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Items: 1 to 20 of 415

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094921copy number variation1nstd102humanUncertain significance GRCh37 chr17: 76,851,749-78,367,298 , GRCh38.p12 chr17: 78,855,667-80,393,498 RNF213-AS1, EIF4A3, 25 more genes
    nsv7072983inversion1nstd229human GRCh38 chr17: 79,606,852-81,315,890 , GRCh37.p13 chr17: 77,766,017-79,289,690 MIR4739, MIR4730, 44 more genes
    nsv7071296inversion1nstd229human GRCh38 chr17: 79,045,634-82,531,412 , GRCh37.p13 chr17: 77,041,716-80,489,288 , ENPP7, 111 more genes
    nsv7070005inversion1nstd229human GRCh38 chr17: 80,392,336-80,392,389 , GRCh37.p13 chr17: 78,366,136-78,366,189 RNF213, RNF213-AS1
    nsv7067212inversion1nstd229human GRCh38 chr17: 79,320,851-81,127,081 , GRCh37.p13 chr17: 77,316,933-79,100,881 RPL32P31, RPTOR, 35 more genes
    nsv7065384inversion1nstd229human GRCh38 chr17: 79,173,003-81,030,493 , GRCh37.p13 chr17: 77,169,085-79,004,293 GAA, ENPP7, 30 more genes
    nsv7061803inversion1nstd229human GRCh38 chr17: 79,169,515-81,031,248 , GRCh37.p13 chr17: 77,165,597-79,005,048 CBX4, SLC26A11, 30 more genes
    nsv6995125copy number variation1nstd229human GRCh38 chr17: 80,415,278-80,419,910 , GRCh37.p13 chr17: 78,389,078-78,393,710 ENDOV, MIR4730, 1 more genes
    nsv6993950copy number variation1nstd229human GRCh38 chr17: 80,247,463-80,351,459 , GRCh37.p13 chr17: 78,221,262-78,325,259 RNF213, SLC26A11, 1 more genes
    nsv6993667copy number variation1nstd229human GRCh38 chr17: 78,709,580-81,173,842 , GRCh37.p13 chr17: 76,705,662-79,147,642 C1QTNF1-AS1, NPTX1, 47 more genes
    nsv6992964copy number variation1nstd229human GRCh38 chr17: 80,367,820-80,421,647 , GRCh37.p13 chr17: 78,341,620-78,395,447 RNF213, ENDOV, 2 more genes
    nsv6992816copy number variation1nstd229human GRCh38 chr17: 80,407,175-80,461,708 , GRCh37.p13 chr17: 78,380,975-78,435,508 RNF213-AS1, ENDOV, 1 more genes
    nsv6991318copy number variation1nstd229human GRCh38 chr17: 80,365,518-80,365,547 , GRCh37.p13 chr17: 78,339,318-78,339,347 RNF213, RNF213-AS1
    nsv6989020copy number variation1nstd229human GRCh38 chr17: 80,369,797-80,384,678 , GRCh37.p13 chr17: 78,343,597-78,358,478 RNF213, RNF213-AS1
    nsv6986011copy number variation1nstd229human GRCh38 chr17: 80,406,124-80,412,643 , GRCh37.p13 chr17: 78,379,924-78,386,443 RNF213-AS1
    nsv6980637copy number variation1nstd229human GRCh38 chr17: 80,401,630-80,403,999 , GRCh37.p13 chr17: 78,375,430-78,377,799 RNF213-AS1
    nsv6980415copy number variation1nstd229human GRCh38 chr17: 80,373,661-80,373,788 , GRCh37.p13 chr17: 78,347,461-78,347,588 RNF213, RNF213-AS1
    nsv6978447copy number variation1nstd229human GRCh38 chr17: 80,401,988-80,407,434 , GRCh37.p13 chr17: 78,375,788-78,381,234 RNF213-AS1
    nsv6637686copy number variation1nstd102humanUncertain significance GRCh37 chr17: 78,230,693-79,048,694 , GRCh38.p12 chr17: 80,256,894-81,074,894 RNF213-AS1, RPL31P7, 13 more genes
    nsv6624527copy number variation1nstd224human GRCh37 chr17: 78,367,161-78,397,337 , GRCh38.p12 chr17: 80,393,361-80,423,537 RNF213-AS1, ENDOV, 2 more genes
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