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Items: 1 to 20 of 630

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7066414inversion1nstd229human GRCh38 chr14: 79,890,342-89,436,638 , GRCh37.p13 chr14: 80,356,685-89,902,982 SPATA7, RNU6ATAC28P, 82 more genes
    nsv7063976inversion1nstd229human GRCh38 chr14: 81,408,266-81,818,439 , GRCh37.p13 chr14: 81,874,610-82,284,783 RPL9P6, EEF1A1P2, 8 more genes
    nsv7063833inversion1nstd229human GRCh38 chr14: 81,302,353-81,302,444 , GRCh37.p13 chr14: 81,768,697-81,768,788 STON2
    nsv7060344inversion1nstd229human GRCh38 chr14: 81,104,679-81,358,991 , GRCh37.p13 chr14: 81,571,023-81,825,335 STON2, LOC105370594, 8 more genes
    nsv6972956copy number variation1nstd229human GRCh38 chr14: 81,364,432-82,133,685 , GRCh37.p13 chr14: 81,830,776-82,600,029 LINC02311, EIF3LP1, 9 more genes
    nsv6972338copy number variation1nstd229human GRCh38 chr14: 81,411,801-81,415,300 , GRCh37.p13 chr14: 81,878,145-81,881,644 STON2, DYNLL1P2
    nsv6972075copy number variation1nstd229human GRCh38 chr14: 81,317,014-81,318,836 , GRCh37.p13 chr14: 81,783,358-81,785,180 STON2
    nsv6968464copy number variation1nstd229human GRCh38 chr14: 81,379,454-81,379,538 , GRCh37.p13 chr14: 81,845,798-81,845,882 STON2
    nsv6967864copy number variation1nstd229human GRCh38 chr14: 81,376,664-81,444,942 , GRCh37.p13 chr14: 81,843,008-81,911,286 DYNLL1P2, LINC02308, 1 more genes
    nsv6967457copy number variation1nstd229human GRCh38 chr14: 81,425,856-81,441,230 , GRCh37.p13 chr14: 81,892,200-81,907,574 LINC02308, STON2
    nsv6966995copy number variation1nstd229human GRCh38 chr14: 81,426,285-81,429,954 , GRCh37.p13 chr14: 81,892,629-81,896,298 STON2
    nsv6966874copy number variation1nstd229human GRCh38 chr14: 81,389,432-81,449,827 , GRCh37.p13 chr14: 81,855,776-81,916,171 DYNLL1P2, LINC02308, 1 more genes
    nsv6966869copy number variation1nstd229human GRCh38 chr14: 81,337,641-81,340,073 , GRCh37.p13 chr14: 81,803,985-81,806,417 STON2
    nsv6965966copy number variation1nstd229human GRCh38 chr14: 81,399,696-81,404,804 , GRCh37.p13 chr14: 81,866,040-81,871,148 STON2
    nsv6965413copy number variation1nstd229human GRCh38 chr14: 81,411,884-81,414,269 , GRCh37.p13 chr14: 81,878,228-81,880,613 DYNLL1P2, STON2
    nsv6964745copy number variation1nstd229human GRCh38 chr14: 81,423,618-81,442,017 , GRCh37.p13 chr14: 81,889,962-81,908,361 STON2, LINC02308
    nsv6964479copy number variation1nstd229human GRCh38 chr14: 81,430,479-81,447,162 , GRCh37.p13 chr14: 81,896,823-81,913,506 STON2, LINC02308
    nsv6963359copy number variation1nstd229human GRCh38 chr14: 81,308,820-81,308,923 , GRCh37.p13 chr14: 81,775,164-81,775,267 STON2
    nsv6962972copy number variation1nstd229human GRCh38 chr14: 81,361,849-81,367,431 , GRCh37.p13 chr14: 81,828,193-81,833,775 STON2
    nsv6961985copy number variation1nstd229human GRCh38 chr14: 81,343,338-81,377,547 , GRCh37.p13 chr14: 81,809,682-81,843,891 STON2
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