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Items: 1 to 20 of 104

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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
    nsv7068595inversion1nstd229human GRCh38 chr10: 45,208,870-45,507,407 , GRCh37.p13 chr10: 45,704,318-46,002,855 ALOX5, OR6D1P, 6 more genes
    nsv7060234inversion1nstd229human GRCh38 chr10: 45,095,166-45,498,206 , GRCh37.p13 chr10: 45,590,614-45,993,654 ALOX5, ANKRD30BP3, 12 more genes
    nsv6895939copy number variation1nstd229human GRCh38 chr10: 45,305,918-45,310,076 , GRCh37.p13 chr10: 45,801,366-45,805,524 OR13A1
    nsv6895651copy number variation1nstd229human GRCh38 chr10: 44,205,517-45,550,271 , GRCh37.p13 chr10: 44,700,965-46,045,719 OR13A1, RPL9P21, 27 more genes
    nsv6884631copy number variation1nstd229human GRCh38 chr10: 45,304,665-45,313,764 , GRCh37.p13 chr10: 45,800,113-45,809,212 OR13A1
    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
    nsv6882722copy number variation1nstd229human GRCh38 chr10: 45,286,474-45,554,400 , GRCh37.p13 chr10: 45,781,922-46,049,848 ALOX5, OR13A1, 3 more genes
    nsv6620136copy number variation1nstd224human GRCh37 chr10: 45,736,244-45,818,114 , GRCh38.p12 chr10: 45,240,796-45,322,666 , GRCh38.p12 chr10|NW_003315935.1: 65,564-147,437 CUBNP2, OR6D1P, 1 more genes
    nsv6290893copy number variation1nstd102humannot provided GRCh37 chr10: 135,655-47,688,677 , GRCh38.p12 chr10: 89,715-47,923,579 C1QL3, LOC105376441, 774 more genes
    nsv5364903translocation1nstd200human GRCh38 chr19: 40,393,768-40,393,768 , GRCh38 chr10: 45,306,959-45,306,959 , GRCh37.p13 chr19: 40,899,675-40,899,675 , GRCh37.p13 chr10: 45,802,407-45,802,407 PRX, OR13A1
    nsv5354398translocation1nstd200human GRCh38 chr19: 40,394,435-40,394,435 , GRCh38 chr10: 45,306,960-45,306,960 , GRCh37.p13 chr10: 45,802,408-45,802,408 , GRCh37.p13 chr19: 40,900,342-40,900,342 OR13A1, PRX
    nsv5035636inversion1nstd200human GRCh38 chr10: 32,580,256-50,959,654 , GRCh37.p13 chr10: 32,869,184-52,719,414 , ZNF32-AS2, 320 more genes
    nsv5033632inversion1nstd200human GRCh38 chr10: 36,819,152-58,318,428 , GRCh37.p13 chr10: 37,108,080-60,078,188 , LOC107001062, 306 more genes
    nsv4973597copy number variation1nstd200human GRCh38 chr10: 45,298,388-45,329,645 , GRCh37.p13 chr10: 45,793,836-45,825,093 OR13A1
    nsv4973589copy number variation1nstd200human GRCh38 chr10: 44,650,256-45,337,855 , GRCh37.p13 chr10: 45,145,704-45,833,303 LOC105378281, OR13A1, 19 more genes
    nsv4969842copy number variation1nstd200human GRCh38 chr10: 45,303,325-45,303,577 , GRCh37.p13 chr10: 45,798,773-45,799,025 OR13A1
    nsv4870857inversion1nstd200human GRCh37 chr10: 37,108,081-60,078,188 , GRCh38.p12 chr10: 36,819,153-58,318,428 , NCOA4, 306 more genes
    nsv4769357copy number variation1nstd102humanUncertain significance GRCh37 chr10: 45,758,657-46,021,583 , GRCh38.p12 chr10|NW_003315935.1: 87,977-309,802 , GRCh38.p12 chr10: 45,263,209-45,526,135 ALOX5, OR13A1, 3 more genes
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