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Items: 1 to 20 of 176

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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
    nsv7060234inversion1nstd229human GRCh38 chr10: 45,095,166-45,498,206 , GRCh37.p13 chr10: 45,590,614-45,993,654 ALOX5, ANKRD30BP3, 12 more genes
    nsv6897503copy number variation1nstd229human GRCh38 chr10: 45,152,895-45,153,454 , GRCh37.p13 chr10: 45,648,343-45,648,902 RSU1P2, ANKRD30BP3
    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
    nsv6894645copy number variation1nstd229human GRCh38 chr10: 45,109,035-45,109,614 , GRCh37.p13 chr10: 45,604,483-45,605,062 RSU1P2
    nsv6894442copy number variation1nstd229human GRCh38 chr10: 45,073,401-45,104,600 , GRCh37.p13 chr10: 45,568,849-45,600,048 RPS19P7, RSU1P2
    nsv6891675copy number variation1nstd229human GRCh38 chr10: 45,106,284-45,154,798 , GRCh37.p13 chr10: 45,601,732-45,650,246 ANKRD30BP3, ANKRD54P1, 2 more genes
    nsv6890479copy number variation1nstd229human GRCh38 chr10: 45,053,742-45,109,775 , GRCh37.p13 chr10: 45,549,190-45,605,223 RPS19P7, CEP164P1, 2 more genes
    nsv6887530copy number variation1nstd229human GRCh38 chr10: 45,105,666-45,147,080 , GRCh37.p13 chr10: 45,601,114-45,642,528 CUBNP3, RSU1P2
    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
    nsv6883029copy number variation1nstd229human GRCh38 chr10: 45,095,152-45,100,797 , GRCh37.p13 chr10: 45,590,600-45,596,245 RSU1P2
    nsv6882959copy number variation1nstd229human GRCh38 chr10: 45,130,871-45,130,929 , GRCh37.p13 chr10: 45,626,319-45,626,377 RSU1P2, CUBNP3
    nsv6590999inversion1nstd223human GRCh38 chr10: 45,113,849-45,114,445 , GRCh37.p13 chr10: 45,609,297-45,609,893 RSU1P2
    nsv6448066copy number variation1nstd223human GRCh38 chr10: 45,150,969-45,151,445 , GRCh37.p13 chr10: 45,646,417-45,646,893 RSU1P2, ANKRD54P1
    nsv6290893copy number variation1nstd102humannot provided GRCh37 chr10: 135,655-47,688,677 , GRCh38.p12 chr10: 89,715-47,923,579 C1QL3, LOC105376441, 774 more genes
    nsv5627401insertion1nstd207human GRCh38 chr10: 45,112,681-45,112,681 , GRCh37.p13 chr10: 45,608,129-45,608,129 RSU1P2
    nsv5602166copy number variation1nstd207human GRCh38 chr10: 45,107,705-45,107,764 , GRCh37.p13 chr10: 45,603,153-45,603,212 RSU1P2
    nsv5599880copy number variation1nstd207human GRCh38 chr10: 45,109,009-45,109,304 , GRCh37.p13 chr10: 45,604,457-45,604,752 RSU1P2
    nsv5493841copy number variation1nstd206human GRCh38 chr10: 45,106,119-45,106,476 , GRCh37.p13 chr10: 45,601,567-45,601,924 RSU1P2
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