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Items: 1 to 20 of 160

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5487541copy number variation1nstd206human GRCh38 chr10: 45,150,187-45,157,637 , GRCh37.p13 chr10: 45,645,635-45,653,085 RSU1P2, ANKRD30BP3, 1 more genes
    nsv5478789copy number variation1nstd206human GRCh38 chr10: 45,130,871-45,130,929 , GRCh37.p13 chr10: 45,626,319-45,626,377 CUBNP3, RSU1P2
    nsv5364902translocation1nstd200human GRCh38 chr10: 45,145,576-45,145,576 , GRCh38 chr10: 45,143,726-45,143,726 , GRCh37.p13 chr10: 45,639,174-45,639,174 , GRCh37.p13 chr10: 45,641,024-45,641,024 CUBNP3, RSU1P2
    nsv5347618translocation1nstd200human GRCh38 chr10: 45,130,929-45,130,929 , GRCh38 chr10: 45,130,871-45,130,871 , GRCh37.p13 chr10: 45,626,377-45,626,377 , GRCh37.p13 chr10: 45,626,319-45,626,319 CUBNP3, RSU1P2
    nsv5121118mobile element insertion1nstd203human GRCh38 chr10: 45,125,167-45,125,178 , GRCh37.p13 chr10: 45,620,615-45,620,626 RSU1P2
    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
    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
    nsv4870857inversion1nstd200human GRCh37 chr10: 37,108,081-60,078,188 , GRCh38.p12 chr10: 36,819,153-58,318,428 , NCOA4, 306 more genes
    nsv4835879copy number variation1nstd200human GRCh37 chr10: 45,626,319-45,626,377 , GRCh38.p12 chr10: 45,130,871-45,130,929 RSU1P2, CUBNP3
    nsv4608626copy number variation1nstd183human GRCh37 chr10: 45,603,936-45,641,664 , GRCh38.p12 chr10: 45,108,488-45,146,216 RSU1P2, CUBNP3
    nsv4487062mobile element insertion1nstd166human GRCh37.p13 chr10: 45,620,667-45,620,667 , GRCh38.p12 chr10: 45,125,219-45,125,219 RSU1P2
    nsv4482108mobile element insertion1nstd166human GRCh37.p13 chr10: 45,620,615-45,620,615 , GRCh38.p12 chr10: 45,125,167-45,125,167 RSU1P2
    nsv4426622copy number variation1nstd174human GRCh37 chr10: 45,598,715-45,657,182 , GRCh38.p12 chr10: 45,103,267-45,161,734 RSU1P2, ANKRD54P1, 2 more genes
    nsv4382458copy number variation1nstd173human GRCh37 chr10: 45,603,657-45,641,681 , GRCh38.p12 chr10: 45,108,209-45,146,233 RSU1P2, CUBNP3
    nsv4343722sequence alteration1nstd166human GRCh37.p13 chr10: 43,905,894-92,001,956 , GRCh38.p12 chr10: 43,410,446-90,242,199 , ALOX5, 749 more genes
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