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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7143270copy number variation1nstd232human GRCh37.p13 chr10: 123,343,869-123,344,106 , GRCh38.p12 chr10: 121,584,355-121,584,592 FGFR2
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7098893copy number variation1nstd102humanPathogenic GRCh37 chr10: 122,610,933-135,439,810 , GRCh38.p12 chr10: 120,851,421-133,626,306 LOC105378571, DOCK1, 196 more genes
    nsv7093623copy number variation1nstd102humanUncertain significance GRCh37 chr10: 123,239,371-124,813,281 , GRCh38.p12 chr10: 121,479,857-123,053,765 TACC2, BTBD16, 25 more genes
    nsv7068192inversion1nstd229human GRCh38 chr10: 118,910,158-125,783,778 , GRCh37.p13 chr10: 120,669,670-127,472,347 CTBP2, RPS26P39, 114 more genes
    nsv6896505copy number variation1nstd229human GRCh38 chr10: 121,575,922-121,576,827 , GRCh37.p13 chr10: 123,335,436-123,336,341 FGFR2
    nsv6885727copy number variation1nstd229human GRCh38 chr10: 121,505,869-121,505,961 , GRCh37.p13 chr10: 123,265,383-123,265,475 FGFR2
    nsv6882060copy number variation1nstd229human GRCh38 chr10: 121,564,780-121,619,683 , GRCh37.p13 chr10: 123,324,294-123,379,197 FGFR2
    nsv6881009copy number variation1nstd229human GRCh38 chr10: 121,569,601-121,571,400 , GRCh37.p13 chr10: 123,329,115-123,330,914 FGFR2
    nsv6880438copy number variation1nstd229human GRCh38 chr10: 121,490,454-121,490,540 , GRCh37.p13 chr10: 123,249,968-123,250,054 FGFR2
    nsv6880252copy number variation1nstd229human GRCh38 chr10: 121,559,480-121,572,767 , GRCh37.p13 chr10: 123,318,994-123,332,281 FGFR2
    nsv6879944copy number variation1nstd229human GRCh38 chr10: 121,503,205-121,896,746 , GRCh37.p13 chr10: 123,262,719-123,656,261 LOC107984183, ATE1, 2 more genes
    nsv6879242copy number variation1nstd229human GRCh38 chr10: 121,484,942-121,719,153 , GRCh37.p13 chr10: 123,244,456-123,478,667 FGFR2, RPS15AP5, 1 more genes
    nsv6620169copy number variation1nstd224human GRCh37 chr10: 123,235,020-123,318,961 , GRCh38.p12 chr10: 121,475,506-121,559,447 FGFR2
    nsv6585886inversion1nstd223human GRCh38 chr10: 118,910,158-125,783,778 , GRCh37.p13 chr10: 120,669,670-127,472,347 LOC105378520, SPADH, 114 more genes
    nsv6438813copy number variation1nstd223human GRCh38 chr10: 121,569,201-121,571,700 , GRCh37.p13 chr10: 123,328,715-123,331,214 FGFR2
    nsv6437484copy number variation1nstd223human GRCh38 chr10: 121,597,101-121,599,300 , GRCh37.p13 chr10: 123,356,615-123,358,814 FGFR2
    nsv6314129copy number variation1nstd102humanPathogenic GRCh37 chr10: 117,019,650-125,217,066 , GRCh38.p12 chr10: 115,260,173-123,457,550 PDZD8, MIR3663HG, 122 more genes
    nsv6314085copy number variation1nstd102humanPathogenic GRCh37 chr10: 108,455,687-135,427,143 , GRCh38.p12 chr10: 106,695,929-133,613,639 LOC107984268, DPYSL4, 379 more genes
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