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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3901812copy number variation1nstd102humanBenign GRCh37 chr10: 5,063,398-5,121,745 , GRCh38.p12 chr10: 5,021,206-5,079,553 AKR1C3, LOC107984198
    nsv3905870copy number variation1nstd102humanBenign GRCh37 chr10: 5,084,728-5,136,651 , GRCh38.p12 chr10: 5,042,536-5,094,459 AKR1C3, LOC107984198
    nsv3894198copy number variation1nstd102humanBenign GRCh37 chr10: 5,018,712-5,144,037 , GRCh38.p12 chr10: 4,976,520-5,101,845 AKR1C3, AKR1C2, 3 more genes
    nsv4456669copy number variation1nstd102humanUncertain significance GRCh37 chr10: 5,056,553-5,174,423 , GRCh38.p12 chr10: 5,014,361-5,132,231 AKR1C3, AKR1C2, 1 more genes
    nsv3914771copy number variation1nstd102humanPathogenic GRCh38 chr10: 54,086-19,336,980 , NCBI36 chr10: 90,026-19,665,915 , GRCh37 chr10: 100,026-19,625,909 AKR1C3, COX6CP17, 302 more genes
    nsv3884983copy number variation1nstd102humanPathogenic GRCh37 chr10: 4,689,760-19,120,882 , GRCh38.p12 chr10: 4,647,568-18,831,953 AKR1C3, HSPA14, 228 more genes
    nsv3918372copy number variation1nstd102humanPathogenic GRCh38 chr10: 70,478-13,736,564 , GRCh37 chr10: 224,406-13,778,564 , NCBI36 chr10: 106,418-13,818,570 AKR1C3, IL9RP2, 232 more genes
    nsv3890577copy number variation1nstd102humanPathogenic GRCh37 chr10: 100,026-12,842,179 , GRCh38.p12 chr10: 54,086-12,800,180 AKR1C3, LOC105376364, 208 more genes
    nsv3911206copy number variation1nstd102humanPathogenic GRCh37 chr10: 4,844,945-16,865,490 , NCBI36 chr10: 4,834,945-16,905,496 , GRCh38 chr10: 4,802,753-16,823,491 AKR1C3, LINC02656, 200 more genes
    nsv3893746copy number variation1nstd102humanPathogenic GRCh37 chr10: 136,361-8,850,609 , GRCh38.p12 chr10: 90,421-8,808,646 AKR1C3, TRV-TAC3-1, 163 more genes
    nsv5672604copy number variation1nstd102humanPathogenic GRCh37 chr10: 120,001-6,920,000 , GRCh38.p12 chr10: 74,061-6,878,038 AKR1C3, PITRM1-AS1, 133 more genes
    nsv3924022copy number variation1nstd102humanPathogenic NCBI36 chr10: 105,200-6,291,337 , GRCh38 chr10: 69,260-6,209,368 , GRCh37 chr10: 224,406-6,251,331 AKR1C3, LINC02561, 120 more genes
    nsv3907813copy number variation1nstd102humanPathogenic GRCh37 chr10: 2,593,113-8,484,746 , GRCh38.p12 chr10: 2,550,921-8,442,783 AKR1C3, AKR1C6P, 121 more genes
    nsv3917165copy number variation1nstd102humanPathogenic NCBI36 chr10: 62,842-5,292,166 , GRCh37.p13 chr10: 72,842-5,302,166 , GRCh38.p12 chr10: 26,906-5,260,203 AKR1C3, LINC02668, 85 more genes
    nsv6290250copy number variation1nstd102humanPathogenic GRCh37 chr10: 60,501-5,238,964 , GRCh38.p12 chr10: 14,561-5,197,001 AKR1C3, TUBB8, 85 more genes
    nsv3906389copy number variation1nstd102humanPathogenic GRCh37 chr10: 73,232-135,524,321 , GRCh38.p12 chr10: 27,296-133,786,996 AKR1C3, LOC100419870, 2105 more genes
    nsv3891157copy number variation1nstd102humanPathogenic GRCh37 chr10: 98,087-135,477,883 , GRCh38.p12 chr10: 52,147-133,740,558 AKR1C3, AGAP14P, 2097 more genes
    nsv3902271copy number variation2nstd102humanPathogenic GRCh37 chr10: 100,027-135,427,143 , GRCh38.p12 chr10: 54,087-133,613,639 AKR1C3, ANXA11, 2085 more genes
    nsv3891958copy number variation1nstd102humanPathogenic GRCh37 chr10: 93,297-135,378,918 , GRCh38.p12 chr10: 47,357-133,565,414 AKR1C3, TUBB8, 2085 more genes
    nsv3904390copy number variation1nstd102humanPathogenic GRCh37 chr10: 100,026-50,961,640 , GRCh38.p12 chr10: 54,086-49,753,594 AKR1C3, LINC00700, 806 more genes
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