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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4975399copy number variation1nstd200human GRCh38 chr10: 23,345,060-23,345,191 , GRCh37.p13 chr10: 23,633,989-23,634,120 C10orf67, C10orf67-AS1
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 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
    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
    nsv3911634copy number variation1nstd102humanLikely pathogenic NCBI36 chr10: 19,417,096-33,061,227 , GRCh37 chr10: 19,377,090-33,021,221 , GRCh38 chr10: 19,088,161-32,732,293 BMI1, CCND3P1, 221 more genes
    nsv3907985copy number variation1nstd102humanBenign GRCh37 chr10: 23,624,156-23,635,612 , GRCh38.p12 chr10: 23,335,227-23,346,683 C10orf67, C10orf67-AS1
    nsv3906389copy number variation1nstd102humanPathogenic GRCh37 chr10: 73,232-135,524,321 , GRCh38.p12 chr10: 27,296-133,786,996 LOC100419870, LOC102724439, 2105 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
    nsv3902340copy number variation1nstd102humanBenign GRCh37 chr10: 23,580,058-23,635,874 , GRCh38.p12 chr10: 23,291,129-23,346,945 C10orf67-AS1, C10orf67
    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
    nsv3891157copy number variation1nstd102humanPathogenic GRCh37 chr10: 98,087-135,477,883 , GRCh38.p12 chr10: 52,147-133,740,558 AGAP14P, LOC100505502, 2097 more genes
    nsv3238656insertion9nstd152human GRCh38 chr10: 23,330,520-23,344,569 , GRCh37.p13 chr10: 23,619,449-23,633,498 C10orf67, C10orf67-AS1
    nsv3169255copy number variation1nstd158human GRCh37 chr10: 6,588,549-24,063,075 , GRCh38.p12 chr10: 6,546,587-23,774,146 , ATP5F1C, 247 more genes
    nsv3168485inversion1nstd158human GRCh37 chr10: 8,177,319-27,193,925 , GRCh38.p12 chr10: 8,135,356-26,904,996 , BMI1, 257 more genes
    nsv1510579short tandem repeat10nstd128human GRCh37 chr10: 23,631,148-23,631,180 , GRCh38.p12 chr10: 23,342,219-23,342,251 C10orf67-AS1, C10orf67
    nsv1510578short tandem repeat3nstd128human GRCh37 chr10: 23,631,096-23,631,119 , GRCh38.p12 chr10: 23,342,167-23,342,190 C10orf67-AS1, C10orf67
    nsv1510163short tandem repeat1nstd128human GRCh37 chr10: 23,634,112-23,634,131 , GRCh38.p12 chr10: 23,345,183-23,345,202 C10orf67-AS1, C10orf67
    nsv1360236copy number variation5nstd122human NCBI36 chr10: 23,673,572-23,675,827 , GRCh37.p13 chr10: 23,633,566-23,635,821 , GRCh38.p12 chr10: 23,344,637-23,346,892 C10orf67, C10orf67-AS1
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