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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148201copy number variation1nstd102humanPathogenic GRCh38 chr3: 93,979,547-124,774,010 , GRCh37.p13 chr3: 93,698,391-124,492,857 NECTIN3, H2BP3, 418 more genes
    nsv7146195copy number variation1nstd232human GRCh37.p13 chr3: 111,552,876-111,552,934 , GRCh38.p12 chr3: 111,834,029-111,834,087 PHLDB2, PLCXD2, 1 more genes
    nsv7141874copy number variation1nstd232human GRCh37.p13 chr3: 111,551,541-111,551,665 , GRCh38.p12 chr3: 111,832,694-111,832,818 PHLDB2, PLCXD2, 1 more genes
    nsv7138678copy number variation1nstd232human GRCh37.p13 chr3: 111,553,042-111,553,092 , GRCh38.p12 chr3: 111,834,195-111,834,245 PHLDB2, PLCXD2, 1 more genes
    nsv7098849copy number variation1nstd102humanPathogenic GRCh37 chr3: 110,943,783-115,859,912 , GRCh38.p12 chr3: 111,224,936-116,141,065 ATG3, SIDT1, 81 more genes
    nsv7051524inversion1nstd229human GRCh38 chr3: 110,492,556-118,654,181 , GRCh37.p13 chr3: 110,211,403-118,373,028 MIR8076, ZBTB20-AS4, 106 more genes
    nsv7048929inversion1nstd229human GRCh38 chr3: 111,696,461-111,701,746 , GRCh37.p13 chr3: 111,415,308-111,420,593 PLCXD2
    nsv7047895inversion1nstd229human GRCh38 chr3: 111,834,358-111,837,229 , GRCh37.p13 chr3: 111,553,205-111,556,076 PLCXD2, LOC105374040, 1 more genes
    nsv7046343inversion1nstd229human GRCh38 chr3: 108,261,187-113,011,016 , GRCh37.p13 chr3: 107,980,034-112,729,863 LOC105374041, DIMT1P1, 69 more genes
    nsv7042841inversion1nstd229human GRCh38 chr3: 104,903,601-112,515,639 , GRCh37.p13 chr3: 104,622,445-112,234,486 MTND4P16, CD47, 94 more genes
    nsv7039416inversion1nstd229human GRCh38 chr3: 111,765,090-113,399,244 , GRCh37.p13 chr3: 111,483,937-113,118,091 SLC9C1, TAGLN3, 35 more genes
    nsv6715566copy number variation1nstd229human GRCh38 chr3: 111,816,416-111,830,080 , GRCh37.p13 chr3: 111,535,263-111,548,927 LOC105374040, PLCXD2, 1 more genes
    nsv6715293copy number variation1nstd229human GRCh38 chr3: 111,702,101-111,719,200 , GRCh37.p13 chr3: 111,420,948-111,438,047 PLCXD2
    nsv6715097copy number variation1nstd229human GRCh38 chr3: 111,752,460-111,752,557 , GRCh37.p13 chr3: 111,471,307-111,471,404 PLCXD2, PHLDB2
    nsv6714422copy number variation1nstd229human GRCh38 chr3: 111,830,601-111,850,100 , GRCh37.p13 chr3: 111,549,448-111,568,947 PLCXD2, PHLDB2, 1 more genes
    nsv6712051copy number variation1nstd229human GRCh38 chr3: 111,762,847-111,788,944 , GRCh37.p13 chr3: 111,481,694-111,507,791 PLCXD2, PHLDB2, 1 more genes
    nsv6711694copy number variation1nstd229human GRCh38 chr3: 111,806,719-111,810,373 , GRCh37.p13 chr3: 111,525,566-111,529,220 PLCXD2, PHLDB2, 1 more genes
    nsv6711343copy number variation1nstd229human GRCh38 chr3: 111,828,867-111,836,444 , GRCh37.p13 chr3: 111,547,714-111,555,291 PLCXD2, PHLDB2, 1 more genes
    nsv6710912copy number variation1nstd229human GRCh38 chr3: 111,763,675-111,849,356 , GRCh37.p13 chr3: 111,482,522-111,568,203 PHLDB2, LOC105374040, 2 more genes
    nsv6710367copy number variation1nstd229human GRCh38 chr3: 111,805,458-111,805,887 , GRCh37.p13 chr3: 111,524,305-111,524,734 PHLDB2, PLCXD2, 1 more genes
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