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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5673473copy number variation1nstd102humanLikely benign GRCh37 chr3: 12,632,277-12,660,220 , GRCh38.p12 chr3: 12,590,778-12,618,721 RAF1
    nsv4683259copy number variation1nstd102humanUncertain significance GRCh37 chr3: 12,626,003-12,660,230 , GRCh38.p12 chr3: 12,584,504-12,618,731 RAF1
    nsv6311850copy number variation1nstd102humanUncertain significance GRCh37 chr3: 12,632,277-12,633,311 , GRCh38.p12 chr3: 12,590,778-12,591,812 RAF1
    nsv4682051copy number variation1nstd102humanUncertain significance GRCh37 chr3: 12,632,287-12,633,301 , GRCh38.p12 chr3: 12,590,788-12,591,802 RAF1
    nsv7097346copy number variation1nstd102humanUncertain significance GRCh37 chr7: 140,534,389-140,534,692 , GRCh38.p12 chr7: 140,834,589-140,834,892 BRAF
    nsv6312323copy number variation1nstd102humanUncertain significance GRCh37 chr7: 140,434,397-140,550,032 , GRCh38.p12 chr7: 140,734,597-140,850,232 BRAF
    nsv3880498copy number variation1nstd102humanUncertain significance GRCh38 chr7: 140,734,577-140,834,892 , GRCh37 chr7: 140,434,377-140,534,692 BRAF
    nsv3924125copy number variation1nstd102humanUncertain significance NCBI36 chr3: 12,608,362-12,680,118 , GRCh38 chr3: 12,591,863-12,663,619 , GRCh37 chr3: 12,633,362-12,705,118 RAF1
    nsv4455039copy number variation1nstd102humanUncertain significance GRCh38 chr3: 12,584,504-12,618,731 , GRCh37 chr3: 12,626,003-12,660,230 RAF1
    nsv4452220copy number variation1nstd102humanUncertain significance GRCh37 chr3: 12,626,013-12,660,235 , GRCh38.p12 chr3: 12,584,514-12,618,736 RAF1
    nsv7096930copy number variation1nstd102humanUncertain significance GRCh37 chr3: 12,629,070-12,660,220 , GRCh38.p12 chr3: 12,587,571-12,618,721 RAF1
    nsv3876425copy number variation1nstd102humanUncertain significance GRCh38 chr3: 12,590,726-12,618,797 , GRCh37 chr3: 12,632,225-12,660,296 RAF1
    nsv6311851copy number variation1nstd102humanUncertain significance GRCh37 chr3: 12,641,170-12,660,220 , GRCh38.p12 chr3: 12,599,671-12,618,721 RAF1
    nsv7096533copy number variation1nstd102humanUncertain significance GRCh37 chr3: 12,645,615-12,660,220 , GRCh38.p12 chr3: 12,604,116-12,618,721 RAF1
    nsv7096691copy number variation1nstd102humanUncertain significance GRCh37 chr3: 12,650,245-12,660,220 , GRCh38.p12 chr3: 12,608,746-12,618,721 RAF1
    nsv3879300copy number variation1nstd102humanUncertain significance GRCh37 chr3: 12,627,160-12,627,318 , GRCh38 chr3: 12,585,661-12,585,819 RAF1
    nsv3923071copy number variation1nstd102humanUncertain significance NCBI36 chr7: 140,051,304-140,189,374 , GRCh38 chr7: 140,705,035-140,843,105 , GRCh37 chr7: 140,404,835-140,542,905 BRAF, NDUFB2
    nsv7097486copy number variation1nstd102humanUncertain significance GRCh37 chr7: 140,624,346-140,624,503 , GRCh38.p12 chr7: 140,924,546-140,924,703 LOC105375536, BRAF
    nsv3874273copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 12,633,308-12,777,019 , GRCh38.p12 chr3: 12,591,809-12,735,520 RAF1, TMEM40, 1 more genes
    nsv3891073copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 140,616,125-140,740,863 , GRCh38.p12 chr7: 140,916,325-141,041,063 BRAF, MRPS33, 3 more genes
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