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Items: 1 to 20 of 326

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7064787inversion1nstd229human GRCh38 chr13: 70,135,597-70,135,623 , GRCh37.p13 chr13: 70,709,729-70,709,755 ATXN8OS
    nsv6957080copy number variation1nstd229human GRCh38 chr13: 70,119,025-70,135,302 , GRCh37.p13 chr13: 70,693,157-70,709,434 ATXN8OS
    nsv6956728copy number variation1nstd229human GRCh38 chr13: 70,033,601-70,136,000 , GRCh37.p13 chr13: 70,607,733-70,710,132 LUC7L3P1, KLHL1, 1 more genes
    nsv6951759copy number variation1nstd229human GRCh38 chr13: 70,087,588-70,897,297 , GRCh37.p13 chr13: 70,661,720-71,471,429 LOC105370255, ATXN8OS, 3 more genes
    nsv6951426copy number variation1nstd229human GRCh38 chr13: 70,079,282-70,219,607 , GRCh37.p13 chr13: 70,653,414-70,793,739 LUC7L3P1, KLHL1, 1 more genes
    nsv6949524copy number variation1nstd229human GRCh38 chr13: 70,127,123-70,160,000 , GRCh37.p13 chr13: 70,701,255-70,734,132 ATXN8OS
    nsv6946548copy number variation1nstd229human GRCh38 chr13: 69,999,075-71,028,657 , GRCh37.p13 chr13: 70,573,207-71,602,789 RNU6-54P, ATXN8OS, 5 more genes
    nsv6945714copy number variation1nstd229human GRCh38 chr13: 70,131,533-70,136,236 , GRCh37.p13 chr13: 70,705,665-70,710,368 ATXN8OS
    nsv6944617copy number variation1nstd229human GRCh38 chr13: 70,133,116-70,133,307 , GRCh37.p13 chr13: 70,707,248-70,707,439 ATXN8OS
    nsv6942783copy number variation1nstd229human GRCh38 chr13: 70,137,120-70,143,809 , GRCh37.p13 chr13: 70,711,252-70,717,941 ATXN8OS
    nsv6938660copy number variation1nstd229human GRCh38 chr13: 70,005,775-70,124,427 , GRCh37.p13 chr13: 70,579,907-70,698,559 LUC7L3P1, KLHL1, 1 more genes
    nsv6634431copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,253,848-115,108,937 , GRCh38.p12 chr13: 18,679,708-114,343,462 MTUS2-AS1, LOC105370213, 1330 more genes
    nsv6622323copy number variation1nstd224human GRCh37 chr13: 70,397,216-71,165,763 , GRCh38.p12 chr13: 69,823,084-70,591,631 ATXN8OS, KLHL1, 4 more genes
    nsv6494601copy number variation1nstd223human GRCh38 chr13: 70,079,282-70,219,604 , GRCh37.p13 chr13: 70,653,414-70,793,736 ATXN8OS, LUC7L3P1, 1 more genes
    nsv6484026copy number variation1nstd223human GRCh38 chr13: 69,999,075-71,028,657 , GRCh37.p13 chr13: 70,573,207-71,602,789 MTCL1P1, LUC7L3P1, 5 more genes
    nsv6481160copy number variation1nstd223human GRCh38 chr13: 70,122,301-70,123,100 , GRCh37.p13 chr13: 70,696,433-70,697,232 ATXN8OS
    nsv6480609copy number variation1nstd223human GRCh38 chr13: 70,033,567-70,135,972 , GRCh37.p13 chr13: 70,607,699-70,710,104 ATXN8OS, LUC7L3P1, 1 more genes
    nsv6479927copy number variation1nstd223human GRCh38 chr13: 70,124,832-70,125,424 , GRCh37.p13 chr13: 70,698,964-70,699,556 ATXN8OS
    nsv6315495copy number variation1nstd102humanPathogenic GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403 RNU6-80P, EFNB2, 1334 more genes
    nsv6314117copy number variation1nstd102humanPathogenic GRCh37 chr13: 36,376,204-80,681,753 , GRCh38.p12 chr13: 35,802,067-80,107,618 RBM26, RNY4P31, 591 more genes
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