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Items: 1 to 20 of 203

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5973389insertion1nstd209human GRCh38 chr15: 91,017,368-91,017,368 , GRCh37.p13 chr15: 91,560,598-91,560,598 VPS33B
    nsv5593403copy number variation1nstd207human GRCh38 chr15: 91,014,973-91,015,107 , GRCh37.p13 chr15: 91,558,203-91,558,337 VPS33B
    nsv5524293copy number variation1nstd206human GRCh38 chr15: 91,019,946-91,024,220 , GRCh37.p13 chr15: 91,563,176-91,567,450 VPS33B, VPS33B-DT
    nsv5516380copy number variation1nstd206human GRCh38 chr15: 91,018,416-91,021,971 , GRCh37.p13 chr15: 91,561,646-91,565,201 VPS33B-DT, VPS33B
    nsv5318034copy number variation1nstd204human GRCh37.p13 chr15: 91,535,014-91,544,995 , GRCh38.p13 chr15: 90,991,784-91,001,765 VPS33B, PRC1
    nsv5308588copy number variation1nstd204human GRCh38.p13 chr15: 90,999,045-91,009,719 , GRCh37.p13 chr15: 91,542,275-91,552,949 VPS33B, LOC105370970
    nsv5279560copy number variation1nstd204human GRCh38.p13 chr15: 90,999,360-91,009,804 , GRCh37.p13 chr15: 91,542,590-91,553,034 VPS33B, LOC105370970
    nsv5277863copy number variation1nstd204human GRCh38.p13 chr15: 90,991,762-91,001,897 , GRCh37.p13 chr15: 91,534,992-91,545,127 PRC1, VPS33B
    nsv5273982copy number variation1nstd204human GRCh38.p13 chr15: 90,991,801-91,001,700 , GRCh37.p13 chr15: 91,535,031-91,544,930 PRC1, VPS33B
    nsv5009181copy number variation1nstd200human GRCh38 chr15: 90,949,020-91,019,180 , GRCh37.p13 chr15: 91,492,250-91,562,410 UNC45A, PRC1, 4 more genes
    nsv5002377copy number variation1nstd200human GRCh38 chr15: 90,996,244-90,997,677 , GRCh37.p13 chr15: 91,539,474-91,540,907 VPS33B
    nsv4863962copy number variation1nstd200human GRCh37 chr15: 91,542,543-91,552,747 , GRCh38.p12 chr15: 90,999,313-91,009,517 VPS33B, LOC105370970
    nsv4856334copy number variation1nstd200human GRCh37 chr15: 91,539,474-91,540,907 , GRCh38.p12 chr15: 90,996,244-90,997,677 VPS33B
    nsv4729092copy number variation1nstd102humanPathogenic GRCh37 chr15: 86,962,053-102,531,392 , GRCh38.p12 chr15: 86,418,822-101,981,189 CHD2, MIR11181, 272 more genes
    nsv4675149copy number variation1nstd102humanPathogenic GRCh37 chr15: 87,189,245-102,429,112 , GRCh38.p12 chr15: 86,646,014-101,888,909 TTLL13, LINC00052, 264 more genes
    nsv4627001copy number variation1nstd183human GRCh37 chr15: 91,563,226-91,567,483 , GRCh38.p12 chr15: 91,019,996-91,024,253 VPS33B-DT, VPS33B
    nsv4457347copy number variation1nstd102humanUncertain significance GRCh37 chr15: 91,276,782-91,550,953 , GRCh38.p12 chr15: 90,733,551-91,007,723 BLM, MAN2A2, 10 more genes
    nsv4456778copy number variation1nstd102humanPathogenic GRCh37 chr15: 91,229,877-93,677,014 , GRCh38.p12 chr15: 90,686,646-93,133,785 H2AZ2P1, MAN2A2, 44 more genes
    nsv4456430copy number variation1nstd102humanPathogenic GRCh37 chr15: 90,288,175-102,429,112 , GRCh38.p12 chr15: 89,744,944-101,888,909 IQGAP1, LOC400464, 210 more genes
    nsv4377776copy number variation1nstd173human GRCh37 chr15: 86,980,083-93,499,239 , GRCh38.p12 chr15: 86,436,852-92,956,009 , RNU6-1111P, 136 more genes
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