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    Number of Variants: 10

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112755copy number variation1nstd102humanPathogenic GRCh37 chr12: 65,251,705-75,263,379 , GRCh38.p12 chr12: 64,857,925-74,869,599 SLC35E3, LINC02421, 144 more genes
    nsv7093395copy number variation1nstd102humanPathogenic GRCh37 chr12: 64,609,458-70,352,103 , GRCh38.p12 chr12: 64,215,678-69,958,323 SLC35E3, TODL, 116 more genes
    nsv3911433copy number variation1nstd102humanPathogenic NCBI36 chr12: 64,125,223-69,706,384 , GRCh38 chr12: 65,445,176-71,026,337 , GRCh37 chr12: 65,838,956-71,420,117 SLC35E3, CCT2, 100 more genes
    nsv4729265copy number variation1nstd102humanPathogenic GRCh37 chr12: 68,572,386-70,833,868 , GRCh38.p12 chr12: 68,178,606-70,440,088 SLC35E3, LINC02384, 47 more genes
    nsv3904242copy number variation1nstd102humanPathogenic GRCh37 chr12: 1-133,851,895 , GRCh38.p12 chr12: 45,740-133,265,309 SLC35E3, RNA5SP369, 2454 more genes
    nsv3905447copy number variation2nstd102humanPathogenic GRCh37 chr12: 173,787-133,777,902 , GRCh38.p12 chr12: 64,621-133,201,316 SLC35E3, LOH12CR2, 2452 more genes
    nsv3897722copy number variation1nstd102humanPathogenic GRCh37 chr12: 191,619-133,777,645 , GRCh38.p12 chr12: 82,453-133,201,059 SLC35E3, RNU4ATAC16P, 2452 more genes
    nsv3914194copy number variation1nstd102humanPathogenic NCBI36 chr12: 100,698-132,283,466 , GRCh37 chr12: 282,465-133,773,393 , GRCh38 chr12: 121,271-133,196,807 SLC35E3, BTG1P1, 2451 more genes
    nsv3904719copy number variation1nstd102humanPathogenic GRCh37 chr12: 621,220-133,779,118 , GRCh38.p12 chr12: 512,054-133,202,532 SLC35E3, OR5BT1P, 2441 more genes
    nsv3918556copy number variation1nstd102humanLikely pathogenic NCBI36 chr12: 66,691,464-74,063,101 , GRCh37 chr12: 68,405,197-75,776,834 , GRCh38 chr12: 68,011,417-75,383,054 SLC35E3, CPM, 97 more genes
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