37.p13 chr12: 52,559,068-52,562,847 KRT80
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