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Items: 1 to 20 of 229

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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
    nsv6997889copy number variation1nstd229human GRCh38 chr17: 41,084,551-41,105,749 , GRCh37.p13 chr17: 39,240,803-39,262,001 KRTAP4-16, KRTAP4-8, 2 more genes
    nsv6994744copy number variation1nstd229human GRCh38 chr17: 41,087,401-41,113,400 , GRCh37.p13 chr17: 39,243,653-39,269,652 KRTAP4-9, KRTAP4-16, 1 more genes
    nsv6994391copy number variation1nstd229human GRCh38 chr17: 41,088,901-41,109,100 , GRCh37.p13 chr17: 39,245,153-39,265,352 KRTAP4-9, KRTAP4-16, 1 more genes
    nsv6990693copy number variation1nstd229human GRCh38 chr17: 41,088,701-41,110,000 , GRCh37.p13 chr17: 39,244,953-39,266,252 KRTAP4-9, KRTAP4-16, 1 more genes
    nsv6988608copy number variation1nstd229human GRCh38 chr17: 41,097,691-41,102,075 , GRCh37.p13 chr17: 39,253,943-39,258,327 KRTAP4-16, KRTAP4-8
    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
    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
    nsv6984661copy number variation1nstd229human GRCh38 chr17: 41,087,201-41,109,300 , GRCh37.p13 chr17: 39,243,453-39,265,552 KRTAP4-8, KRTAP4-9, 1 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
    nsv6979515copy number variation1nstd229human GRCh38 chr17: 41,084,356-41,105,899 , GRCh37.p13 chr17: 39,240,608-39,262,151 KRTAP4-9, KRTAP4-7, 2 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
    nsv6978373copy number variation1nstd229human GRCh38 chr17: 41,088,782-41,108,778 , GRCh37.p13 chr17: 39,245,034-39,265,030 KRTAP4-9, KRTAP4-16, 1 more genes
    nsv6511791copy number variation1nstd223human GRCh38 chr17: 41,083,401-41,102,600 , GRCh37.p13 chr17: 39,239,653-39,258,852 KRTAP4-16, KRTAP4-8, 1 more genes
    nsv6511233copy number variation1nstd223human GRCh38 chr17: 41,092,801-41,113,700 , GRCh37.p13 chr17: 39,249,053-39,269,952 KRTAP4-16, KRTAP4-9, 1 more genes
    nsv6509936copy number variation1nstd223human GRCh38 chr17: 41,093,762-41,113,982 , GRCh37.p13 chr17: 39,250,014-39,270,234 KRTAP4-9, KRTAP4-8, 1 more genes
    nsv6506446copy number variation1nstd223human GRCh38 chr17: 41,087,441-41,107,479 , GRCh37.p13 chr17: 39,243,693-39,263,731 KRTAP4-16, KRTAP4-9, 1 more genes
    nsv6503497copy number variation1nstd223human GRCh38 chr17: 41,088,943-41,108,946 , GRCh37.p13 chr17: 39,245,195-39,265,198 KRTAP4-9, KRTAP4-8, 1 more genes
    nsv6499605copy number variation1nstd223human GRCh38 chr17: 41,093,195-41,113,521 , GRCh37.p13 chr17: 39,249,447-39,269,773 KRTAP4-8, KRTAP4-9, 1 more genes
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