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Items: 1 to 20 of 322

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148121copy number variation1nstd102humanPathogenic GRCh37 chr10: 46,284,269-51,870,080 , GRCh38.p12 chr10: 45,788,821-50,110,320 LOC100420617, ZNF488, 108 more genes
    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
    nsv7066519inversion1nstd229human GRCh38 chr10: 45,802,941-50,026,843 , GRCh37.p13 chr10|NW_003871068.1: 74,056-2,281,126 , GRCh37.p13 chr10: 46,591,857-51,028,871 RNA5SP317, AHCYP1, 106 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
    nsv6895769copy number variation1nstd229human GRCh38 chr10: 45,735,504-50,076,220 , GRCh37.p13 chr10: 46,591,857-51,028,871 , GRCh37.p13 chr10|NW_003871068.1: 6,619-2,281,126 BMS1P1, AGAP9, 108 more genes
    nsv6894919copy number variation1nstd229human GRCh38 chr10: 45,805,501-45,829,400 , GRCh37.p13 chr10|NW_003871068.1: 76,616-100,515 FAM25EP, AGAP4, 1 more genes
    nsv6894011copy number variation1nstd229human GRCh38 chr10: 45,806,601-45,829,400 , GRCh37.p13 chr10|NW_003871068.1: 77,716-100,515 AGAP4, PARGP1-AGAP4, 1 more genes
    nsv6890551copy number variation1nstd229human GRCh38 chr10: 45,831,001-45,954,700 , GRCh37.p13 chr10|NW_003871068.1: 102,116-225,815 AGAP4, PARGP1-AGAP4, 3 more genes
    nsv6889830copy number variation1nstd229human GRCh38 chr10: 45,805,101-45,829,400 , GRCh37.p13 chr10|NW_003871068.1: 76,216-100,515 FAM25EP, PARGP1-AGAP4, 1 more genes
    nsv6889356copy number variation1nstd229human GRCh38 chr10: 45,848,901-45,856,100 , GRCh37.p13 chr10|NW_003871068.1: 120,016-127,215 AGAP4, PARGP1-AGAP4, 2 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
    nsv6884193copy number variation1nstd229human GRCh38 chr10: 45,847,901-45,965,200 , GRCh37.p13 chr10|NW_003871068.1: 119,016-236,315 RNA5SP310, RPL35AP23, 3 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
    nsv6637283copy number variation1nstd102humanLikely pathogenic GRCh37 chr10: 46,269,493-51,874,356 , GRCh38.p12 chr10: 45,774,045-50,114,596 CHAT, CTSLP2, 108 more genes
    nsv6635526copy number variation2nstd227human GRCh38.p12 chr10: 45,788,238-47,923,579 , GRCh37 chr10: 46,283,686-47,703,869 CTSLP2, GDF2, 65 more genes
    nsv6634443copy number variation1nstd102humanPathogenic GRCh37 chr10: 46,287,821-51,627,470 , GRCh38.p12 chr10: 45,792,373-49,929,364 GLUD1P2, RBP3, 100 more genes
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