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Items: 1 to 20 of 29

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3905655copy number variation1nstd102humanBenign GRCh37 chr10: 22,603,581-22,639,707 , GRCh38.p12 chr10: 22,314,652-22,350,778 BMI1, SPAG6, 2 more genes
    nsv3907360copy number variation1nstd102humanBenign GRCh37 chr10: 22,597,174-22,679,177 , GRCh38.p12 chr10: 22,308,245-22,390,248 BMI1, COMMD3-BMI1, 2 more genes
    nsv3890692copy number variation1nstd102humanBenign GRCh37 chr10: 22,601,976-22,675,857 , GRCh38.p12 chr10: 22,313,047-22,386,928 BMI1, COMMD3, 2 more genes
    nsv3908588copy number variation1nstd102humanBenign GRCh37 chr10: 22,594,765-22,639,707 , GRCh38.p12 chr10: 22,305,836-22,350,778 BMI1, SPAG6, 2 more genes
    nsv3906141copy number variation1nstd102humanBenign GRCh37 chr10: 22,594,765-22,637,381 , GRCh38.p12 chr10: 22,305,836-22,348,452 BMI1, COMMD3, 2 more genes
    nsv3907107copy number variation1nstd102humanBenign GRCh37 chr10: 22,597,174-22,637,381 , GRCh38.p12 chr10: 22,308,245-22,348,452 BMI1, COMMD3, 2 more genes
    nsv3908299copy number variation1nstd102humanBenign GRCh37 chr10: 22,601,976-22,639,707 , GRCh38.p12 chr10: 22,313,047-22,350,778 BMI1, COMMD3, 2 more genes
    nsv3895110copy number variation1nstd102humanBenign GRCh37 chr10: 22,601,976-22,637,381 , GRCh38.p12 chr10: 22,313,047-22,348,452 BMI1, COMMD3, 2 more genes
    nsv3904392copy number variation1nstd102humanBenign GRCh37 chr10: 22,603,581-22,637,381 , GRCh38.p12 chr10: 22,314,652-22,348,452 BMI1, COMMD3, 2 more genes
    nsv3899582copy number variation1nstd102humanBenign GRCh37 chr10: 22,607,432-22,637,381 , GRCh38.p12 chr10: 22,318,503-22,348,452 BMI1, COMMD3-BMI1, 2 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 BMI1, RNU7-12P, 1876 more genes
    nsv3906389copy number variation1nstd102humanPathogenic GRCh37 chr10: 73,232-135,524,321 , GRCh38.p12 chr10: 27,296-133,786,996 BMI1, LOC100419870, 2105 more genes
    nsv3891157copy number variation1nstd102humanPathogenic GRCh37 chr10: 98,087-135,477,883 , GRCh38.p12 chr10: 52,147-133,740,558 BMI1, AGAP14P, 2097 more genes
    nsv3902271copy number variation2nstd102humanPathogenic GRCh37 chr10: 100,027-135,427,143 , GRCh38.p12 chr10: 54,087-133,613,639 BMI1, ANXA11, 2085 more genes
    nsv3891958copy number variation1nstd102humanPathogenic GRCh37 chr10: 93,297-135,378,918 , GRCh38.p12 chr10: 47,357-133,565,414 BMI1, TUBB8, 2085 more genes
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 BMI1, EXOC6, 1906 more genes
    nsv3904390copy number variation1nstd102humanPathogenic GRCh37 chr10: 100,026-50,961,640 , GRCh38.p12 chr10: 54,086-49,753,594 BMI1, 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 BMI1, 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 BMI1, RPL36AP55, 418 more genes
    nsv3917667copy number variation1nstd102humanPathogenic GRCh37 chr10: 224,406-26,628,907 , GRCh38 chr10: 90,205-26,339,978 , NCBI36 chr10: 126,145-26,668,913 BMI1, RN7SKP241, 389 more genes
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