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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137778copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr11: 108,225,602-108,239,827 , GRCh38.p12 chr11: 108,354,875-108,369,100 ATM, C11orf65
    nsv6137716copy number variation1nstd102humanUncertain significance GRCh37 chr11: 108,114,846-108,239,827 , GRCh38.p12 chr11: 108,244,119-108,369,100 C11orf65, ATM
    nsv6112751copy number variation1nstd102humanPathogenic GRCh37 chr11: 108,233,807-108,245,056 , GRCh38.p12 chr11: 108,363,080-108,374,329 C11orf65, ATM
    nsv6112749copy number variation1nstd102humannot provided GRCh37 chr11: 108,235,811-108,239,828 , GRCh38.p12 chr11: 108,365,084-108,369,101 C11orf65, ATM
    nsv5980431copy number variation1nstd102humanUncertain significance GRCh37 chr11: 108,225,602-108,236,198 , GRCh38.p12 chr11: 108,354,875-108,365,471 C11orf65, ATM
    nsv5980373copy number variation2nstd102humanPathogenic GRCh37 chr11: 108,098,332-108,236,255 , GRCh38.p12 chr11: 108,227,605-108,365,528 C11orf65, ATM
    nsv5918104copy number variation1nstd209human GRCh38 chr11: 104,190,618-110,044,159 , GRCh37.p13 chr11: 104,061,346-109,914,884 , CARD18, 71 more genes
    nsv5851070copy number variation1nstd209human GRCh38 chr11: 108,358,923-108,374,657 , GRCh37.p13 chr11: 108,229,650-108,245,384 C11orf65, ATM
    nsv5722104mobile element insertion1nstd211human GRCh38 chr11: 108,237,920-108,237,920 , GRCh37.p13 chr11: 108,108,647-108,108,647 ATM
    nsv5707077mobile element insertion2nstd211human GRCh38 chr11: 108,333,998-108,333,998 , GRCh37.p13 chr11: 108,204,725-108,204,725 ATM, C11orf65
    nsv5700017mobile element insertion2nstd211human GRCh38 chr11: 108,262,068-108,262,068 , GRCh37.p13 chr11: 108,132,795-108,132,795 ATM
    nsv5697584mobile element insertion1nstd211human GRCh38 chr11: 108,366,158-108,366,158 , GRCh37.p13 chr11: 108,236,885-108,236,885 ATM, C11orf65
    nsv5674283delins1nstd102humanPathogenic GRCh37 chr11: 108,167,652-108,168,064 , GRCh38 chr11: 108,296,925-108,297,337 ATM
    nsv5674272insertion1nstd102humanPathogenic GRCh37 chr11: 108,153,575-108,153,575 , GRCh38 chr11: 108,282,848-108,282,848 ATM
    nsv5674267insertion2nstd102humanPathogenic GRCh37 chr11: 108,150,293-108,150,293 , GRCh38 chr11: 108,279,566-108,279,566 ATM
    nsv5674255insertion1nstd102humanPathogenic GRCh37 chr11: 108,141,788-108,141,788 , GRCh38 chr11: 108,271,061-108,271,061 ATM
    nsv5672777copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 108,196,027-108,199,975 , GRCh38.p12 chr11: 108,325,300-108,329,248 ATM, C11orf65
    nsv5672776copy number variation1nstd102humanPathogenic GRCh37 chr11: 108,196,027-108,196,281 , GRCh38.p12 chr11: 108,325,300-108,325,554 ATM, C11orf65
    nsv5672775copy number variation1nstd102humanPathogenic GRCh37 chr11: 108,186,540-108,218,102 , GRCh38.p12 chr11: 108,315,813-108,347,375 C11orf65, ATM
    nsv5672774copy number variation1nstd102humanPathogenic GRCh37 chr11: 108,178,614-108,178,721 , GRCh38.p12 chr11: 108,307,887-108,307,994 ATM, C11orf65
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