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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097811copy number variation1nstd102humanPathogenic GRCh37 chr6: 135,679,250-135,754,414 , GRCh38.p12 chr6: 135,358,112-135,433,276 AHI1
    nsv7097419copy number variation1nstd102humanPathogenic GRCh37 chr6: 135,749,747-135,784,464 , GRCh38.p12 chr6: 135,428,609-135,463,326 AHI1
    nsv5673530copy number variation1nstd102humanPathogenic GRCh37 chr6: 135,749,761-135,784,450 , GRCh38.p12 chr6: 135,428,623-135,463,312 AHI1
    nsv4456715copy number variation2nstd102humanPathogenic, Likely pathogenic GRCh37 chr6: 135,710,693-135,735,779 , GRCh38.p12 chr6: 135,389,555-135,414,641 AHI1
    nsv3894662copy number variation3nstd102humanUncertain significance, Pathogenic GRCh37 chr6: 135,711,485-135,735,779 , GRCh38.p12 chr6: 135,390,347-135,414,641 AHI1
    nsv4456572copy number variation2nstd102humanPathogenic GRCh37 chr6: 135,721,284-135,730,984 , GRCh38.p12 chr6: 135,400,146-135,409,846 AHI1
    nsv3870726copy number variation1nstd102humanPathogenic GRCh38 chr6: 135,457,583-135,465,286 , GRCh37 chr6: 135,778,721-135,786,424 AHI1
    nsv5673678copy number variation1nstd102humanPathogenic GRCh37 chr6: 135,751,000-135,754,414 , GRCh38.p12 chr6: 135,429,862-135,433,276 AHI1
    nsv3887966copy number variation1nstd102humanPathogenic GRCh37 chr6: 135,751,020-135,754,394 , GRCh38 chr6: 135,429,882-135,433,256 AHI1
    nsv5381449copy number variation1nstd102humanPathogenic GRCh37 chr6: 135,769,428-135,769,613 , GRCh38.p12 chr6: 135,448,290-135,448,475 AHI1
    nsv4683217copy number variation2nstd102humanPathogenic, Likely pathogenic GRCh37 chr6: 135,679,250-135,679,345 , GRCh38.p12 chr6: 135,358,112-135,358,207 AHI1
    nsv6112748copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 135,715,893-135,732,702 , GRCh38.p12 chr6: 135,394,755-135,411,564 AHI1
    nsv3884944copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 135,715,894-135,732,702 , GRCh38 chr6: 135,394,756-135,411,564 AHI1
    nsv7093179copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 135,754,395-135,763,719 , GRCh38.p12 chr6: 135,433,257-135,442,581 AHI1
    nsv3876677copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 135,759,007-135,762,232 , GRCh38 chr6: 135,437,869-135,441,094 AHI1
    nsv7098696insertion1nstd102humanLikely benign GRCh38 chr6: 135,438,517-135,438,517 , GRCh37 chr6: 135,759,655-135,759,655 AHI1
    nsv6290499copy number variation1nstd102humanUncertain significance GRCh37 chr6: 135,679,326-135,748,304 , GRCh38.p12 chr6: 135,358,188-135,427,166 AHI1
    nsv3920619copy number variation1nstd102humanUncertain significance NCBI36 chr6: 135,721,087-135,752,589 , GRCh37.p13 chr6: 135,679,394-135,710,896 , GRCh38.p12 chr6: 135,358,256-135,389,758 AHI1
    nsv4675965copy number variation1nstd102humanUncertain significance GRCh37 chr6: 135,710,490-135,740,494 , GRCh38.p12 chr6: 135,389,352-135,419,356 AHI1
    nsv3892180copy number variation1nstd102humanUncertain significance GRCh37 chr6: 135,711,195-135,740,496 , GRCh38.p12 chr6: 135,390,057-135,419,358 AHI1
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