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Items: 1 to 20 of 243

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7066728inversion1nstd229human GRCh38 chr17: 42,678,051-42,699,940 , GRCh37.p13 chr17: 40,830,069-40,851,958 EZH1, CCR10, 1 more genes
    nsv6995669copy number variation1nstd229human GRCh38 chr17: 42,735,601-42,742,100 , GRCh37.p13 chr17: 40,887,619-40,894,118 EZH1
    nsv6990851copy number variation1nstd229human GRCh38 chr17: 42,664,969-42,743,375 , GRCh37.p13 chr17: 40,816,987-40,895,393 PLEKHH3, RPL34P30, 5 more genes
    nsv6987244copy number variation1nstd229human GRCh38 chr17: 42,729,494-42,733,663 , GRCh37.p13 chr17: 40,881,512-40,885,681 EZH1
    nsv6985364copy number variation1nstd229human GRCh38 chr17: 42,723,977-42,924,183 , GRCh37.p13 chr17: 40,875,995-41,076,200 AOC2, WNK4, 15 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
    nsv6983650copy number variation1nstd229human GRCh38 chr17: 42,673,883-42,773,953 , GRCh37.p13 chr17: 40,825,901-40,925,971 VPS25, HMGN2P15, 8 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
    nsv6580573inversion1nstd223human GRCh38 chr17: 42,716,044-42,716,369 , GRCh37.p13 chr17: 40,868,062-40,868,387 EZH1
    nsv6575930inversion1nstd223human GRCh38 chr17: 42,729,758-42,730,796 , GRCh37.p13 chr17: 40,881,776-40,882,814 EZH1
    nsv6512178copy number variation1nstd223human GRCh38 chr17: 42,728,648-42,733,483 , GRCh37.p13 chr17: 40,880,666-40,885,501 EZH1
    nsv6510128copy number variation1nstd223human GRCh38 chr17: 42,726,343-42,726,962 , GRCh37.p13 chr17: 40,878,361-40,878,980 EZH1
    nsv6501288copy number variation1nstd223human GRCh38 chr17: 42,735,992-42,738,147 , GRCh37.p13 chr17: 40,888,010-40,890,165 EZH1
    nsv6310383copy number variation1nstd102humanPathogenic GRCh37 chr17: 40,834,848-40,850,928 , GRCh38.p12 chr17: 42,682,830-42,698,910 EZH1, CNTNAP1
    nsv6137184translocation1nstd213human GRCh37 chr17: 40,883,146-40,883,146 , GRCh38.p12 chr17: 42,731,128-42,731,128 , GRCh38.p12 chr13: 95,165,466-95,165,466 , GRCh37 chr13: 95,817,720-95,817,720 EZH1, ABCC4
    nsv6133246copy number variation1nstd213human GRCh37 chr17: 40,670,000-41,570,001 , GRCh38.p12 chr17: 42,517,982-43,492,633 AOC2, ARL4D, 65 more genes
    nsv6133061copy number variation1nstd213human GRCh37 chr17: 39,870,000-40,890,001 , GRCh38.p12 chr17: 41,713,748-42,737,983 ACLY, ATP6V0A1, 51 more genes
    nsv6133060copy number variation1nstd213human GRCh37 chr17: 39,870,000-40,880,001 , GRCh38.p12 chr17: 41,713,748-42,727,983 ACLY, ATP6V0A1, 51 more genes
    nsv5943431copy number variation1nstd209human GRCh38 chr17: 42,733,435-42,736,629 , GRCh37.p13 chr17: 40,885,453-40,888,647 EZH1
    nsv5942193copy number variation1nstd209human GRCh38 chr17: 42,738,703-42,739,006 , GRCh37.p13 chr17: 40,890,721-40,891,024 EZH1
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