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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5672604copy number variation1nstd102humanPathogenic GRCh37 chr10: 120,001-6,920,000 , GRCh38.p12 chr10: 74,061-6,878,038 PITRM1-AS1, TRV-TAC3-1, 133 more genes
    nsv4675507copy number variation1nstd102humanUncertain significance GRCh37 chr10: 5,201,443-5,658,539 , GRCh38.p12 chr10: 5,159,245-5,616,576 LASTR, LINC02561, 15 more genes
    nsv4609794copy number variation1nstd183human GRCh37 chr10: 5,411,034-5,447,218 , GRCh38.p12 chr10: 5,369,071-5,405,255 TUBAL3, UCN3
    nsv4603772copy number variation1nstd183human GRCh37 chr10: 5,416,127-5,446,753 , GRCh38.p12 chr10: 5,374,164-5,404,790 TUBAL3, UCN3
    nsv4455607copy number variation2nstd102humanPathogenic GRCh37 chr10: 100,026-15,273,144 , GRCh38.p12 chr10: 54,086-15,231,145 LOC105376357, LINC02649, 264 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 WDR37, LOC105376364, 302 more genes
    nsv3924330copy number variation1nstd102humanUncertain significance GRCh38 chr10: 4,605,831-7,403,265 , GRCh37 chr10: 4,648,023-7,445,227 , NCBI36 chr10: 4,638,023-7,485,233 AKR1C8, LINC02649, 67 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 LINC02561, AKR1C1, 120 more genes
    nsv3923991copy number variation1nstd102humanLikely pathogenic NCBI36 chr10: 1,633,367-9,285,698 , GRCh37 chr10: 1,643,367-9,245,692 , GRCh38 chr10: 1,601,172-9,203,729 ADARB2, ATP5F1C, 143 more genes
    nsv3923974copy number variation1nstd102humanPathogenic NCBI36 chr10: 109,796-12,897,920 , GRCh38 chr10: 73,856-12,815,915 , GRCh37 chr10: 119,796-12,857,914 LINC02663, LARP4B-DT, 208 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 EPC1-AS1, RNU6-452P, 559 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 LOC100420467, LOC105376474, 709 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 NRBF2P5, DDX20P1, 265 more genes
    nsv3919135copy number variation1nstd102humannot provided NCBI36 chr10: 1-6,889,456 , GRCh37.p13 chr10: 60,001-6,849,450 , GRCh38.p12 chr10: 14,062-6,807,488 ANKRD16, IL2RA, 133 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 IL9RP2, PRKCQ, 232 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 RN7SKP241, DIP2C-AS1, 389 more genes
    nsv3917516copy number variation1nstd102humanPathogenic GRCh37 chr10: 224,406-8,484,746 , NCBI36 chr10: 126,361-8,524,752 , GRCh38 chr10: 90,421-8,442,783 LINC02561, LOC107984199, 156 more genes
    nsv3917265copy number variation1nstd102humanUncertain significance GRCh38 chr10: 4,871,826-5,811,361 , GRCh37 chr10: 4,914,018-5,853,324 , NCBI36 chr10: 4,904,018-5,893,330 TUBAL3, LINC02561, 28 more genes
    nsv3915964copy number variation1nstd102humanPathogenic NCBI36 chr10: 90,026-13,287,922 , GRCh38 chr10: 54,086-13,205,916 , GRCh37 chr10: 100,026-13,247,916 LOC105376409, CELF2-DT, 217 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 COX6CP17, TUBAL3, 302 more genes
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