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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098813copy number variation1nstd102humanPathogenic GRCh37 chr12: 176,047-34,179,852 , GRCh38.p12 chr12: 66,881-34,026,917 TDGP1, RPS4XP14, 680 more genes
    nsv7075508inversion1nstd229human GRCh38 chr12: 16,982,134-16,988,571 , GRCh37.p13 chr12: 17,135,068-17,141,505 LOC105369677, SKP1P2
    nsv7072996inversion1nstd229human GRCh38 chr12: 16,788,218-16,795,364 , GRCh37.p13 chr12: 16,941,152-16,948,298 LOC105369677
    nsv7068562inversion1nstd229human GRCh38 chr12: 16,889,384-16,892,290 , GRCh37.p13 chr12: 17,042,318-17,045,224 LOC105369677
    nsv7064011inversion1nstd229human GRCh38 chr12: 11,255,910-17,864,916 , GRCh37.p13 chr12: 11,408,826-18,017,850 MGP, MIR3974, 108 more genes
    nsv6937666copy number variation1nstd229human GRCh38 chr12: 16,729,413-16,899,744 , GRCh37.p13 chr12: 16,882,347-17,052,678 LOC105369677
    nsv6937013copy number variation1nstd229human GRCh38 chr12: 16,936,176-16,939,543 , GRCh37.p13 chr12: 17,089,110-17,092,477 LOC105369677
    nsv6936809copy number variation1nstd229human GRCh38 chr12: 16,987,546-16,991,484 , GRCh37.p13 chr12: 17,140,480-17,144,418 LOC105369677, EEF1A1P16, 1 more genes
    nsv6936477copy number variation1nstd229human GRCh38 chr12: 16,185,413-17,407,405 , GRCh37.p13 chr12: 16,338,347-17,560,339 RPL7P40, LOC105369677, 11 more genes
    nsv6936342copy number variation1nstd229human GRCh38 chr12: 16,987,201-17,019,100 , GRCh37.p13 chr12: 17,140,135-17,172,034 SKP1P2, EEF1A1P16, 1 more genes
    nsv6936057copy number variation1nstd229human GRCh38 chr12: 16,916,264-16,916,346 , GRCh37.p13 chr12: 17,069,198-17,069,280 LOC105369677
    nsv6935626copy number variation1nstd229human GRCh38 chr12: 16,926,232-16,956,105 , GRCh37.p13 chr12: 17,079,166-17,109,039 LOC105369677
    nsv6934616copy number variation1nstd229human GRCh38 chr12: 16,951,101-16,952,500 , GRCh37.p13 chr12: 17,104,035-17,105,434 LOC105369677
    nsv6932913copy number variation1nstd229human GRCh38 chr12: 16,960,522-16,986,245 , GRCh37.p13 chr12: 17,113,456-17,139,179 LOC105369677
    nsv6932694copy number variation1nstd229human GRCh38 chr12: 16,810,616-16,810,941 , GRCh37.p13 chr12: 16,963,550-16,963,875 LOC105369677
    nsv6932186copy number variation1nstd229human GRCh38 chr12: 16,759,462-16,870,792 , GRCh37.p13 chr12: 16,912,396-17,023,726 LOC105369677
    nsv6931775copy number variation1nstd229human GRCh38 chr12: 16,944,568-16,953,356 , GRCh37.p13 chr12: 17,097,502-17,106,290 LOC105369677
    nsv6931206copy number variation1nstd229human GRCh38 chr12: 16,982,163-16,984,093 , GRCh37.p13 chr12: 17,135,097-17,137,027 LOC105369677
    nsv6930981copy number variation1nstd229human GRCh38 chr12: 16,851,677-16,866,007 , GRCh37.p13 chr12: 17,004,611-17,018,941 LOC105369677
    nsv6930863copy number variation1nstd229human GRCh38 chr12: 16,840,101-16,840,245 , GRCh37.p13 chr12: 16,993,035-16,993,179 LOC105369677
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