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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6119886copy number variation1nstd186human GRCh37 chr4: 147,207,661-147,208,136 , GRCh38.p12 chr4: 146,286,509-146,286,984 SLC10A7
    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
    nsv5963444insertion1nstd209human GRCh38 chr4: 146,430,027-146,430,027 , GRCh37.p13 chr4: 147,351,179-147,351,179 SLC10A7
    nsv5954881insertion1nstd209human GRCh38 chr4: 146,468,471-146,468,471 , GRCh37.p13 chr4: 147,389,623-147,389,623 SLC10A7
    nsv5906756copy number variation1nstd209human GRCh38 chr4: 146,286,228-146,286,703 , GRCh37.p13 chr4: 147,207,380-147,207,855 SLC10A7
    nsv5903770copy number variation1nstd209human GRCh38 chr4: 146,476,106-146,476,524 , GRCh37.p13 chr4: 147,397,258-147,397,676 SLC10A7
    nsv5903181copy number variation1nstd209human GRCh38 chr4: 146,401,108-146,409,879 , GRCh37.p13 chr4: 147,322,260-147,331,031 SLC10A7, MIR7849
    nsv5896233copy number variation1nstd209human GRCh38 chr4: 146,190,128-146,855,608 , GRCh37.p13 chr4: 147,111,280-147,776,760 POU4F2, LSM6, 7 more genes
    nsv5888127copy number variation1nstd209human GRCh38 chr4: 146,401,999-146,402,186 , GRCh37.p13 chr4: 147,323,151-147,323,338 SLC10A7
    nsv5887930copy number variation1nstd209human GRCh38 chr4: 146,429,654-146,430,022 , GRCh37.p13 chr4: 147,350,806-147,351,174 SLC10A7
    nsv5887635copy number variation1nstd209human GRCh38 chr4: 146,286,488-146,286,703 , GRCh37.p13 chr4: 147,207,640-147,207,855 SLC10A7
    nsv5838290copy number variation1nstd209human GRCh38 chr4: 146,500,619-146,532,645 , GRCh37.p13 chr4: 147,421,771-147,453,797 SLC10A7
    nsv5838289copy number variation1nstd209human GRCh38 chr4: 146,475,684-146,499,918 , GRCh37.p13 chr4: 147,396,836-147,421,070 SLC10A7
    nsv5838288copy number variation1nstd209human GRCh38 chr4: 146,392,023-146,423,182 , GRCh37.p13 chr4: 147,313,175-147,344,334 MIR7849, SLC10A7
    nsv5838027copy number variation2nstd209human GRCh38 chr4: 146,401,121-146,402,920 , GRCh37.p13 chr4: 147,322,273-147,324,072 SLC10A7
    nsv5838026copy number variation2nstd209human GRCh38 chr4: 146,401,021-146,409,787 , GRCh37.p13 chr4: 147,322,173-147,330,939 SLC10A7, MIR7849
    nsv5838025copy number variation1nstd209human GRCh38 chr4: 146,287,188-146,314,938 , GRCh37.p13 chr4: 147,208,340-147,236,090 SLC10A7, LOC105377472
    nsv5837737copy number variation1nstd209human GRCh38 chr4: 146,474,684-146,476,820 , GRCh37.p13 chr4: 147,395,836-147,397,972 SLC10A7
    nsv5837736copy number variation1nstd209human GRCh38 chr4: 146,332,192-146,366,650 , GRCh37.p13 chr4: 147,253,344-147,287,802 SLC10A7
    nsv5728750mobile element insertion2nstd211human GRCh38 chr4: 146,304,144-146,304,144 , GRCh37.p13 chr4: 147,225,296-147,225,296 SLC10A7
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