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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097217copy number variation1nstd102humanUncertain significance GRCh37 chr3: 9,908,818-10,085,568 , GRCh38.p12 chr3: 9,867,134-10,043,884 EMC3, PRRT3, 14 more genes
    nsv7096686copy number variation1nstd102humanPathogenic GRCh37 chr3: 10,108,063-10,114,567 , GRCh38.p12 chr3: 10,066,379-10,072,883 FANCD2
    nsv7096684copy number variation1nstd102humanPathogenic GRCh37 chr3: 10,080,953-10,085,558 , GRCh38.p12 chr3: 10,039,269-10,043,874 FANCD2
    nsv7096530copy number variation1nstd102humanPathogenic GRCh37 chr3: 10,130,113-10,133,956 , GRCh38.p12 chr3: 10,088,429-10,092,272 FANCD2OS, FANCD2
    nsv7096528copy number variation1nstd102humanPathogenic GRCh37 chr3: 10,094,051-11,078,652 , GRCh38.p12 chr3: 10,052,367-11,036,966 LINC00606, MIR378B, 19 more genes
    nsv7096432copy number variation1nstd102humanPathogenic GRCh37 chr3: 10,127,476-10,136,978 , GRCh38.p12 chr3: 10,085,792-10,095,294 FANCD2OS, FANCD2
    nsv7055847inversion1nstd229human GRCh38 chr3: 5,111,802-11,290,661 , GRCh37.p13 chr3: 5,153,487-11,332,347 GHRLOS, LHFPL4, 96 more genes
    nsv7042755inversion1nstd229human GRCh38 chr3: 8,982,205-12,221,239 , GRCh37.p13 chr3: 9,023,889-12,262,739 SYN2, MTCO1P5, 74 more genes
    nsv6717366copy number variation1nstd229human GRCh38 chr3: 10,077,128-10,077,161 , GRCh37.p13 chr3: 10,118,812-10,118,845 FANCD2
    nsv6716466copy number variation1nstd229human GRCh38 chr3: 10,031,645-10,036,218 , GRCh37.p13 chr3: 10,073,329-10,077,902 FANCD2, RNU6-670P
    nsv6716092copy number variation1nstd229human GRCh38 chr3: 10,078,920-10,248,061 , GRCh37.p13 chr3: 10,120,604-10,289,745 VHL, FANCD2OS, 4 more genes
    nsv6715869copy number variation1nstd229human GRCh38 chr3: 9,686,801-10,627,600 , GRCh37.p13 chr3: 9,728,485-10,669,285 FANCD2OS, CRELD1, 40 more genes
    nsv6708961copy number variation1nstd229human GRCh38 chr3: 10,083,101-10,103,479 , GRCh37.p13 chr3: 10,124,785-10,145,163 FANCD2, FANCD2OS
    nsv6707174copy number variation1nstd229human GRCh38 chr3: 10,063,188-10,065,740 , GRCh37.p13 chr3: 10,104,872-10,107,424 FANCD2
    nsv6705199copy number variation1nstd229human GRCh38 chr3: 10,101,484-10,103,581 , GRCh37.p13 chr3: 10,143,168-10,145,265 FANCD2OS, FANCD2
    nsv6703019copy number variation1nstd229human GRCh38 chr3: 10,029,812-10,032,309 , GRCh37.p13 chr3: 10,071,496-10,073,993 FANCD2
    nsv6702654copy number variation1nstd229human GRCh38 chr3: 10,010,601-10,032,600 , GRCh37.p13 chr3: 10,052,285-10,074,284 MARK2P2, FANCD2, 2 more genes
    nsv6702167copy number variation1nstd229human GRCh38 chr3: 10,101,483-10,106,105 , GRCh37.p13 chr3: 10,143,167-10,147,789 FANCD2OS, FANCD2
    nsv6698744copy number variation1nstd229human GRCh38 chr3: 10,083,301-10,510,500 , GRCh37.p13 chr3: 10,124,985-10,552,184 MIR885, IRAK2, 12 more genes
    nsv6698201copy number variation1nstd229human GRCh38 chr3: 10,041,317-10,045,091 , GRCh37.p13 chr3: 10,083,001-10,086,775 FANCD2
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