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    Number of Variants: 10

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4456763copy number variation1nstd102humanPathogenic GRCh37 chr12: 77,737,623-94,330,526 , GRCh38.p12 chr12: 77,343,843-93,936,750 MRPL42, MIR1252, 162 more genes
    nsv3904242copy number variation1nstd102humanPathogenic GRCh37 chr12: 1-133,851,895 , GRCh38.p12 chr12: 45,740-133,265,309 MRPL42, RNA5SP369, 2454 more genes
    nsv3905447copy number variation2nstd102humanPathogenic GRCh37 chr12: 173,787-133,777,902 , GRCh38.p12 chr12: 64,621-133,201,316 MRPL42, LOH12CR2, 2452 more genes
    nsv3897722copy number variation1nstd102humanPathogenic GRCh37 chr12: 191,619-133,777,645 , GRCh38.p12 chr12: 82,453-133,201,059 MRPL42, 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 MRPL42, BTG1P1, 2451 more genes
    nsv3904719copy number variation1nstd102humanPathogenic GRCh37 chr12: 621,220-133,779,118 , GRCh38.p12 chr12: 512,054-133,202,532 MRPL42, OR5BT1P, 2441 more genes
    nsv3924338copy number variation1nstd102humanPathogenic NCBI36 chr12: 89,962,226-108,055,398 , GRCh38 chr12: 91,044,318-109,133,210 , GRCh37 chr12: 91,438,095-109,571,015 MRPL42, NUP37, 295 more genes
    nsv3911770copy number variation1nstd102humanLikely pathogenic NCBI36 chr12: 89,914,416-93,790,725 , GRCh37 chr12: 91,390,285-95,266,594 , GRCh38 chr12: 90,996,508-94,872,818 MRPL42, BTG1, 63 more genes
    nsv3904388copy number variation1nstd102humanUncertain significance GRCh37 chr12: 91,621,655-96,014,946 , GRCh38.p12 chr12: 91,227,878-95,621,170 MRPL42, LOC100287148, 76 more genes
    nsv3921474copy number variation1nstd102humanUncertain significance GRCh38 chr12: 93,374,113-94,267,175 , GRCh37 chr12: 93,767,889-94,660,951 , NCBI36 chr12: 92,292,020-93,185,082 MRPL42, PLXNC1, 16 more genes
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