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Items: 1 to 20 of 152

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147208copy number variation1nstd232human GRCh37.p13 chr7: 26,681,315-26,681,396 , GRCh38.p12 chr7: 26,641,696-26,641,777 LINC02860
    nsv7043886inversion1nstd229human GRCh38 chr7: 25,072,526-28,462,757 , GRCh37.p13 chr7: 25,112,145-28,502,375 HOXA3, CREB5, 72 more genes
    nsv6810450copy number variation1nstd229human GRCh38 chr7: 26,639,161-26,642,978 , GRCh37.p13 chr7: 26,678,780-26,682,597 LINC02860
    nsv6806392copy number variation1nstd229human GRCh38 chr7: 26,630,229-26,636,455 , GRCh37.p13 chr7: 26,669,848-26,676,074 LINC02860
    nsv6804127copy number variation1nstd229human GRCh38 chr7: 26,634,571-26,679,624 , GRCh37.p13 chr7: 26,674,190-26,719,243 SKAP2, LINC02860
    nsv6800550copy number variation1nstd229human GRCh38 chr7: 26,646,801-26,651,700 , GRCh37.p13 chr7: 26,686,420-26,691,319 LINC02860
    nsv6636197copy number variation1nstd102humanUncertain significance GRCh37 chr7: 26,418,391-28,323,299 , GRCh38.p12 chr7: 26,378,771-28,283,680 LINC02860, LINC03095, 49 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6616063copy number variation1nstd223human GRCh38 chr7: 26,646,745-26,651,733 , GRCh37.p13 chr7: 26,686,364-26,691,352 LINC02860
    nsv6562857inversion1nstd223human GRCh38 chr7: 26,639,896-26,642,620 , GRCh37.p13 chr7: 26,679,515-26,682,239 LINC02860
    nsv6562499inversion1nstd223human GRCh38 chr7: 25,072,527-28,462,755 , GRCh37.p13 chr7: 25,112,146-28,502,373 HOXA10-AS, HOXA2, 72 more genes
    nsv6315453copy number variation1nstd102humanPathogenic GRCh37 chr7: 25,451,740-33,864,069 , GRCh38.p12 chr7: 25,412,121-33,824,457 PLEKHA8, NFE2L3, 141 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313591copy number variation1nstd102humanUncertain significance GRCh37 chr7: 26,270,121-27,193,008 , GRCh38.p12 chr7: 26,230,501-27,153,389 HOXA1, RPL23P7, 22 more genes
    nsv6313493copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 10,745,750-35,305,167 , GRCh38.p12 chr7: 10,706,123-35,265,556 ADCYAP1R1, AHR, 329 more genes
    nsv6268151copy number variation1nstd214human GRCh38 chr7: 26,641,708-26,641,780 , GRCh37.p13 chr7: 26,681,327-26,681,399 LINC02860
    nsv6267391copy number variation1nstd214human GRCh38 chr7: 26,641,696-26,641,777 , GRCh37.p13 chr7: 26,681,315-26,681,396 LINC02860
    nsv6187470copy number variation1nstd214human GRCh38 chr7: 26,641,711-26,641,777 , GRCh37.p13 chr7: 26,681,330-26,681,396 LINC02860
    nsv6177455copy number variation1nstd214human GRCh38 chr7: 26,641,727-26,641,778 , GRCh37.p13 chr7: 26,681,346-26,681,397 LINC02860
    nsv6176262copy number variation1nstd214human GRCh38 chr7: 26,641,683-26,641,777 , GRCh37.p13 chr7: 26,681,302-26,681,396 LINC02860
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