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Items: 1 to 20 of 258

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5893716copy number variation1nstd209human GRCh38 chr3: 49,053,161-49,053,306 , GRCh37.p13 chr3: 49,090,594-49,090,739 QRICH1
    nsv5890607copy number variation1nstd209human GRCh38 chr3: 49,050,088-49,053,337 , GRCh37.p13 chr3: 49,087,521-49,090,770 QRICH1
    nsv5890264copy number variation1nstd209human GRCh38 chr3: 49,063,852-49,064,027 , GRCh37.p13 chr3: 49,101,285-49,101,460 QRICH1
    nsv5836600copy number variation1nstd209human GRCh38 chr3: 49,049,484-49,050,852 , GRCh37.p13 chr3: 49,086,917-49,088,285 QRICH1
    nsv5836317copy number variation1nstd209human GRCh38 chr3: 49,051,153-49,053,252 , GRCh37.p13 chr3: 49,088,586-49,090,685 QRICH1
    nsv5686065mobile element insertion1nstd211human GRCh38 chr3: 49,087,839-49,087,839 , GRCh37.p13 chr3: 49,125,272-49,125,272 QRICH1
    nsv5673729copy number variation1nstd102humanPathogenic GRCh37 chr3: 48,507,870-50,340,407 , GRCh38.p12 chr3: 48,466,471-50,302,976 SEMA3B-AS1, GNAT1, 87 more genes
    nsv5561912sequence alteration1nstd206human GRCh38 chr3: 46,623,292-58,677,536 , GRCh37.p13 chr3: 46,664,782-58,663,263 , CDC25A, 327 more genes
    nsv5453222copy number variation1nstd206human GRCh38 chr3: 49,063,852-49,064,028 , GRCh37.p13 chr3: 49,101,285-49,101,461 QRICH1
    nsv5452784copy number variation1nstd206human GRCh38 chr3: 49,036,138-49,038,325 , GRCh37.p13 chr3: 49,073,571-49,075,758 QRICH1
    nsv5451762copy number variation1nstd206human GRCh38 chr3: 49,059,025-49,060,257 , GRCh37.p13 chr3: 49,096,458-49,097,690 QRICH1
    nsv5442266copy number variation1nstd206human GRCh38 chr3: 49,039,071-49,043,343 , GRCh37.p13 chr3: 49,076,504-49,080,776 QRICH1
    nsv5441452copy number variation1nstd206human GRCh38 chr3: 49,041,670-49,042,137 , GRCh37.p13 chr3: 49,079,103-49,079,570 QRICH1
    nsv5377505translocation1nstd200human GRCh38 chr3: 49,039,071-49,039,071 , GRCh38 chr3: 49,043,343-49,043,343 , GRCh37.p13 chr3: 49,080,776-49,080,776 , GRCh37.p13 chr3: 49,076,504-49,076,504 QRICH1
    nsv5219687copy number variation1nstd204human GRCh38.p13 chr3: 49,084,991-49,087,793 , GRCh37.p13 chr3: 49,122,424-49,125,226 QRICH1
    nsv5215892copy number variation1nstd204human GRCh38.p13 chr3: 49,084,391-49,090,726 , GRCh37.p13 chr3: 49,121,824-49,128,159 QRICH1
    nsv5211134copy number variation1nstd204human GRCh38.p13 chr3: 48,639,801-49,381,300 , GRCh37.p13 chr3: 48,677,234-49,418,733 MIR6890, IHO1, 31 more genes
    nsv5066604mobile element insertion1nstd203human GRCh38 chr3: 49,060,189-49,060,206 , GRCh37.p13 chr3: 49,097,622-49,097,639 QRICH1
    nsv5037434inversion1nstd200human GRCh38 chr3: 5,031,119-56,902,223 , GRCh37.p13 chr3: 5,072,804-56,936,251 , IRAK2, 925 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
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