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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148242copy number variation1nstd102humanPathogenic GRCh38 chr15: 20,966,971-25,963,714 , GRCh37.p13 chr15: 21,172,300-26,208,861 LOC101269108, LOC107983983, 227 more genes
    nsv7148111copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,742,396-28,567,325 , GRCh38.p12 chr15: 23,319,714-28,322,179 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 SNORD116-18, PWAR4, 246 more genes
    nsv7148097copy number variation1nstd102humanPathogenic GRCh37 chr15: 23,605,427-28,566,579 , GRCh38.p12 chr15: 23,360,280-28,321,433 LOC107984770, SNORD115-31, 147 more genes
    nsv7137213copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,770,421-30,386,398 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 , GRCh38.p12 chr15: 23,319,714-30,094,195 TVP23BP1, SNORD115-1, 247 more genes
    nsv7137100copy number variation1nstd102humanPathogenic GRCh37 chr15: 23,684,691-28,566,579 , GRCh38.p12 chr15: 23,439,544-28,321,433 DMAC1P1, SNORD116-16, 142 more genes
    nsv7098883copy number variation1nstd102humanPathogenic GRCh37 chr15: 23,406,271-28,566,579 , GRCh38.p12 chr15: 23,319,714-28,321,433 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 LOC105370739, SNORD116-27, 246 more genes
    nsv7098730copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 22,833,523-25,223,593 , GRCh38.p12 chr15: 23,319,714-24,978,446 NDN, SNRPN, 30 more genes
    nsv7093407copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,833,525-28,544,662 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 , GRCh38.p12 chr15: 23,319,714-28,299,516 UBE2CP4, SERPINE4P, 246 more genes
    nsv7093400copy number variation1nstd102humanPathogenic GRCh37 chr15: 23,684,645-28,566,612 , GRCh38.p12 chr15: 23,439,498-28,321,466 SNORD115-45, SNORD107, 142 more genes
    nsv7065496inversion1nstd229human GRCh38 chr15: 20,672,644-28,900,286 , GRCh37.p13 chr15: 20,877,973-29,145,432 SNURF, LOC101060118, 290 more genes
    nsv7059943inversion1nstd229human GRCh38 chr15: 23,296,263-23,501,808 , GRCh37.p13 chr15: 23,564,855-23,746,955 LOC105370728, GOLGA8S, 10 more genes
    nsv6973232copy number variation1nstd229human GRCh38 chr15: 23,440,111-23,440,317 , GRCh37.p13 chr15: 23,685,258-23,685,464 GOLGA6L2
    nsv6973165copy number variation1nstd229human GRCh38 chr15: 23,199,056-28,429,484 , GRCh37.p13 chr15: 23,564,855-28,674,630 LOC102723564, SNORD115-2, 162 more genes
    nsv6969388copy number variation1nstd229human GRCh38 chr15: 22,643,175-24,846,430 , GRCh37.p13 chr15: 23,564,855-25,091,577 WHAMMP3, LOC105370732, 50 more genes
    nsv6969131copy number variation1nstd229human GRCh38 chr15: 22,744,959-28,819,371 , GRCh37.p13 chr15: 23,564,855-29,064,517 RNA5SP391, PDCD6IPP1, 195 more genes
    nsv6959362copy number variation1nstd229human GRCh38 chr15: 23,440,872-23,441,601 , GRCh37.p13 chr15: 23,686,019-23,686,748 GOLGA6L2
    nsv6637778copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,770,422-28,545,601 , GRCh38.p12 chr15: 23,319,714-28,300,455 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 LOC107984779, ULK4P1, 246 more genes
    nsv6637596copy number variation1nstd102humanPathogenic GRCh37 chr15: 23,290,787-28,560,269 , GRCh38.p12 chr15: 23,319,714-28,315,123 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 SNORD115-23, DEPDC1P1, 246 more genes
    nsv6637553copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,770,422-30,386,553 , GRCh38.p12 chr15: 23,319,714-30,094,350 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 FAN1, LOC105370751, 247 more genes
    nsv6637498copy number variation1nstd102humanPathogenic GRCh37 chr15: 23,670,891-28,561,671 , GRCh38.p12 chr15: 23,425,744-28,316,525 LOC107984770, SNORD115-34, 143 more genes
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