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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144049insertion1nstd232human GRCh37.p13 chr10: 119,957,754-119,957,754 , GRCh38.p12 chr10: 118,198,242-118,198,242 CASC2
    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
    nsv7070731inversion1nstd229human GRCh38 chr10: 118,128,093-118,131,382 , GRCh37.p13 chr10: 119,887,604-119,890,893 CASC2
    nsv7063382inversion1nstd229human GRCh38 chr10: 118,139,612-118,169,718 , GRCh37.p13 chr10: 119,899,123-119,929,229 CASC2
    nsv7062678inversion1nstd229human GRCh38 chr10: 118,145,732-118,145,759 , GRCh37.p13 chr10: 119,905,243-119,905,270 CASC2
    nsv7059988inversion1nstd229human GRCh38 chr10: 118,126,624-118,142,276 , GRCh37.p13 chr10: 119,886,135-119,901,787 CASC2
    nsv6894762copy number variation1nstd229human GRCh38 chr10: 118,183,340-118,188,043 , GRCh37.p13 chr10: 119,942,852-119,947,555 CASC2
    nsv6894511copy number variation1nstd229human GRCh38 chr10: 118,143,417-118,149,108 , GRCh37.p13 chr10: 119,902,928-119,908,619 CASC2
    nsv6893015copy number variation1nstd229human GRCh38 chr10: 118,129,285-118,133,130 , GRCh37.p13 chr10: 119,888,796-119,892,641 CASC2
    nsv6892830copy number variation1nstd229human GRCh38 chr10: 117,664,803-118,402,207 , GRCh37.p13 chr10: 119,424,314-120,161,719 RAB11FIP2, FAM204A, 6 more genes
    nsv6891986copy number variation1nstd229human GRCh38 chr10: 118,140,429-118,159,001 , GRCh37.p13 chr10: 119,899,940-119,918,512 CASC2
    nsv6889753copy number variation1nstd229human GRCh38 chr10: 118,065,726-118,069,968 , GRCh37.p13 chr10: 119,825,237-119,829,479 CASC2
    nsv6887196copy number variation1nstd229human GRCh38 chr10: 118,057,801-118,058,800 , GRCh37.p13 chr10: 119,817,312-119,818,311 CASC2
    nsv6887040copy number variation1nstd229human GRCh38 chr10: 118,118,364-118,122,123 , GRCh37.p13 chr10: 119,877,875-119,881,634 CASC2
    nsv6886391copy number variation1nstd229human GRCh38 chr10: 118,193,745-118,196,869 , GRCh37.p13 chr10: 119,953,257-119,956,381 CASC2
    nsv6884917copy number variation1nstd229human GRCh38 chr10: 118,057,240-118,061,734 , GRCh37.p13 chr10: 119,816,751-119,821,245 CASC2
    nsv6883285copy number variation1nstd229human GRCh38 chr10: 118,201,976-118,208,534 , GRCh37.p13 chr10: 119,961,488-119,968,046 CASC2
    nsv6882619copy number variation1nstd229human GRCh38 chr10: 118,159,058-118,163,513 , GRCh37.p13 chr10: 119,918,569-119,923,024 CASC2
    nsv6881035copy number variation1nstd229human GRCh38 chr10: 118,068,212-118,071,347 , GRCh37.p13 chr10: 119,827,723-119,830,858 CASC2
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