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Items: 1 to 20 of 174

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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
    nsv7098865copy number variation1nstd102humanLikely pathogenic GRCh37.p13 chr10|NW_003871068.1: 1-2,281,126 , GRCh38 chr10: 45,704,708-50,015,268 , GRCh37.p13 chr10: 46,200,156-51,028,871 CHAT, CTSLP2, 107 more genes
    nsv7073680inversion1nstd229human GRCh38 chr10: 45,636,033-46,089,424 , GRCh37.p13 chr10|NW_003871068.1: 1-360,539 RPL35AP23, AGAP4, 15 more genes
    nsv7073382inversion1nstd229human GRCh38 chr10: 45,705,380-45,807,586 , GRCh37.p13 chr10: 46,224,334-46,303,034 , GRCh37.p13 chr10|NW_003871068.1: 1-78,701 FAM21FP, LOC107984227, 1 more genes
    nsv7071738inversion1nstd229human GRCh38 chr10: 45,701,670-45,732,363 , GRCh37.p13 chr10: 46,197,118-46,224,333 WASHC2C, LOC107984227, 1 more genes
    nsv7064671inversion1nstd229human GRCh38 chr10: 45,585,629-45,848,646 , GRCh37.p13 chr10: 46,081,077-46,224,333 FAM25EP, FAM21FP, 7 more genes
    nsv6896922copy number variation1nstd229human GRCh38 chr10: 45,717,647-46,044,684 , GRCh37.p13 chr10|NW_003871068.1: 1-315,799 PARGP1-AGAP4, RPL35AP23, 12 more genes
    nsv6886834copy number variation1nstd229human GRCh38 chr10: 45,568,878-51,464,891 , GRCh37.p13 chr10: 46,064,326-53,224,651 PGBD3, MAPK8, 134 more genes
    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
    nsv6593670inversion1nstd223human GRCh37.p13 chr10|NW_003871068.1: 1-71,951 , GRCh38 chr10: 45,667,229-45,800,836 , GRCh37.p13 chr10: 46,224,334-46,296,284 ZFAND4, WASHC2C, 3 more genes
    nsv6445453copy number variation1nstd223human GRCh38 chr10: 45,725,201-45,727,700 , GRCh37.p13 chr10: 46,220,649-46,223,148 WASHC2C, LOC107984227
    nsv6290893copy number variation1nstd102humannot provided GRCh37 chr10: 135,655-47,688,677 , GRCh38.p12 chr10: 89,715-47,923,579 C1QL3, LOC105376441, 774 more genes
    nsv6290803copy number variation1nstd102humanLikely benign GRCh37 chr10: 46,189,526-46,293,591 , GRCh38.p12 chr10: 45,694,078-45,798,143 LOC107984227, FAM21FP, 2 more genes
    nsv6290115copy number variation1nstd218human GRCh38.p12 chr10: 45,674,369-47,923,579 , GRCh37 chr10: 46,169,817-47,702,587 , CTSLP2, 71 more genes
    nsv6290114copy number variation1nstd218human GRCh38.p12 chr10: 45,662,649-47,923,579 , GRCh37 chr10: 46,158,097-47,702,587 , CTSLP2, 72 more genes
    nsv6143289copy number variation1nstd206human GRCh38 chr10: 45,704,265-45,734,265 , GRCh37.p13 chr10: 46,199,713-46,224,333 WASHC2C, FAM21FP, 1 more genes
    nsv6143175copy number variation1nstd206human GRCh38 chr10: 45,724,000-45,736,265 , GRCh37.p13 chr10: 46,224,334-46,231,713 , GRCh37.p13 chr10|NW_003871068.1: 1-7,380 LOC107984227, WASHC2C
    nsv5864602copy number variation1nstd209human GRCh38 chr10: 45,726,944-45,733,579 , GRCh37.p13 chr10: 46,224,334-46,229,027 , GRCh37.p13 chr10|NW_003871068.1: 1-4,694 LOC107984227, WASHC2C
    nsv5850967copy number variation1nstd209human GRCh38 chr10: 45,723,708-45,727,165 , GRCh37.p13 chr10: 46,219,156-46,222,613 WASHC2C, LOC107984227, 1 more genes
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