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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112765copy number variation1nstd102humanPathogenic GRCh37 chr10: 118,247,181-135,435,319 , GRCh38.p12 chr10: 116,487,669-133,621,815 STK32C, LOC105378542, 266 more genes
    nsv5980446copy number variation1nstd102humanPathogenic GRCh37 chr10: 122,785,023-135,457,222 , GRCh38.p12 chr10: 121,025,510-133,643,718 LINC02641, CFAP46, 194 more genes
    nsv5971684insertion1nstd209human GRCh38 chr10: 121,577,159-121,577,159 , GRCh37.p13 chr10: 123,336,673-123,336,673 FGFR2
    nsv5918631copy number variation1nstd209human GRCh38 chr10: 121,142,744-121,483,785 , GRCh37.p13 chr10: 122,902,258-123,243,299 FGFR2, LINC01153, 3 more genes
    nsv5672603copy number variation1nstd102humanLikely pathogenic GRCh37 chr10: 119,302,758-124,813,305 , GRCh38.p12 chr10: 117,543,247-123,053,789 ACADSB, DMBT1, 84 more genes
    nsv5672528copy number variation1nstd102humanPathogenic GRCh37 chr10: 123,276,813-123,276,997 , GRCh38.p12 chr10: 121,517,299-121,517,483 FGFR2
    nsv5642571insertion2nstd207human GRCh38 chr10: 121,584,818-121,584,818 , GRCh37.p13 chr10: 123,344,332-123,344,332 FGFR2
    nsv5502529copy number variation1nstd206human GRCh38 chr10: 121,506,332-121,507,589 , GRCh37.p13 chr10: 123,265,846-123,267,103 FGFR2
    nsv5500345copy number variation1nstd206human GRCh38 chr10: 121,574,758-121,574,844 , GRCh37.p13 chr10: 123,334,272-123,334,358 FGFR2
    nsv5244287copy number variation1nstd204human GRCh38.p13 chr10: 121,569,168-121,571,409 , GRCh37.p13 chr10: 123,328,682-123,330,923 FGFR2
    nsv5123435mobile element insertion1nstd203human GRCh38 chr10: 121,548,245-121,548,279 , GRCh37.p13 chr10: 123,307,759-123,307,793 FGFR2
    nsv4977260copy number variation1nstd200human GRCh38 chr10: 121,575,936-121,576,748 , GRCh37.p13 chr10: 123,335,450-123,336,262 FGFR2
    nsv4848554copy number variation1nstd200human GRCh37 chr10: 122,902,257-123,243,302 , GRCh38.p12 chr10: 121,142,743-121,483,788 RN7SKP167, LOC105378522, 3 more genes
    nsv4833171copy number variation1nstd200human GRCh37 chr10: 123,329,025-123,330,777 , GRCh38.p12 chr10: 121,569,511-121,571,263 FGFR2
    nsv4830495copy number variation1nstd200human GRCh37 chr10: 123,248,772-123,252,498 , GRCh38.p12 chr10: 121,489,258-121,492,984 FGFR2
    nsv4755197insertion1nstd199human GRCh37 chr10: 123,343,891-123,343,891 , GRCh38.p12 chr10: 121,584,377-121,584,377 FGFR2
    nsv4730388copy number variation1nstd199human GRCh37 chr10: 123,343,891-123,344,131 , GRCh38.p12 chr10: 121,584,377-121,584,617 FGFR2
    nsv4675991copy number variation1nstd102humanPathogenic GRCh37 chr10: 119,996,339-135,427,143 , GRCh38.p12 chr10: 118,236,827-133,613,639 STK32C, LOC105378542, 237 more genes
    nsv4675857copy number variation1nstd102humanUncertain significance GRCh37 chr10: 123,232,922-124,638,514 , GRCh38.p12 chr10: 121,473,408-122,878,998 LOC105378525, HTRA1, 20 more genes
    nsv4573697mobile element insertion1nstd166human GRCh37.p13 chr10: 123,307,204-123,307,204 , GRCh38.p12 chr10: 121,547,690-121,547,690 FGFR2
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