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Items: 1 to 20 of 960

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7143923copy number variation1nstd232human GRCh37.p13 chr3: 61,804,498-61,804,550 , GRCh38.p12 chr3: 61,818,824-61,818,876 PTPRG
    nsv7140941insertion1nstd232human GRCh37.p13 chr3: 61,666,419-61,666,419 , GRCh38.p12 chr3: 61,680,745-61,680,745 PTPRG
    nsv7055733inversion1nstd229human GRCh38 chr3: 62,059,496-62,127,924 , GRCh37.p13 chr3: 62,045,170-62,113,598 RNU2-10P, ID2B, 1 more genes
    nsv7055287inversion1nstd229human GRCh38 chr3: 61,912,915-61,919,891 , GRCh37.p13 chr3: 61,898,589-61,905,565 PTPRG
    nsv7054076inversion1nstd229human GRCh38 chr3: 61,734,906-61,992,267 , GRCh37.p13 chr3: 61,720,580-61,977,941 PTPRG, RPL10AP6
    nsv7051968inversion1nstd229human GRCh38 chr3: 56,944,702-65,952,705 , GRCh37.p13 chr3: 56,978,730-65,938,380 ILF2P1, ARHGEF3-AS1, 115 more genes
    nsv7051786inversion1nstd229human GRCh38 chr3: 62,286,572-62,286,737 , GRCh37.p13 chr3: 62,272,247-62,272,412 PTPRG-AS1, PTPRG
    nsv7050133inversion1nstd229human GRCh38 chr3: 62,109,497-62,127,497 , GRCh37.p13 chr3: 62,095,171-62,113,171 RNU2-10P, ID2B, 1 more genes
    nsv7048271inversion1nstd229human GRCh38 chr3: 59,959,176-65,947,271 , GRCh37.p13 chr3: 59,944,902-65,932,946 LOC105377124, RPS10P10, 63 more genes
    nsv7043821inversion1nstd229human GRCh38 chr3: 61,857,451-61,864,956 , GRCh37.p13 chr3: 61,843,125-61,850,630 PTPRG
    nsv7040610inversion1nstd229human GRCh38 chr3: 59,230,466-63,049,610 , GRCh37.p13 chr3: 59,216,192-63,035,286 FEZF2, CFAP20DC-DT, 26 more genes
    nsv7039673inversion1nstd229human GRCh38 chr3: 59,959,184-65,957,254 , GRCh37.p13 chr3: 59,944,910-65,942,929 PPIAP70, LOC105377114, 63 more genes
    nsv7038168inversion1nstd229human GRCh38 chr3: 61,851,237-61,857,563 , GRCh37.p13 chr3: 61,836,911-61,843,237 PTPRG
    nsv6718062copy number variation1nstd229human GRCh38 chr3: 62,096,832-62,097,405 , GRCh37.p13 chr3: 62,082,506-62,083,079 PTPRG
    nsv6717959copy number variation1nstd229human GRCh38 chr3: 62,024,225-62,024,381 , GRCh37.p13 chr3: 62,009,899-62,010,055 PTPRG
    nsv6716948copy number variation1nstd229human GRCh38 chr3: 61,657,170-61,661,360 , GRCh37.p13 chr3: 61,642,844-61,647,034 PTPRG
    nsv6716828copy number variation1nstd229human GRCh38 chr3: 61,624,960-61,630,170 , GRCh37.p13 chr3: 61,610,634-61,615,844 PTPRG
    nsv6716752copy number variation1nstd229human GRCh38 chr3: 61,871,601-61,881,800 , GRCh37.p13 chr3: 61,857,275-61,867,474 PTPRG
    nsv6716284copy number variation1nstd229human GRCh38 chr3: 61,665,762-61,667,740 , GRCh37.p13 chr3: 61,651,436-61,653,414 PTPRG
    nsv6716243copy number variation1nstd229human GRCh38 chr3: 61,621,403-61,664,689 , GRCh37.p13 chr3: 61,607,077-61,650,363 PTPRG
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