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Items: 1 to 20 of 162

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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
    nsv7074105inversion1nstd229human GRCh38 chr10: 17,945,641-22,801,235 , GRCh37.p13 chr10: 18,252,931-23,090,164 UBE2V2P1, LOC105376450, 62 more genes
    nsv7063218inversion1nstd229human GRCh38 chr10: 21,664,813-22,447,089 , GRCh37.p13 chr10: 21,953,742-22,736,018 PSME2P6, LOC107984214, 16 more genes
    nsv6883501copy number variation1nstd229human GRCh38 chr10: 22,316,014-22,316,052 , GRCh37.p13 chr10: 22,604,943-22,604,981 COMMD3-BMI1, COMMD3
    nsv6878415copy number variation1nstd229human GRCh38 chr10: 22,309,501-22,317,700 , GRCh37.p13 chr10: 22,598,430-22,606,629 COMMD3, COMMD3-BMI1
    nsv6638019copy number variation1nstd102humanUncertain significance GRCh37 chr10: 22,208,767-23,220,277 , GRCh38.p12 chr10: 21,919,838-22,931,348 ADIPOR1P1, LINC03027, 19 more genes
    nsv6449826copy number variation1nstd223human GRCh38 chr10: 22,312,201-22,359,700 , GRCh37.p13 chr10: 22,601,130-22,648,629 COMMD3-BMI1, COMMD3, 2 more genes
    nsv6446055copy number variation1nstd223human GRCh38 chr10: 22,309,901-22,362,700 , GRCh37.p13 chr10: 22,598,830-22,651,629 BMI1, COMMD3-BMI1, 2 more genes
    nsv6443590copy number variation1nstd223human GRCh38 chr10: 22,316,801-22,320,200 , GRCh37.p13 chr10: 22,605,730-22,609,129 COMMD3-BMI1, COMMD3, 1 more genes
    nsv6440531copy number variation1nstd223human GRCh38 chr10: 22,232,001-22,375,900 , GRCh37.p13 chr10: 22,520,930-22,664,829 BMI1, RPL31P45, 5 more genes
    nsv6438696copy number variation1nstd223human GRCh38 chr10: 22,311,201-22,320,400 , GRCh37.p13 chr10: 22,600,130-22,609,329 COMMD3, COMMD3-BMI1, 1 more genes
    nsv6313952copy number variation1nstd102humanPathogenic GRCh37 chr10: 6,273,934-34,732,521 , GRCh38.p12 chr10: 6,231,971-34,443,593 RPL36AP55, HNRNPA1P32, 418 more genes
    nsv6302250copy number variation1nstd186human GRCh37 chr10: 22,605,868-22,606,530 , GRCh38.p12 chr10: 22,316,939-22,317,601 COMMD3-BMI1, COMMD3
    nsv6290893copy number variation1nstd102humannot provided GRCh37 chr10: 135,655-47,688,677 , GRCh38.p12 chr10: 89,715-47,923,579 C1QL3, LOC105376441, 774 more genes
    nsv6132032copy number variation1nstd213human GRCh37 chr10: 21,540,000-22,750,001 , GRCh38.p12 chr10: 21,251,071-22,461,072 BMI1, MLLT10, 29 more genes
    nsv6132031copy number variation1nstd213human GRCh37 chr10: 18,100,000-28,260,001 , GRCh38.p12 chr10: 17,839,748-27,971,072 BMI1, CACNB2, 136 more genes
    nsv5484935copy number variation1nstd206human GRCh38 chr10: 22,316,939-22,317,601 , GRCh37.p13 chr10: 22,605,868-22,606,530 COMMD3, COMMD3-BMI1
    nsv4613862copy number variation1nstd183human GRCh37 chr10: 22,605,225-22,610,822 , GRCh38.p12 chr10: 22,316,296-22,321,893 COMMD3, COMMD3-BMI1, 1 more genes
    nsv4610390copy number variation1nstd183human GRCh37 chr10: 22,609,162-22,617,484 , GRCh38.p12 chr10: 22,320,233-22,328,555 BMI1, COMMD3-BMI1, 1 more genes
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