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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3895325copy number variation1nstd102humanBenign GRCh37 chr18: 12,663,152-12,822,702 , GRCh38.p12 chr18: 12,663,153-12,822,703 PTPN2, PSMG2, 2 more genes
    nsv3905681copy number variation1nstd102humanUncertain significance GRCh37 chr18: 12,691,414-12,794,330 , GRCh38.p12 chr18: 12,691,415-12,794,331 PTPN2, PSMG2, 2 more genes
    nsv6314722copy number variation1nstd102humanPathogenic GRCh37 chr18: 1,262,334-53,254,751 , GRCh38.p12 chr18: 1,262,333-55,587,520 PTPN2, LOC107985176, 632 more genes
    nsv3916217copy number variation1nstd102humanPathogenic NCBI36 chr18: 4,275-16,783,904 , GRCh37.p13 chr18: 14,275-18,529,906 , GRCh38.p12 chr18: 14,275-20,949,945 PTPN2, LOC101927410, 276 more genes
    nsv4676141copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,226-18,529,578 , GRCh38.p12 chr18: 136,226-20,949,617 PTPN2, ANKRD12, 270 more genes
    nsv6290328copy number variation1nstd102humanPathogenic GRCh37 chr18: 10,501-15,410,398 , GRCh38.p12 chr18: 10,501-15,410,399 PTPN2, RNA5SP449, 275 more genes
    nsv7098917copy number variation1nstd102humanPathogenic GRCh37 chr18: 1-15,400,035 , GRCh38.p12 chr18: 10,001-15,400,036 PTPN2, RNU7-25P, 275 more genes
    nsv3905455copy number variation1nstd102humanPathogenic GRCh37 chr18: 13,034-15,375,878 , GRCh38.p12 chr18: 13,034-15,375,879 PTPN2, LOC100533852, 275 more genes
    nsv4676393copy number variation1nstd102humanPathogenic GRCh37 chr18: 13,034-15,330,525 , GRCh38.p12 chr18: 13,034-15,330,526 PTPN2, PRELID3A, 275 more genes
    nsv3898793copy number variation1nstd102humanPathogenic GRCh37 chr18: 14,316-15,328,499 , GRCh38.p12 chr18: 14,316-15,328,500 PTPN2, LOC100419892, 275 more genes
    nsv3907765copy number variation1nstd102humanPathogenic GRCh37 chr18: 1-15,157,836 , GRCh38.p12 chr18: 10,001-15,157,837 PTPN2, LOC105372003, 269 more genes
    nsv3896525copy number variation5nstd102humanPathogenic GRCh37 chr18: 136,226-15,198,990 , GRCh38.p12 chr18: 136,226-15,198,991 PTPN2, PRELID3A, 264 more genes
    nsv3897591copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,226-15,198,989 , GRCh38.p12 chr18: 136,226-15,198,990 PTPN2, LOC107985155, 264 more genes
    nsv4348774copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,226-15,175,005 , GRCh38.p12 chr18: 136,226-15,175,006 PTPN2, ANKRD62, 263 more genes
    nsv3908226copy number variation1nstd102humanPathogenic GRCh37 chr18: 13,034-15,026,309 , GRCh38.p12 chr18: 13,034-15,026,310 PTPN2, LOC105371975, 269 more genes
    nsv4676314copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,304-15,143,714 , GRCh38.p12 chr18: 136,304-15,143,715 PTPN2, EIF4A2P1, 263 more genes
    nsv3911263copy number variation1nstd102humanPathogenic GRCh37 chr18: 131,700-15,121,054 , NCBI36 chr18: 121,700-15,111,054 , GRCh38 chr18: 131,700-15,121,055 PTPN2, RNU6-324P, 263 more genes
    nsv3916675copy number variation1nstd102humanPathogenic GRCh37 chr18: 48,782-14,978,075 , NCBI36 chr18: 38,782-14,968,075 , GRCh38 chr18: 48,782-14,978,076 PTPN2, L3MBTL4, 265 more genes
    nsv3924580copy number variation1nstd102humanPathogenic GRCh38 chr18: 118,760-15,024,003 , GRCh37 chr18: 118,760-15,024,002 , NCBI36 chr18: 108,760-15,014,002 PTPN2, LOC105371951, 264 more genes
    nsv3890222copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,226-14,983,938 , GRCh38.p12 chr18: 136,226-14,983,939 PTPN2, LOC105371986, 261 more genes
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