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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv3906389copy number variation1nstd102humanPathogenic GRCh37 chr10: 73,232-135,524,321 , GRCh38.p12 chr10: 27,296-133,786,996 LOC100419870, LOC102724439, 2105 more genes
    nsv3891157copy number variation1nstd102humanPathogenic GRCh37 chr10: 98,087-135,477,883 , GRCh38.p12 chr10: 52,147-133,740,558 AGAP14P, LOC100505502, 2097 more genes
    nsv3902271copy number variation2nstd102humanPathogenic GRCh37 chr10: 100,027-135,427,143 , GRCh38.p12 chr10: 54,087-133,613,639 ANXA11, EDRF1-DT, 2085 more genes
    nsv3891958copy number variation1nstd102humanPathogenic GRCh37 chr10: 93,297-135,378,918 , GRCh38.p12 chr10: 47,357-133,565,414 TUBB8, PPP2R2D, 2085 more genes
    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
    nsv3904390copy number variation1nstd102humanPathogenic GRCh37 chr10: 100,026-50,961,640 , GRCh38.p12 chr10: 54,086-49,753,594 LINC00700, LINC02881, 806 more genes
    nsv3917047copy number variation1nstd102humanPathogenic NCBI36 chr10: 42,500,760-75,145,672 , GRCh37 chr10: 43,180,754-75,475,666 , GRCh38 chr10: 42,685,306-73,715,908 SLC9A3P3, JMJD1C-AS2, 476 more genes
    nsv3921181copy number variation1nstd102humanPathogenic NCBI36 chr10: 41,927,641-68,830,439 , GRCh38 chr10: 42,112,187-67,400,675 , GRCh37 chr10: 42,607,635-69,160,433 AGAP6, A1CF, 338 more genes
    nsv3919301copy number variation1nstd102humanPathogenic NCBI36 chr10: 43,277,502-55,351,191 , GRCh37.p13 chr10: 43,957,496-55,681,185 , GRCh38.p12 chr10: 38,980,309-49,959,916 FAM245B, NPY4R2, 196 more genes
    nsv3916253copy number variation1nstd102humanPathogenic GRCh38 chr10: 42,884,294-52,265,317 , NCBI36 chr10: 42,699,748-53,695,083 , GRCh37 chr10: 43,379,742-54,025,077 PTPN20CP, ASAH2, 198 more genes
    nsv3918611copy number variation1nstd102humanPathogenic GRCh38 chr10: 42,395,201-50,877,059 , NCBI36 chr10: 42,210,655-52,306,825 , GRCh37 chr10: 42,890,649-52,636,819 LOC105378289, FAM170B-AS1, 211 more genes
    nsv3972353copy number variation1nstd102humanLikely pathogenic GRCh37 chr10: 37,149,872-46,169,876 , GRCh38.p12 chr10: 36,860,944-45,674,428 ALOX5, HNRNPF, 132 more genes
    nsv3923539inversion1nstd102humanLikely pathogenic GRCh38.p12 chr10: 43,115,743-59,903,521 , GRCh37 chr10: 43,611,191-61,663,279 ALOX5, CHAT, 248 more genes
    nsv3896990copy number variation1nstd102humanLikely benign GRCh37 chr10: 45,997,573-46,293,591 , GRCh38.p12 chr10: 45,502,125-45,798,143 ZFAND4, MARCHF8, 5 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
    nsv3899904copy number variation1nstd102humanBenign GRCh37 chr10: 46,052,917-47,940,417 , GRCh38.p12 chr10: 45,557,469-47,923,579 RN7SL248P, FAM25BP, 70 more genes
    nsv3890908copy number variation1nstd102humanBenign GRCh37 chr10: 46,083,500-47,940,417 , GRCh38.p12 chr10: 45,588,052-47,923,579 SYT15, AHCYP1, 70 more genes
    nsv3909635copy number variation1nstd102humanBenign GRCh37 chr10: 46,109,533-47,662,831 , GRCh38.p12 chr10: 45,614,085-47,923,579 LOC105378291, FAM21FP, 69 more genes
    nsv3909506copy number variation1nstd102humanBenign GRCh37 chr10: 46,109,533-47,695,269 , GRCh38.p12 chr10: 45,614,085-47,923,579 FAM25BP, LOC105378287, 69 more genes
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