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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4675448copy number variation1nstd102humanUncertain significance GRCh37 chr10: 12,073,932-12,165,984 , GRCh38.p12 chr10: 12,031,933-12,123,985 UPF2, RNU6-88P, 2 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 UPF2, COX6CP17, 302 more genes
    nsv3884983copy number variation1nstd102humanPathogenic GRCh37 chr10: 4,689,760-19,120,882 , GRCh38.p12 chr10: 4,647,568-18,831,953 UPF2, HSPA14, 228 more genes
    nsv3911783copy number variation1nstd102humanPathogenic NCBI36 chr10: 7,510,738-21,916,687 , GRCh37 chr10: 7,470,732-21,876,681 , GRCh38 chr10: 7,428,770-21,587,752 UPF2, LOC101928834, 192 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 UPF2, IL9RP2, 232 more genes
    nsv3890577copy number variation1nstd102humanPathogenic GRCh37 chr10: 100,026-12,842,179 , GRCh38.p12 chr10: 54,086-12,800,180 UPF2, 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 UPF2, LINC02656, 200 more genes
    nsv5381768copy number variation1nstd102humanPathogenic GRCh37 chr10: 9,137,489-17,227,168 , GRCh38.p12 chr10: 9,095,526-17,185,169 UPF2, PROSER2, 110 more genes
    nsv3906389copy number variation1nstd102humanPathogenic GRCh37 chr10: 73,232-135,524,321 , GRCh38.p12 chr10: 27,296-133,786,996 UPF2, LOC100419870, 2105 more genes
    nsv3891157copy number variation1nstd102humanPathogenic GRCh37 chr10: 98,087-135,477,883 , GRCh38.p12 chr10: 52,147-133,740,558 UPF2, AGAP14P, 2097 more genes
    nsv3902271copy number variation2nstd102humanPathogenic GRCh37 chr10: 100,027-135,427,143 , GRCh38.p12 chr10: 54,087-133,613,639 UPF2, ANXA11, 2085 more genes
    nsv3891958copy number variation1nstd102humanPathogenic GRCh37 chr10: 93,297-135,378,918 , GRCh38.p12 chr10: 47,357-133,565,414 UPF2, TUBB8, 2085 more genes
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 UPF2, EXOC6, 1906 more genes
    nsv3904390copy number variation1nstd102humanPathogenic GRCh37 chr10: 100,026-50,961,640 , GRCh38.p12 chr10: 54,086-49,753,594 UPF2, 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 UPF2, 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 UPF2, 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 UPF2, RN7SKP241, 389 more genes
    nsv3924406copy number variation1nstd102humanPathogenic GRCh38 chr10: 69,261-19,184,047 , GRCh37 chr10: 224,406-19,472,976 , NCBI36 chr10: 105,201-19,512,982 UPF2, WDR37, 302 more genes
    nsv3920285copy number variation1nstd102humanPathogenic NCBI36 chr10: 106,418-15,455,341 , GRCh37.p13 chr10: 116,418-15,415,335 , GRCh38.p12 chr10: 70,478-15,373,336 UPF2, NRBF2P5, 265 more genes
    nsv4455607copy number variation2nstd102humanPathogenic GRCh37 chr10: 100,026-15,273,144 , GRCh38.p12 chr10: 54,086-15,231,145 UPF2, LOC105376357, 264 more genes
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