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Items: 1 to 20 of 209

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7071643inversion1nstd229human GRCh38 chr10: 42,146,783-43,722,055 , GRCh37.p13 chr10: 42,642,231-44,217,503 RNU6ATAC11P, EIF3LP2, 48 more genes
    nsv6896735copy number variation1nstd229human GRCh38 chr10: 43,132,928-43,137,286 , GRCh37.p13 chr10: 43,628,376-43,632,734 CSGALNACT2
    nsv6885128copy number variation1nstd229human GRCh38 chr10: 43,146,054-43,150,526 , GRCh37.p13 chr10: 43,641,502-43,645,974 CSGALNACT2
    nsv6884373copy number variation1nstd229human GRCh38 chr10: 43,179,550-43,179,897 , GRCh37.p13 chr10: 43,674,998-43,675,345 CSGALNACT2
    nsv6883580copy number variation1nstd229human GRCh38 chr10: 42,792,424-46,796,570 , GRCh37.p13 chr10: 43,287,872-46,224,333 RASSF4, AGAP14P, 107 more genes
    nsv6455403copy number variation1nstd223human GRCh38 chr10: 43,165,790-43,181,883 , GRCh37.p13 chr10: 43,661,238-43,677,331 CSGALNACT2
    nsv6454231copy number variation1nstd223human GRCh38 chr10: 43,132,927-43,137,285 , GRCh37.p13 chr10: 43,628,375-43,632,733 CSGALNACT2
    nsv6290893copy number variation1nstd102humannot provided GRCh37 chr10: 135,655-47,688,677 , GRCh38.p12 chr10: 89,715-47,923,579 C1QL3, LOC105376441, 774 more genes
    nsv6240614mobile element insertion1nstd215human GRCh38 chr10: 43,146,989-43,146,989 , GRCh37.p13 chr10: 43,642,437-43,642,437 CSGALNACT2
    nsv6095663insertion1nstd212human GRCh38 chr10: 43,181,881-43,181,881 , GRCh37.p13 chr10: 43,677,329-43,677,329 CSGALNACT2
    nsv6009496copy number variation1nstd212human GRCh38 chr10: 43,138,232-43,138,430 , GRCh37.p13 chr10: 43,633,680-43,633,878 CSGALNACT2
    nsv6003243copy number variation1nstd212human GRCh38 chr10: 43,140,301-43,140,359 , GRCh37.p13 chr10: 43,635,749-43,635,807 CSGALNACT2
    nsv5962220insertion1nstd209human GRCh38 chr10: 43,181,881-43,181,881 , GRCh37.p13 chr10: 43,677,329-43,677,329 CSGALNACT2
    nsv5709542mobile element insertion1nstd211human GRCh38 chr10: 43,144,635-43,144,635 , GRCh37.p13 chr10: 43,640,083-43,640,083 CSGALNACT2
    nsv5639874insertion1nstd207human GRCh38 chr10: 43,181,881-43,181,881 , GRCh37.p13 chr10: 43,677,329-43,677,329 CSGALNACT2
    nsv5537774insertion1nstd206human GRCh38 chr10: 43,167,355-43,167,404 , GRCh37.p13 chr10: 43,662,803-43,662,852 CSGALNACT2
    nsv5491892copy number variation1nstd206human GRCh38 chr10: 43,165,005-43,165,728 , GRCh37.p13 chr10: 43,660,453-43,661,176 CSGALNACT2
    nsv5488304copy number variation1nstd206human GRCh38 chr10: 43,129,838-43,138,035 , GRCh37.p13 chr10: 43,625,286-43,633,483 RET, CSGALNACT2
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