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Items: 1 to 20 of 22

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3896202copy number variation1nstd102humanBenign GRCh37 chr10: 31,247,387-31,294,981 , GRCh38.p12 chr10: 30,958,458-31,006,052 ZNF438
    nsv3905296copy number variation1nstd102humanBenign GRCh37 chr10: 31,245,835-31,275,977 , GRCh38.p12 chr10: 30,956,906-30,987,048 ZNF438
    nsv3890026copy number variation1nstd102humanBenign GRCh37 chr10: 31,247,142-31,276,664 , GRCh38.p12 chr10: 30,958,213-30,987,735 ZNF438
    nsv3897764copy number variation1nstd102humanBenign GRCh37 chr10: 31,247,387-31,276,664 , GRCh38.p12 chr10: 30,958,458-30,987,735 ZNF438
    nsv3909029copy number variation1nstd102humanBenign GRCh37 chr10: 31,247,142-31,275,977 , GRCh38.p12 chr10: 30,958,213-30,987,048 ZNF438
    nsv3895920copy number variation1nstd102humanBenign GRCh37 chr10: 31,247,387-31,275,977 , GRCh38.p12 chr10: 30,958,458-30,987,048 ZNF438
    nsv3901102copy number variation1nstd102humanBenign GRCh37 chr10: 31,154,799-31,328,360 , GRCh38.p12 chr10: 30,865,870-31,039,431 ZNF438, DDX10P1, 1 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 ZNF438, RNU7-12P, 1876 more genes
    nsv6290264copy number variation1nstd102humanPathogenic GRCh37 chr10: 30,624,523-33,688,350 , GRCh38.p12 chr10: 30,335,594-33,399,422 ZNF438, PPIAP31, 54 more genes
    nsv3906389copy number variation1nstd102humanPathogenic GRCh37 chr10: 73,232-135,524,321 , GRCh38.p12 chr10: 27,296-133,786,996 ZNF438, LOC100419870, 2105 more genes
    nsv3891157copy number variation1nstd102humanPathogenic GRCh37 chr10: 98,087-135,477,883 , GRCh38.p12 chr10: 52,147-133,740,558 ZNF438, AGAP14P, 2097 more genes
    nsv3902271copy number variation2nstd102humanPathogenic GRCh37 chr10: 100,027-135,427,143 , GRCh38.p12 chr10: 54,087-133,613,639 ZNF438, ANXA11, 2085 more genes
    nsv3891958copy number variation1nstd102humanPathogenic GRCh37 chr10: 93,297-135,378,918 , GRCh38.p12 chr10: 47,357-133,565,414 ZNF438, TUBB8, 2085 more genes
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 ZNF438, EXOC6, 1906 more genes
    nsv3904390copy number variation1nstd102humanPathogenic GRCh37 chr10: 100,026-50,961,640 , GRCh38.p12 chr10: 54,086-49,753,594 ZNF438, LINC00700, 806 more genes
    nsv3920796copy number variation1nstd102humanPathogenic NCBI36 chr10: 62,842-35,729,127 , GRCh37.p13 chr10: 72,842-35,689,121 , GRCh38.p12 chr10: 26,906-35,400,193 ZNF438, EPC1-AS1, 559 more genes
    nsv6313952copy number variation1nstd102humanPathogenic GRCh37 chr10: 6,273,934-34,732,521 , GRCh38.p12 chr10: 6,231,971-34,443,593 ZNF438, RPL36AP55, 418 more genes
    nsv3911634copy number variation1nstd102humanLikely pathogenic NCBI36 chr10: 19,417,096-33,061,227 , GRCh37 chr10: 19,377,090-33,021,221 , GRCh38 chr10: 19,088,161-32,732,293 ZNF438, BMI1, 221 more genes
    nsv3920598copy number variation1nstd102humanBenign NCBI36 chr10: 4,636,926-47,125,152 , GRCh38 chr10: 4,604,734-48,074,662 , GRCh37 chr10: 4,646,926-47,531,169 ZNF438, LOC100420467, 709 more genes
    nsv6290893copy number variation1nstd102humannot provided GRCh37 chr10: 135,655-47,688,677 , GRCh38.p12 chr10: 89,715-47,923,579 ZNF438, C1QL3, 774 more genes
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