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Items: 1 to 20 of 282

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7138639copy number variation1nstd232human GRCh37.p13 chr10: 43,960,566-43,960,614 , GRCh38.p12 chr10: 43,465,118-43,465,166 ZNF487
    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
    nsv7071643inversion1nstd229human GRCh38 chr10: 42,146,783-43,722,055 , GRCh37.p13 chr10: 42,642,231-44,217,503 RNU6ATAC11P, EIF3LP2, 48 more genes
    nsv7070944inversion1nstd229human GRCh38 chr10: 43,424,046-43,446,081 , GRCh37.p13 chr10: 43,919,494-43,941,529 ZNF487
    nsv7061966inversion1nstd229human GRCh38 chr10: 43,416,777-43,460,853 , GRCh37.p13 chr10: 43,912,225-43,956,301 RNU7-193P, SNORD3J, 1 more genes
    nsv7059052inversion1nstd229human GRCh38 chr10: 43,416,771-43,460,852 , GRCh37.p13 chr10: 43,912,219-43,956,300 ZNF487, RNU7-193P, 1 more genes
    nsv6897414copy number variation1nstd229human GRCh38 chr10: 43,436,853-43,437,098 , GRCh37.p13 chr10: 43,932,301-43,932,546 ZNF487
    nsv6894163copy number variation1nstd229human GRCh38 chr10: 43,430,751-43,437,819 , GRCh37.p13 chr10: 43,926,199-43,933,267 ZNF487
    nsv6892040copy number variation1nstd229human GRCh38 chr10: 43,479,174-43,479,744 , GRCh37.p13 chr10: 43,974,622-43,975,192 ZNF487
    nsv6891534copy number variation1nstd229human GRCh38 chr10: 43,482,916-43,587,800 , GRCh37.p13 chr10: 43,978,364-44,083,248 LOC100130881, ZNF239, 1 more genes
    nsv6888815copy number variation1nstd229human GRCh38 chr10: 43,410,264-43,462,953 , GRCh37.p13 chr10: 43,905,712-43,958,401 ZNF487, SNORD3J, 1 more genes
    nsv6887551copy number variation1nstd229human GRCh38 chr10: 43,244,701-43,469,100 , GRCh37.p13 chr10: 43,740,149-43,964,548 LOC107984226, RASGEF1A, 8 more genes
    nsv6885382copy number variation1nstd229human GRCh38 chr10: 43,462,879-43,467,058 , GRCh37.p13 chr10: 43,958,327-43,962,506 ZNF487
    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
    nsv6881182copy number variation1nstd229human GRCh38 chr10: 43,432,677-43,449,682 , GRCh37.p13 chr10: 43,928,125-43,945,130 ZNF487
    nsv6880282copy number variation1nstd229human GRCh38 chr10: 43,460,573-43,460,621 , GRCh37.p13 chr10: 43,956,021-43,956,069 ZNF487
    nsv6879994copy number variation1nstd229human GRCh38 chr10: 43,472,469-43,472,679 , GRCh37.p13 chr10: 43,967,917-43,968,127 ZNF487
    nsv6878778copy number variation1nstd229human GRCh38 chr10: 43,457,793-43,467,588 , GRCh37.p13 chr10: 43,953,241-43,963,036 RNU7-193P, ZNF487
    nsv6878301copy number variation1nstd229human GRCh38 chr10: 43,432,139-43,541,039 , GRCh37.p13 chr10: 43,927,587-44,036,487 ZNF487, RNU7-193P, 1 more genes
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