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Items: 1 to 20 of 451

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5906446copy number variation1nstd209human GRCh38 chr3: 52,657,721-52,658,043 , GRCh37.p13 chr3: 52,691,737-52,692,059 PBRM1
    nsv5899673copy number variation1nstd209human GRCh38 chr3: 52,620,076-52,620,144 , GRCh37.p13 chr3: 52,654,092-52,654,160 PBRM1
    nsv5895988copy number variation1nstd209human GRCh38 chr3: 52,675,821-52,676,155 , GRCh37.p13 chr3: 52,709,837-52,710,171 PBRM1
    nsv5836666copy number variation2nstd209human GRCh38 chr3: 52,596,409-52,597,808 , GRCh37.p13 chr3: 52,630,425-52,631,824 PBRM1
    nsv5836614copy number variation2nstd209human GRCh38 chr3: 52,596,184-52,597,608 , GRCh37.p13 chr3: 52,630,200-52,631,624 PBRM1
    nsv5687210mobile element insertion1nstd211human GRCh38 chr3: 52,674,644-52,674,644 , GRCh37.p13 chr3: 52,708,660-52,708,660 PBRM1
    nsv5681761mobile element insertion2nstd211human GRCh38 chr3: 52,551,671-52,551,671 , GRCh37.p13 chr3: 52,585,687-52,585,687 PBRM1, RNU6-856P
    nsv5675463mobile element insertion2nstd211human GRCh38 chr3: 52,664,430-52,664,430 , GRCh37.p13 chr3: 52,698,446-52,698,446 PBRM1
    nsv5572644copy number variation1nstd207human GRCh38 chr3: 52,675,821-52,676,155 , GRCh37.p13 chr3: 52,709,837-52,710,171 PBRM1
    nsv5561912sequence alteration1nstd206human GRCh38 chr3: 46,623,292-58,677,536 , GRCh37.p13 chr3: 46,664,782-58,663,263 , CDC25A, 327 more genes
    nsv5442654copy number variation1nstd206human GRCh38 chr3: 52,635,492-52,636,774 , GRCh37.p13 chr3: 52,669,508-52,670,790 PBRM1
    nsv5436510copy number variation1nstd206human GRCh38 chr3: 52,675,833-52,676,156 , GRCh37.p13 chr3: 52,709,849-52,710,172 PBRM1
    nsv5409748mobile element insertion1nstd206human GRCh38 chr3: 52,551,671-52,551,722 , GRCh37.p13 chr3: 52,585,687-52,585,738 PBRM1, RNU6-856P
    nsv5382615mobile element deletion2nstd186human GRCh37 chr3: 52,709,849-52,710,172 , GRCh38.p12 chr3: 52,675,833-52,676,156 PBRM1
    nsv5377522translocation1nstd200human GRCh38 chr3: 52,632,125-52,632,125 , GRCh38 chr3: 52,633,439-52,633,439 , GRCh37.p13 chr3: 52,666,141-52,666,141 , GRCh37.p13 chr3: 52,667,455-52,667,455 PBRM1
    nsv5305714copy number variation1nstd204human GRCh38.p13 chr3: 52,632,113-52,633,459 , GRCh37.p13 chr3: 52,666,129-52,667,475 PBRM1
    nsv5214126copy number variation1nstd204human GRCh38.p13 chr3: 52,675,801-52,676,100 , GRCh37.p13 chr3: 52,709,817-52,710,116 PBRM1
    nsv5208298mobile element deletion1nstd204human GRCh38.p13 chr3: 52,675,833-52,676,156 , GRCh37.p13 chr3: 52,709,849-52,710,172 PBRM1
    nsv5204396copy number variation1nstd204human GRCh38.p13 chr3: 52,590,784-52,592,783 , GRCh37.p13 chr3: 52,624,800-52,626,799 PBRM1
    nsv5197309mobile element insertion1nstd203human GRCh38 chr3: 52,664,233-52,664,235 , GRCh37.p13 chr3: 52,698,249-52,698,251 PBRM1
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