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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112770copy number variation1nstd102humanPathogenic GRCh37 chr15: 23,616,095-28,538,904 , GRCh38.p12 chr15: 23,370,948-28,293,758 LOC105370728, SNORD115-14, 144 more genes
    nsv5672660copy number variation1nstd102humanPathogenic GRCh38 chr15: 22,804,175-30,375,696 , GRCh37.p13 chr15: 23,564,855-30,667,899 TUBBP8, LOC102723564, 218 more genes
    nsv5557813sequence alteration1nstd206human GRCh38 chr15: 23,786,776-25,754,615 , GRCh37.p13 chr15: 24,031,923-25,999,762 , IPW, 110 more genes
    nsv5381773copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,833,525-27,193,380 , GRCh38.p12 chr15: 23,319,714-26,948,233 SNORD116-5, NPAP1, 139 more genes
    nsv5200367copy number variation1nstd102humanPathogenic GRCh37 chr15: 23,208,842-28,525,460 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 , GRCh38.p12 chr15: 23,319,714-28,280,314 SNORD115-27, LOC105370747, 246 more genes
    nsv5060035copy number variation1nstd102humanPathogenic GRCh37 chr15: 23,707,435-28,726,651 , GRCh38.p12 chr15: 23,462,288-28,481,505 PWAR4, SNORD116-18, 150 more genes
    nsv4708021copy number variation1nstd195human GRCh38.p12 chr15: 25,262,404-25,298,504 , GRCh37 chr15: 25,507,551-25,543,651 SNORD109B, SNORD115-48, 4 more genes
    nsv4685685copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,646,692-28,964,445 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 , GRCh38.p12 chr15: 23,319,714-28,719,299 MKRN3, RN7SL469P, 247 more genes
    nsv4685661copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,833,416-28,566,671 , GRCh38.p12 chr15: 23,319,714-28,321,525 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 LOC101060587, MPHOSPH10P8, 246 more genes
    nsv4685617copy number variation1nstd102humanPathogenic GRCh37 chr15: 23,579,300-28,447,626 , GRCh38.p12 chr15: 23,334,153-28,202,480 LOC105370726, SNORD115-12, 148 more genes
    nsv4684445copy number variation1nstd192human GRCh38.p12 chr15: 23,452,228-28,285,036 , GRCh37 chr15: 23,697,375-28,530,182 , GABRA5, 143 more genes
    nsv4684444copy number variation1nstd192human GRCh38.p12 chr15: 23,319,714-28,097,771 , GRCh37 chr15: 22,927,167-28,342,917 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 , APBA2, 258 more genes
    nsv4684443copy number variation1nstd192human GRCh38.p12 chr15: 23,319,714-27,732,633 , GRCh37 chr15: 22,853,785-27,977,779 , GABRA5, 150 more genes
    nsv4682484copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 24,811,185-26,026,370 , GRCh38.p12 chr15: 24,566,038-25,781,223 IPW, SNRPN, 100 more genes
    nsv4679090copy number variation1nstd189human GRCh37.p13 chr15: 23,621,774-28,536,236 , GRCh38.p12 chr15: 23,376,627-28,291,090 , GABRA5, 146 more genes
    nsv4678824copy number variation1nstd190human GRCh37.p13 chr15: 22,781,807-29,006,030 , GRCh38.p12 chr15: 23,319,714-28,760,884 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 , APBA2, 259 more genes
    nsv4678781copy number variation1nstd190human GRCh37.p13 chr15: 22,750,297-29,093,249 , GRCh38.p12 chr15: 23,319,714-28,848,103 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 , APBA2, 259 more genes
    nsv4678780copy number variation1nstd190human GRCh37.p13 chr15: 22,750,297-28,539,834 , GRCh38.p12 chr15: 23,319,714-28,294,688 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 , APBA2, 258 more genes
    nsv4678779copy number variation1nstd190human GRCh37.p13 chr15: 22,750,297-28,474,686 , GRCh38.p12 chr15: 23,319,714-28,229,540 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 , APBA2, 258 more genes
    nsv4678747copy number variation1nstd190human GRCh37.p13 chr15: 22,567,553-28,539,834 , GRCh38.p12 chr15: 22,279,602-28,294,688 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 , APBA2, 296 more genes
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