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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112754copy number variation1nstd102humanPathogenic GRCh37 chr4: 131,303,317-168,722,402 , GRCh38.p12 chr4: 130,382,162-167,801,251 MIR3139, CLGN, 407 more genes
    nsv5958422insertion1nstd209human GRCh38 chr4: 165,459,117-165,459,117 , GRCh37.p13 chr4: 166,380,269-166,380,269 CPE
    nsv5890564copy number variation1nstd209human GRCh38 chr4: 165,482,250-165,486,197 , GRCh37.p13 chr4: 166,403,402-166,407,349 CPE
    nsv5838410copy number variation1nstd209human GRCh38 chr4: 165,482,750-165,485,555 , GRCh37.p13 chr4: 166,403,902-166,406,707 CPE
    nsv5728418mobile element insertion1nstd211human GRCh38 chr4: 165,465,512-165,465,512 , GRCh37.p13 chr4: 166,386,664-166,386,664 CPE
    nsv5725190mobile element insertion1nstd211human GRCh38 chr4: 165,449,976-165,449,976 , GRCh37.p13 chr4: 166,371,128-166,371,128 CPE
    nsv5718582mobile element insertion1nstd211human GRCh38 chr4: 165,448,211-165,448,211 , GRCh37.p13 chr4: 166,369,363-166,369,363 CPE
    nsv5715578mobile element insertion2nstd211human GRCh38 chr4: 165,460,240-165,460,240 , GRCh37.p13 chr4: 166,381,392-166,381,392 CPE
    nsv5684362mobile element insertion1nstd211human GRCh38 chr4: 165,485,452-165,485,452 , GRCh37.p13 chr4: 166,406,604-166,406,604 CPE
    nsv5628465insertion1nstd207human GRCh38 chr4: 165,382,105-165,382,105 , GRCh37.p13 chr4: 166,303,257-166,303,257 CPE
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5560524mobile element insertion1nstd206human GRCh38 chr4: 165,460,240-165,460,288 , GRCh37.p13 chr4: 166,381,392-166,381,440 CPE
    nsv5467254copy number variation1nstd206human GRCh38 chr4: 165,397,005-165,397,946 , GRCh37.p13 chr4: 166,318,157-166,319,098 CPE
    nsv5462541copy number variation1nstd206human GRCh38 chr4: 165,483,708-165,483,806 , GRCh37.p13 chr4: 166,404,860-166,404,958 CPE
    nsv5381776copy number variation1nstd102humanPathogenic GRCh37 chr4: 157,771,352-172,496,278 , GRCh38.p12 chr4: 156,850,200-171,575,127 LOC107986326, LOC107986240, 144 more genes
    nsv5353417translocation1nstd200human GRCh38 chr4: 165,482,447-165,482,447 , GRCh38 chr4: 165,481,688-165,481,688 , GRCh37.p13 chr4: 166,403,599-166,403,599 , GRCh37.p13 chr4: 166,402,840-166,402,840 CPE
    nsv5182519mobile element insertion1nstd203human GRCh38 chr4: 165,427,413-165,427,429 , GRCh37.p13 chr4: 166,348,565-166,348,581 CPE
    nsv5171933mobile element insertion1nstd203human GRCh38 chr4: 165,460,226-165,460,240 , GRCh37.p13 chr4: 166,381,378-166,381,392 CPE
    nsv5099259mobile element insertion1nstd203human GRCh38 chr4: 165,412,731-165,412,739 , GRCh37.p13 chr4: 166,333,883-166,333,891 CPE
    nsv5092743mobile element insertion1nstd203human GRCh38 chr4: 165,461,188-165,461,210 , GRCh37.p13 chr4: 166,382,340-166,382,362 CPE
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