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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6290519copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 43,903,696-43,910,856 , GRCh38 chr15: 43,611,498-43,618,658 STRC
    nsv3873666copy number variation1nstd102humanUncertain significance GRCh38 chr15: 43,609,245-43,609,394 , GRCh37 chr15: 43,901,443-43,901,592 STRC
    nsv4727862copy number variation2nstd197human GRCh38.p12 chr15: 43,607,864-43,610,437 , GRCh37 chr15: 43,900,062-43,902,635 STRC
    nsv3884972copy number variation1nstd102humanUncertain significance GRCh37 chr15: 43,900,061-43,901,532 , GRCh38 chr15: 43,607,863-43,609,334 STRC
    nsv3873642copy number variation1nstd102humanUncertain significance GRCh38 chr15: 43,609,248-43,609,314 , GRCh37 chr15: 43,901,446-43,901,512 STRC
    esv2098654copy number variation1estd194human NCBI36 chr15: 41,685,102-41,685,103 , GRCh37.p13 chr15: 43,897,810-43,897,811 , GRCh38.p12 chr15: 43,605,612-43,605,613 STRC
    nsv5271390copy number variation1nstd204human GRCh38.p13 chr15: 43,615,801-43,622,800 , GRCh37.p13 chr15: 43,907,999-43,914,998 STRC
    nsv5278363copy number variation1nstd204human GRCh38.p13 chr15: 43,610,001-43,613,600 , GRCh37.p13 chr15: 43,902,199-43,905,798 STRC
    nsv5274883copy number variation1nstd204human GRCh38.p13 chr15: 43,607,701-43,609,500 , GRCh37.p13 chr15: 43,899,899-43,901,698 STRC
    nsv4623223copy number variation1nstd183human GRCh37 chr15: 43,906,393-43,906,439 , GRCh38.p12 chr15: 43,614,195-43,614,241 STRC
    nsv1139629copy number variation1nstd106human GRCh37 chr15: 43,900,000-43,911,500 , GRCh38.p12 chr15: 43,607,802-43,619,302 STRC
    esv3368106copy number variation1estd59human NCBI36 chr15: 41,694,952-41,699,950 , GRCh37.p13 chr15: 43,907,660-43,912,658 , GRCh38.p12 chr15: 43,615,462-43,620,460 STRC
    nsv5659295insertion1nstd207human GRCh38 chr15: 43,604,103-43,604,103 , GRCh37.p13 chr15: 43,896,301-43,896,301 STRC
    nsv5646083insertion1nstd207human GRCh38 chr15: 43,600,232-43,600,232 , GRCh37.p13 chr15: 43,892,430-43,892,430 STRC
    nsv94591insertion1nstd6human NCBI35 chr15: 41,690,530-41,690,530 , GRCh37.p13 chr15: 43,903,238-43,903,238 , GRCh38.p12 chr15: 43,611,040-43,611,040 STRC
    nsv1779590short tandem repeat20nstd128human GRCh37 chr15: 43,903,199-43,903,237 , GRCh38.p12 chr15: 43,611,001-43,611,039 STRC
    nsv5059985copy number variation1nstd102humanPathogenic GRCh37 chr15: 43,893,593-43,901,532 , GRCh38 chr15: 43,601,395-43,609,334 STRC, RNU6-554P
    nsv1398354copy number variation1nstd102humanPathogenic GRCh37 chr15: 43,892,732-43,897,597 , GRCh38 chr15: 43,600,534-43,605,399 STRC, RNU6-554P
    nsv1398105copy number variation1nstd102humanPathogenic GRCh38 chr15: 43,600,750-43,603,601 , GRCh37 chr15: 43,892,948-43,895,799 STRC, RNU6-554P
    nsv1398305copy number variation2nstd102humanUncertain significance, Pathogenic GRCh38 chr15: 43,600,534-43,601,014 , GRCh37 chr15: 43,892,732-43,893,212 STRC, RNU6-554P
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