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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    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
    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
    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
    nsv7075933inversion1nstd229human GRCh38 chr15: 27,763,634-29,945,003 , GRCh37.p13 chr15: 28,008,780-30,237,206 RN7SL719P, ENTREP2, 39 more genes
    nsv7074171inversion1nstd229human GRCh38 chr15: 27,576,188-29,433,618 , GRCh37.p13 chr15: 27,821,334-29,725,822 MPHOSPH10P7, RN7SL238P, 34 more genes
    nsv7069807inversion1nstd229human GRCh38 chr15: 28,247,887-28,655,501 , GRCh37.p13 chr15: 28,493,033-28,900,647 LOC101059997, MIR4509-2, 17 more genes
    nsv7067542inversion1nstd229human GRCh38 chr15: 23,549,781-28,456,830 , GRCh37.p13 chr15: 23,794,928-28,701,976 SNORD115-34, LOC107984787, 148 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
    nsv7065294inversion1nstd229human GRCh38 chr15: 27,010,857-29,330,650 , GRCh37.p13 chr15: 27,256,004-29,622,854 GABRG3-AS1, HERC2P1, 40 more genes
    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
    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
    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
    nsv6637399copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,770,422-28,545,355 , GRCh38.p12 chr15: 23,319,714-28,300,209 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 DNM1P28, MIR4508, 246 more genes
    nsv6637197copy number variation1nstd102humanPathogenic GRCh37 chr15: 28,540,415-32,446,830 , GRCh38.p12 chr15: 28,295,269-32,154,629 RN7SL238P, DEPDC1P1, 90 more genes
    nsv6634429copy number variation1nstd102humanPathogenic GRCh37 chr15: 20,739,497-28,566,579 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 , GRCh38.p12 chr15: 20,534,259-28,321,433 OR11J7P, SNORD115-21, 364 more genes
    nsv6595355inversion1nstd223human GRCh38 chr15: 28,146,412-30,832,660 , GRCh37.p13 chr15: 28,391,558-31,124,863 CHRFAM7A, RN7SL673P, 73 more genes
    nsv6590184inversion1nstd223human GRCh38 chr15: 23,199,052-28,487,721 , GRCh37.p13 chr15: 23,564,855-28,732,867 , MIR4715, 164 more genes
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