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Items: 1 to 20 of 239

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099175copy number variation1nstd231human GRCh38.p12 chr1: 6,492,665-9,894,222 , GRCh37 chr1: 6,552,725-9,954,280 RERE, CA6, 70 more genes
    nsv7098827copy number variation1nstd102humanPathogenic GRCh37 chr1: 4,481,271-20,530,242 , GRCh38.p12 chr1: 4,421,211-20,203,749 LOC107985467, LINC01777, 386 more genes
    nsv7096005copy number variation1nstd102humanUncertain significance GRCh37 chr1: 7,700,440-8,601,397 , GRCh38.p12 chr1: 7,640,380-8,541,338 RNU1-7P, PER3, 18 more genes
    nsv7058041inversion1nstd229human GRCh38 chr1: 1,845,355-9,534,096 , GRCh37.p13 chr1: 1,776,794-9,594,155 RPL37P9, TMEM52, 152 more genes
    nsv7057525inversion1nstd229human GRCh38 chr1: 7,829,944-15,116,659 , GRCh37.p13 chr1: 7,890,004-15,443,155 PEX14, RNU6-304P, 187 more genes
    nsv7054534inversion1nstd229human GRCh38 chr1: 2,972,403-10,562,308 , GRCh37.p13 chr1: 2,888,967-10,622,365 RN7SL731P, LOC105376682, 145 more genes
    nsv7052549inversion1nstd229human GRCh38 chr1: 8,322,830-13,737,741 , GRCh37.p13 chr1: 8,382,890-14,064,236 MIR4632, PLOD1, 166 more genes
    nsv7050952inversion1nstd229human GRCh38 chr1: 7,187,356-8,831,900 , GRCh37.p13 chr1: 7,247,416-8,891,959 RPL7P7, LOC107984915, 26 more genes
    nsv7047983inversion1nstd229human GRCh38 chr1: 5,346,988-12,521,611 , GRCh37.p13 chr1: 5,407,048-12,581,655 THAP3, UBIAD1, 165 more genes
    nsv7046461inversion1nstd229human GRCh38 chr1: 5,352,168-12,521,473 , GRCh37.p13 chr1: 5,412,228-12,581,517 LINC02606, C1orf127, 165 more genes
    nsv7044144inversion1nstd229human GRCh38 chr1: 6,762,728-10,175,549 , GRCh37.p13 chr1: 6,822,788-10,235,607 RPL7P11, LOC105376691, 68 more genes
    nsv6656127copy number variation1nstd229human GRCh38 chr1: 8,324,501-8,331,900 , GRCh37.p13 chr1: 8,384,561-8,391,960 SLC45A1
    nsv6656114copy number variation1nstd229human GRCh38 chr1: 8,301,219-8,343,585 , GRCh37.p13 chr1: 8,361,279-8,403,645 SLC45A1
    nsv6656064copy number variation1nstd229human GRCh38 chr1: 8,333,676-8,391,986 , GRCh37.p13 chr1: 8,393,736-8,452,046 RERE, SLC45A1
    nsv6656059copy number variation1nstd229human GRCh38 chr1: 8,317,514-8,317,756 , GRCh37.p13 chr1: 8,377,574-8,377,816 SLC45A1
    nsv6656048copy number variation1nstd229human GRCh38 chr1: 8,297,201-8,346,500 , GRCh37.p13 chr1: 8,357,261-8,406,560 SLC45A1
    nsv6655887copy number variation1nstd229human GRCh38 chr1: 8,338,428-8,339,287 , GRCh37.p13 chr1: 8,398,488-8,399,347 SLC45A1
    nsv6655619copy number variation1nstd229human GRCh38 chr1: 8,215,568-8,329,893 , GRCh37.p13 chr1: 8,275,628-8,389,953 RNU6-991P, LINC01714, 2 more genes
    nsv6637093copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,467-12,448,956 , GRCh38.p12 chr1: 914,087-12,388,897 VWA1, CEP104, 311 more genes
    nsv6636785copy number variation1nstd102humanPathogenic GRCh37 chr1: 6,758,933-19,287,770 , GRCh38.p12 chr1: 6,698,873-18,961,276 GPR157, MST1L, 313 more genes
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