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Items: 1 to 20 of 262

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5975998inversion1nstd209human GRCh38 chr22: 15,410,359-15,841,527 , GRCh37.p13 chr22: 16,136,436-16,567,604 , YME1L1P1, 16 more genes
    nsv5972124insertion1nstd209human GRCh38 chr22: 15,750,083-15,750,083 , GRCh37.p13 chr22: 16,227,880-16,227,880 GRAMD4P2, PSLNR
    nsv5958061copy number variation1nstd209human GRCh38 chr22: 15,747,920-15,747,970 , GRCh37.p13 chr22: 16,229,993-16,230,043 PSLNR
    nsv5714192mobile element insertion1nstd211human GRCh38 chr22: 15,763,898-15,763,898 , GRCh37.p13 chr22: 16,214,065-16,214,065 , PSLNR
    nsv5695088mobile element insertion1nstd211human GRCh38 chr22: 15,756,890-15,756,890 , GRCh37.p13 chr22: 16,221,073-16,221,073 PSLNR
    nsv5672062inversion1nstd207human GRCh38 chr22: 15,576,910-15,904,656 , GRCh37.p13 chr22: 16,074,203-16,401,053 , POTEH, 12 more genes
    nsv5604430copy number variation1nstd207human GRCh38 chr22: 15,745,951-15,746,001 , GRCh37.p13 chr22: 16,231,962-16,232,012 PSLNR
    nsv5298954copy number variation1nstd204human GRCh38.p13 chr22: 15,745,648-15,748,893 , GRCh37.p13 chr22: 16,229,070-16,232,315 PSLNR, GRAMD4P2
    nsv5298439copy number variation1nstd204human GRCh38.p13 chr22: 15,738,401-15,744,900 , GRCh37.p13 chr22: 16,233,063-16,239,562 PSLNR
    nsv5297220copy number variation1nstd204human GRCh38.p13 chr22: 15,746,001-15,758,000 , GRCh37.p13 chr22: 16,219,963-16,231,962 GRAMD4P2, PSLNR
    nsv5297116copy number variation1nstd204human GRCh38.p13 chr22: 15,777,701-15,779,000 , GRCh37.p13 chr22: 16,198,963-16,200,262 PSLNR
    nsv5296883copy number variation1nstd204human GRCh38.p13 chr22: 15,738,201-15,741,800 , GRCh37.p13 chr22: 16,236,163-16,239,762 PSLNR
    nsv5294895copy number variation1nstd204human GRCh38.p13 chr22: 15,758,401-15,762,200 , GRCh37.p13 chr22: 16,215,763-16,219,562 PSLNR
    nsv5293952copy number variation1nstd204human GRCh38.p13 chr22: 15,753,401-15,755,700 , GRCh37.p13 chr22: 16,222,263-16,224,562 PSLNR
    nsv5293464copy number variation1nstd204human GRCh38.p13 chr22: 15,760,301-15,762,300 , GRCh37.p13 chr22: 16,215,663-16,217,662 PSLNR
    nsv5292881copy number variation1nstd204human GRCh38.p13 chr22: 15,741,501-15,750,300 , GRCh37.p13 chr22: 16,227,663-16,236,462 PSLNR, GRAMD4P2
    nsv5292580copy number variation1nstd204human GRCh38.p13 chr22: 15,733,301-15,753,200 , GRCh37.p13 chr22: 16,224,763-16,244,662 PSLNR, GRAMD4P2
    nsv5291766copy number variation1nstd204human GRCh38.p13 chr22: 15,738,201-15,740,000 , GRCh37.p13 chr22: 16,237,963-16,239,762 PSLNR
    nsv5289863copy number variation1nstd204human GRCh38.p13 chr22: 15,765,901-15,808,700 , GRCh37.p13 chr22: 16,169,263-16,212,062 , PSLNR, 2 more genes
    nsv5287879copy number variation1nstd204human GRCh38.p13 chr22: 15,742,401-15,755,700 , GRCh37.p13 chr22: 16,222,263-16,235,562 GRAMD4P2, PSLNR
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