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Items: 1 to 20 of 398

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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
    nsv7093389copy number variation1nstd102humanUncertain significance GRCh37 chr10: 46,584,432-51,974,628 , GRCh38.p12 chr10: 45,931,517-50,214,868 NCOA4, AGAP7P, 106 more genes
    nsv7074782inversion1nstd229human GRCh38 chr10: 48,229,732-48,237,165 , GRCh37.p13 chr10: 49,437,775-49,445,208 FRMPD2
    nsv7069878inversion1nstd229human GRCh38 chr10: 47,497,713-51,210,711 , GRCh37.p13 chr10: 46,591,857-52,970,471 MIR4294, SLC18A3, 76 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
    nsv7060309inversion1nstd229human GRCh38 chr10: 46,173,677-55,799,586 , GRCh37.p13 chr10: 46,591,857-57,559,346 NPY4R, LOC102724603, 138 more genes
    nsv6897342copy number variation1nstd229human GRCh38 chr10: 48,211,546-48,218,110 , GRCh37.p13 chr10: 49,419,589-49,426,153 FRMPD2
    nsv6897068copy number variation1nstd229human GRCh38 chr10: 48,229,601-48,242,900 , GRCh37.p13 chr10: 49,437,644-49,450,943 FRMPD2
    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
    nsv6895527copy number variation1nstd229human GRCh38 chr10: 48,253,666-48,256,922 , GRCh37.p13 chr10: 49,461,709-49,464,965 FRMPD2
    nsv6894901copy number variation1nstd229human GRCh38 chr10: 48,220,001-48,222,200 , GRCh37.p13 chr10: 49,428,044-49,430,243 FRMPD2
    nsv6888343copy number variation1nstd229human GRCh38 chr10: 48,186,904-48,186,943 , GRCh37.p13 chr10: 49,394,947-49,394,986 FRMPD2
    nsv6886950copy number variation1nstd229human GRCh38 chr10: 48,273,811-48,273,835 , GRCh37.p13 chr10: 49,481,854-49,481,878 FRMPD2
    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
    nsv6884284copy number variation1nstd229human GRCh38 chr10: 48,264,901-48,266,300 , GRCh37.p13 chr10: 49,472,944-49,474,343 FRMPD2
    nsv6880330copy number variation1nstd229human GRCh38 chr10: 48,223,335-48,229,457 , GRCh37.p13 chr10: 49,431,378-49,437,500 FRMPD2
    nsv6880020copy number variation1nstd229human GRCh38 chr10: 48,273,340-48,279,913 , GRCh37.p13 chr10: 49,481,383-49,487,956 FRMPD2
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