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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
    nsv7070229inversion1nstd229human GRCh38 chr11: 92,451,554-94,033,544 , GRCh37.p13 chr11: 92,184,720-93,766,710 SNORA32, SNORA18, 30 more genes
    nsv7068937inversion1nstd229human GRCh38 chr11: 93,835,064-93,835,142 , GRCh37.p13 chr11: 93,568,230-93,568,308 VSTM5
    nsv7066697inversion1nstd229human GRCh38 chr11: 93,843,933-93,844,337 , GRCh37.p13 chr11: 93,577,099-93,577,503 VSTM5
    nsv7060154inversion1nstd229human GRCh38 chr11: 89,626,991-96,425,689 , GRCh37.p13 chr11: 89,360,159-96,158,853 LINC02756, OSBPL9P2, 119 more genes
    nsv6916581copy number variation1nstd229human GRCh38 chr11: 93,844,838-93,845,047 , GRCh37.p13 chr11: 93,578,004-93,578,213 VSTM5
    nsv6915685copy number variation1nstd229human GRCh38 chr11: 93,826,001-93,833,700 , GRCh37.p13 chr11: 93,559,167-93,566,866 VSTM5
    nsv6914121copy number variation1nstd229human GRCh38 chr11: 89,708,489-94,988,932 , GRCh37.p13 chr11: 89,441,657-94,611,845 SNORA40, PIWIL4-AS1, 89 more genes
    nsv6913968copy number variation1nstd229human GRCh38 chr11: 93,817,022-93,817,127 , GRCh37.p13 chr11: 93,550,188-93,550,293 VSTM5
    nsv6913192copy number variation1nstd229human GRCh38 chr11: 93,809,001-93,815,600 , GRCh37.p13 chr11: 93,542,167-93,548,766 MED17, VSTM5
    nsv6908137copy number variation1nstd229human GRCh38 chr11: 93,820,457-93,820,528 , GRCh37.p13 chr11: 93,553,623-93,553,694 VSTM5
    nsv6908126copy number variation1nstd229human GRCh38 chr11: 93,843,080-93,861,182 , GRCh37.p13 chr11: 93,576,246-93,594,348 VSTM5
    nsv6907347copy number variation1nstd229human GRCh38 chr11: 89,715,432-96,566,090 , GRCh37.p13 chr11: 89,448,600-96,287,584 DISC1FP1, RPL32P25, 120 more genes
    nsv6905227copy number variation1nstd229human GRCh38 chr11: 93,833,598-93,836,546 , GRCh37.p13 chr11: 93,566,764-93,569,712 VSTM5
    nsv6903469copy number variation1nstd229human GRCh38 chr11: 93,818,367-93,934,635 , GRCh37.p13 chr11: 93,551,533-93,667,801 LOC101060084, VSTM5
    nsv6900323copy number variation1nstd229human GRCh38 chr11: 93,200,748-96,340,159 , GRCh37.p13 chr11: 92,933,914-96,073,323 FGFR3P2, LOC112268080, 67 more genes
    nsv6898454copy number variation1nstd229human GRCh38 chr11: 93,836,601-93,840,300 , GRCh37.p13 chr11: 93,569,767-93,573,466 VSTM5
    nsv6637396copy number variation1nstd102humanPathogenic GRCh37 chr11: 81,478,509-104,667,040 , GRCh38.p12 chr11: 81,767,467-104,796,313 LOC107984375, RN7SL222P, 295 more genes
    nsv6593696inversion1nstd223human GRCh38 chr11: 93,826,088-93,826,590 , GRCh37.p13 chr11: 93,559,254-93,559,756 VSTM5
    nsv6459070copy number variation1nstd223human GRCh38 chr11: 92,156,862-95,481,795 , GRCh37.p13 chr11: 91,890,028-95,214,959 FUT4, KDM4D, 66 more genes
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
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