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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5942272copy number variation1nstd209human GRCh38 chr12: 81,120,340-81,126,064 , GRCh37.p13 chr12: 81,514,119-81,519,843 LOC107984535, ACSS3
    nsv5940546copy number variation1nstd209human GRCh38 chr12: 81,097,871-81,100,952 , GRCh37.p13 chr12: 81,491,650-81,494,731 ACSS3, LOC107984535
    nsv5938456copy number variation1nstd209human GRCh38 chr12: 81,158,222-81,159,507 , GRCh37.p13 chr12: 81,552,001-81,553,286 ACSS3, MIR4699
    nsv5936678copy number variation1nstd209human GRCh38 chr12: 81,111,627-81,112,753 , GRCh37.p13 chr12: 81,505,406-81,506,532 ACSS3, LOC107984535
    nsv5866779copy number variation1nstd209human GRCh38 chr12: 81,090,431-81,092,458 , GRCh37.p13 chr12: 81,484,210-81,486,237 ACSS3, LOC107984535
    nsv5860586copy number variation1nstd209human GRCh38 chr12: 81,158,475-81,159,574 , GRCh37.p13 chr12: 81,552,254-81,553,353 MIR4699, ACSS3
    nsv5858962copy number variation1nstd209human GRCh38 chr12: 81,097,854-81,100,982 , GRCh37.p13 chr12: 81,491,633-81,494,761 LOC107984535, ACSS3
    nsv5856391copy number variation1nstd209human GRCh38 chr12: 81,120,238-81,126,097 , GRCh37.p13 chr12: 81,514,017-81,519,876 ACSS3, LOC107984535
    nsv5853285copy number variation2nstd209human GRCh38 chr12: 81,111,538-81,113,037 , GRCh37.p13 chr12: 81,505,317-81,506,816 LOC107984535, ACSS3
    nsv5848654copy number variation2nstd209human GRCh38 chr12: 81,098,283-81,101,427 , GRCh37.p13 chr12: 81,492,062-81,495,206 ACSS3, LOC107984535
    nsv5727871mobile element insertion1nstd211human GRCh38 chr12: 81,083,319-81,083,319 , GRCh37.p13 chr12: 81,477,098-81,477,098 ACSS3
    nsv5708962mobile element insertion2nstd211human GRCh38 chr12: 81,120,790-81,120,790 , GRCh37.p13 chr12: 81,514,569-81,514,569 ACSS3, LOC107984535
    nsv5697593mobile element insertion1nstd211human GRCh38 chr12: 81,208,718-81,208,718 , GRCh37.p13 chr12: 81,602,497-81,602,497 ACSS3
    nsv5659429insertion1nstd207human GRCh38 chr12: 81,213,840-81,213,840 , GRCh37.p13 chr12: 81,607,619-81,607,619 ACSS3
    nsv5558725mobile element insertion1nstd206human GRCh38 chr12: 81,083,319-81,083,370 , GRCh37.p13 chr12: 81,477,098-81,477,149 ACSS3
    nsv5512076copy number variation1nstd206human GRCh38 chr12: 81,120,342-81,126,065 , GRCh37.p13 chr12: 81,514,121-81,519,844 ACSS3, LOC107984535
    nsv5500934copy number variation1nstd206human GRCh38 chr12: 76,069,603-82,449,398 , GRCh37.p13 chr12: 76,463,383-82,843,177 , E2F7, 65 more genes
    nsv5500189copy number variation1nstd206human GRCh38 chr12: 81,118,720-81,118,796 , GRCh37.p13 chr12: 81,512,499-81,512,575 ACSS3, LOC107984535
    nsv5500164copy number variation1nstd206human GRCh38 chr12: 81,158,224-81,159,508 , GRCh37.p13 chr12: 81,552,003-81,553,287 ACSS3, MIR4699
    nsv5495851copy number variation1nstd206human GRCh38 chr12: 81,144,971-81,148,912 , GRCh37.p13 chr12: 81,538,750-81,542,691 ACSS3
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