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Items: 1 to 20 of 243

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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
    nsv5898209copy number variation1nstd209human GRCh38 chr4: 143,826,755-144,057,657 , GRCh37.p13 chr4: 144,747,908-144,978,810 GYPB, GYPE, 4 more genes
    nsv5898208copy number variation1nstd209human GRCh38 chr4: 143,790,321-144,031,241 , GRCh37.p13 chr4: 144,711,474-144,952,394 GYPB, GYPE, 4 more genes
    nsv5838278copy number variation1nstd209human GRCh38 chr4: 143,817,103-143,819,736 , GRCh37.p13 chr4: 144,738,256-144,740,889 LOC105377458
    nsv5838277copy number variation1nstd209human GRCh38 chr4: 143,807,838-143,827,521 , GRCh37.p13 chr4: 144,728,991-144,748,674 LOC105377458
    nsv5837721copy number variation1nstd209human GRCh38 chr4: 143,820,712-143,835,758 , GRCh37.p13 chr4: 144,741,865-144,756,911 LOC105377458
    nsv5726359mobile element insertion1nstd211human GRCh38 chr4: 143,822,520-143,822,520 , GRCh37.p13 chr4: 144,743,673-144,743,673 LOC105377458
    nsv5692407mobile element insertion1nstd211human GRCh38 chr4: 143,817,372-143,817,372 , GRCh37.p13 chr4: 144,738,525-144,738,525 LOC105377458
    nsv5609247insertion1nstd207human GRCh38 chr4: 143,829,635-143,829,635 , GRCh37.p13 chr4: 144,750,788-144,750,788 LOC105377458
    nsv5581286copy number variation1nstd207human GRCh38 chr4: 143,793,109-144,034,014 , GRCh37.p13 chr4: 144,714,262-144,955,167 GYPB, GYPE, 4 more genes
    nsv5579030copy number variation1nstd207human GRCh38 chr4: 143,818,646-143,823,927 , GRCh37.p13 chr4: 144,739,799-144,745,080 LOC105377458
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5472238copy number variation1nstd206human GRCh38 chr4: 143,797,000-143,832,200 , GRCh37.p13 chr4: 144,718,153-144,753,353 LOC105377458
    nsv5465021copy number variation1nstd206human GRCh38 chr4: 143,817,381-144,015,381 , GRCh37.p13 chr4: 144,738,534-144,936,534 GYPB, GYPE, 4 more genes
    nsv5462606copy number variation1nstd206human GRCh38 chr4: 143,814,010-143,940,121 , GRCh37.p13 chr4: 144,735,163-144,861,274 GYPE, LOC100420464, 3 more genes
    nsv5454875copy number variation1nstd206human GRCh38 chr4: 143,785,901-143,822,520 , GRCh37.p13 chr4: 144,707,054-144,743,673 LOC105377458
    nsv4948516copy number variation1nstd200human GRCh38 chr4: 143,776,211-143,846,355 , GRCh37.p13 chr4: 144,697,364-144,767,508 LOC105377459, LOC105377458
    nsv4946118copy number variation1nstd200human GRCh38 chr4: 143,814,870-143,818,422 , GRCh37.p13 chr4: 144,736,023-144,739,575 LOC105377458
    nsv4946112copy number variation1nstd200human GRCh38 chr4: 143,581,290-143,929,130 , GRCh37.p13 chr4: 144,502,443-144,850,283 GYPE, FREM3, 5 more genes
    nsv4794545copy number variation1nstd200human GRCh37 chr4: 144,697,364-144,767,508 , GRCh38.p12 chr4: 143,776,211-143,846,355 LOC105377459, LOC105377458
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