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Items: 1 to 20 of 217

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7073998inversion1nstd229human GRCh38 chr17: 32,918,710-41,148,753 , GRCh37.p13 chr17: 31,245,728-39,305,005 LOC105371750, C17orf78, 298 more genes
    nsv7066656inversion1nstd229human GRCh38 chr17: 40,822,205-41,582,529 , GRCh37.p13 chr17: 38,978,457-39,738,781 LOC105371777, KRT10, 69 more genes
    nsv6995491copy number variation1nstd229human GRCh38 chr17: 41,106,801-41,134,300 , GRCh37.p13 chr17: 39,263,053-39,290,552 KRTAP4-12, KRTAP4-11, 1 more genes
    nsv6994284copy number variation1nstd229human GRCh38 chr17: 41,099,128-41,119,644 , GRCh37.p13 chr17: 39,255,380-39,275,896 KRTAP4-9, KRTAP4-16, 1 more genes
    nsv6992297copy number variation1nstd229human GRCh38 chr17: 41,106,201-41,135,000 , GRCh37.p13 chr17: 39,262,453-39,291,252 KRTAP4-9, KRTAP4-11, 1 more genes
    nsv6990189copy number variation1nstd229human GRCh38 chr17: 41,117,584-41,121,203 , GRCh37.p13 chr17: 39,273,836-39,277,455 KRTAP4-11, KRTAP4-12
    nsv6988112copy number variation1nstd229human GRCh38 chr17: 41,098,201-41,119,400 , GRCh37.p13 chr17: 39,254,453-39,275,652 KRTAP4-11, KRTAP4-9, 2 more genes
    nsv6987013copy number variation1nstd229human GRCh38 chr17: 41,099,401-41,119,500 , GRCh37.p13 chr17: 39,255,653-39,275,752 KRTAP4-9, KRTAP4-16, 1 more genes
    nsv6986531copy number variation1nstd229human GRCh38 chr17: 41,109,624-41,132,885 , GRCh37.p13 chr17: 39,265,876-39,289,137 KRTAP4-11, KRTAP4-12
    nsv6986070copy number variation1nstd229human GRCh38 chr17: 41,110,401-41,135,000 , GRCh37.p13 chr17: 39,266,653-39,291,252 KRTAP4-11, KRTAP4-12
    nsv6984984copy number variation1nstd229human GRCh38 chr17: 38,377,708-42,855,253 , GRCh37.p13 chr17: 36,701,616-41,007,270 ZNF385C, AOC2, 248 more genes
    nsv6982861copy number variation1nstd229human GRCh38 chr17: 38,291,672-47,498,259 , GRCh37.p13 chr17: 36,510,266-45,575,625 KRT20, PLEKHH3, 442 more genes
    nsv6982025copy number variation1nstd229human GRCh38 chr17: 41,099,201-41,120,400 , GRCh37.p13 chr17: 39,255,453-39,276,652 KRTAP4-9, KRTAP4-16, 1 more genes
    nsv6978671copy number variation1nstd229human GRCh38 chr17: 41,097,901-41,119,400 , GRCh37.p13 chr17: 39,254,153-39,275,652 KRTAP4-11, KRTAP4-16, 2 more genes
    nsv6515430copy number variation1nstd223human GRCh38 chr17: 41,118,301-41,124,000 , GRCh37.p13 chr17: 39,274,553-39,280,252 KRTAP4-11, KRTAP4-12
    nsv6511909copy number variation1nstd223human GRCh38 chr17: 41,116,366-41,117,689 , GRCh37.p13 chr17: 39,272,618-39,273,941 KRTAP4-11
    nsv6510376copy number variation1nstd223human GRCh38 chr17: 41,117,932-41,140,199 , GRCh37.p13 chr17: 39,274,184-39,296,451 KRTAP4-11, KRTAP4-6, 1 more genes
    nsv6502790copy number variation1nstd223human GRCh38 chr17: 41,118,701-41,123,900 , GRCh37.p13 chr17: 39,274,953-39,280,152 KRTAP4-11, KRTAP4-12
    nsv6502051copy number variation1nstd223human GRCh38 chr17: 41,118,201-41,123,500 , GRCh37.p13 chr17: 39,274,453-39,279,752 KRTAP4-11, KRTAP4-12
    nsv6498916copy number variation1nstd223human GRCh38 chr17: 41,109,619-41,132,879 , GRCh37.p13 chr17: 39,265,871-39,289,131 KRTAP4-12, KRTAP4-11
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