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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5347576translocation1nstd200human GRCh38 chr10: 22,210,721-22,210,721 , GRCh38 chr10: 22,209,633-22,209,633 , GRCh37.p13 chr10: 22,499,650-22,499,650 , GRCh37.p13 chr10: 22,498,562-22,498,562 EBLN1
    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
    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
    nsv3903440copy number variation1nstd102humanUncertain significance GRCh37 chr10: 21,881,989-23,129,991 , GRCh38.p12 chr10: 21,593,060-22,841,062 TRN-GTT2-3, DNAJC1, 22 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
    nsv3891157copy number variation1nstd102humanPathogenic GRCh37 chr10: 98,087-135,477,883 , GRCh38.p12 chr10: 52,147-133,740,558 AGAP14P, LOC100505502, 2097 more genes
    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
    nsv1398579copy number variation1nstd102humanUncertain significance GRCh37 chr10: 22,193,496-22,634,700 , GRCh38.p12 chr10: 21,904,567-22,345,771 DNAJC1, TRN-GTT2-3, 11 more genes
    nsv1190813copy number variation1nstd113human NCBI36 chr10: 19,013,124-22,708,266 , GRCh37.p13 chr10: 18,973,118-22,668,260 , GRCh38.p12 chr10: 18,684,189-22,379,331 BMI1, SKIDA1, 50 more genes
    esv3806028tandem duplication1estd192human GRCh37 chr10: 4,904,244-93,524,835 , GRCh38.p12 chr10: 4,862,052-91,765,078 , ARHGAP12, 1364 more genes
    esv3807612copy number variation1estd192human GRCh37 chr10: 18,765,925-32,438,606 , GRCh38.p12 chr10: 18,476,996-32,149,678 , WAC-AS1, 223 more genes
    esv3801105insertion1estd192human GRCh38.p12 chr10: 21,999,087-86,031,971 , GRCh37 chr10: 22,288,016-87,791,728 , ADK, 972 more genes
    esv3802920copy number variation1estd192human GRCh37 chr10: 191,341-29,497,594 , GRCh38.p12 chr10: 145,401-29,208,665 , LOC102724245, 469 more genes
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