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Items: 9

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    Number of Variants: 9

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3924873copy number variation1nstd102humanPathogenic GRCh38 chr12: 53,224,024-54,222,450 , GRCh37 chr12: 53,617,808-54,616,234 , NCBI36 chr12: 51,904,075-52,902,501 HOXC6, PFDN5, 51 more genes
    nsv4436658copy number variation1nstd102humanPathogenic GRCh37 chr12: 53,784,698-54,741,363 , GRCh38.p12 chr12: 53,390,914-54,347,579 HOXC6, CALCOCO1, 53 more genes
    nsv3904242copy number variation1nstd102humanPathogenic GRCh37 chr12: 1-133,851,895 , GRCh38.p12 chr12: 45,740-133,265,309 HOXC6, RNA5SP369, 2454 more genes
    nsv3905447copy number variation2nstd102humanPathogenic GRCh37 chr12: 173,787-133,777,902 , GRCh38.p12 chr12: 64,621-133,201,316 HOXC6, LOH12CR2, 2452 more genes
    nsv3897722copy number variation1nstd102humanPathogenic GRCh37 chr12: 191,619-133,777,645 , GRCh38.p12 chr12: 82,453-133,201,059 HOXC6, 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 HOXC6, BTG1P1, 2451 more genes
    nsv3904719copy number variation1nstd102humanPathogenic GRCh37 chr12: 621,220-133,779,118 , GRCh38.p12 chr12: 512,054-133,202,532 HOXC6, OR5BT1P, 2441 more genes
    nsv3910529copy number variation1nstd102humanPathogenic NCBI36 chr12: 52,100,657-54,882,993 , GRCh38 chr12: 53,420,606-56,202,942 , GRCh37 chr12: 53,814,390-56,596,726 HOXC6, OR6C72P, 140 more genes
    nsv3919396copy number variation1nstd102humanLikely benign GRCh38 chr12: 53,841,686-54,136,856 , NCBI36 chr12: 52,521,737-52,816,907 , GRCh37 chr12: 54,235,470-54,530,640 HOXC6, HOXC8, 21 more genes
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