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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3894437copy number variation1nstd102humanUncertain significance GRCh37 chr10: 51,910,584-52,128,786 , GRCh38.p12 chr10: 50,150,824-50,369,026 ASAH2, DYNC1I2P1, 2 more genes
    nsv3893952copy number variation1nstd102humanUncertain significance GRCh37 chr10: 51,974,581-52,155,084 , GRCh38.p12 chr10: 50,214,821-50,395,324 ASAH2, DYNC1I2P1, 1 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 ASAH2, RNU7-12P, 1876 more genes
    nsv4675455copy number variation1nstd102humanPathogenic GRCh37 chr10: 50,250,603-69,256,083 , GRCh38.p12 chr10: 45,931,517-67,496,325 ASAH2, MRLN, 242 more genes
    nsv3919674copy number variation1nstd102humanPathogenic NCBI36 chr10: 49,100,986-52,085,077 , GRCh38 chr10: 45,931,517-50,655,311 , GRCh37 chr10: 49,430,980-52,415,071 ASAH2, AGAP12P, 111 more genes
    nsv3906389copy number variation1nstd102humanPathogenic GRCh37 chr10: 73,232-135,524,321 , GRCh38.p12 chr10: 27,296-133,786,996 ASAH2, LOC100419870, 2105 more genes
    nsv3891157copy number variation1nstd102humanPathogenic GRCh37 chr10: 98,087-135,477,883 , GRCh38.p12 chr10: 52,147-133,740,558 ASAH2, AGAP14P, 2097 more genes
    nsv3902271copy number variation2nstd102humanPathogenic GRCh37 chr10: 100,027-135,427,143 , GRCh38.p12 chr10: 54,087-133,613,639 ASAH2, ANXA11, 2085 more genes
    nsv3891958copy number variation1nstd102humanPathogenic GRCh37 chr10: 93,297-135,378,918 , GRCh38.p12 chr10: 47,357-133,565,414 ASAH2, TUBB8, 2085 more genes
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 ASAH2, EXOC6, 1906 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 ASAH2, SLC9A3P3, 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 ASAH2, AGAP6, 338 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 ASAH2, PTPN20CP, 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 ASAH2, LOC105378289, 211 more genes
    nsv3972371copy number variation1nstd102humanLikely pathogenic GRCh37 chr10: 49,390,457-60,061,643 , GRCh38.p12 chr10: 45,931,517-58,301,883 ASAH2, CHAT, 156 more genes
    nsv3923539inversion1nstd102humanLikely pathogenic GRCh38.p12 chr10: 43,115,743-59,903,521 , GRCh37 chr10: 43,611,191-61,663,279 ASAH2, ALOX5, 248 more genes
    nsv4729053copy number variation1nstd102humanLikely benign GRCh37 chr10: 51,753,154-52,166,339 , GRCh38.p12 chr10: 49,993,394-50,406,579 ASAH2, SLC9A3P3, 7 more genes
    nsv3890793copy number variation1nstd102humanLikely benign GRCh37 chr10: 51,790,819-52,167,537 , GRCh38.p12 chr10: 50,031,059-50,407,777 ASAH2, SLC9A3P1, 4 more genes
    nsv3907664copy number variation1nstd102humandrug response GRCh37 chr10: 42,347,406-135,534,747 , GRCh38.p12 chr10: 42,101,241-133,787,422 ASAH2, SHOC2, 1487 more genes
    nsv4675379copy number variation1nstd102humanUncertain significance GRCh37 chr10: 51,659,413-52,476,136 , GRCh38.p12 chr10: 49,959,917-50,716,376 ASAH2, TIMM23B-AGAP6, 18 more genes
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