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Items: 1 to 20 of 391

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5939971copy number variation1nstd209human GRCh38 chr16: 69,568,170-69,572,390 , GRCh37.p13 chr16: 69,602,073-69,606,293 NFAT5
    nsv5936426copy number variation1nstd209human GRCh38 chr16: 69,623,566-69,624,287 , GRCh37.p13 chr16: 69,657,469-69,658,190 NFAT5
    nsv5879675copy number variation1nstd209human GRCh38 chr16: 69,701,946-69,702,945 , GRCh37.p13 chr16: 69,735,849-69,736,848 NFAT5
    nsv5872905copy number variation1nstd209human GRCh38 chr16: 69,568,184-69,570,151 , GRCh37.p13 chr16: 69,602,087-69,604,054 NFAT5
    nsv5701573mobile element insertion2nstd211human GRCh38 chr16: 69,606,490-69,606,490 , GRCh37.p13 chr16: 69,640,393-69,640,393 NFAT5
    nsv5694794mobile element insertion2nstd211human GRCh38 chr16: 69,652,775-69,652,775 , GRCh37.p13 chr16: 69,686,678-69,686,678 NFAT5
    nsv5532278copy number variation1nstd206human GRCh38 chr16: 69,677,060-69,924,863 , GRCh37.p13 chr16: 69,710,963-69,958,766 NQO1, NFAT5, 4 more genes
    nsv5524322copy number variation1nstd206human GRCh38 chr16: 69,618,332-69,618,417 , GRCh37.p13 chr16: 69,652,235-69,652,320 NFAT5
    nsv5519436copy number variation1nstd206human GRCh38 chr16: 69,568,370-69,568,441 , GRCh37.p13 chr16: 69,602,273-69,602,344 NFAT5
    nsv5517819copy number variation1nstd206human GRCh38 chr16: 69,660,289-69,660,350 , GRCh37.p13 chr16: 69,694,192-69,694,253 NFAT5
    nsv5419177mobile element insertion1nstd206human GRCh38 chr16: 69,606,490-69,606,541 , GRCh37.p13 chr16: 69,640,393-69,640,444 NFAT5
    nsv5365690translocation1nstd200human GRCh38 chr16: 69,661,261-69,661,261 , GRCh38 chr16: 69,669,733-69,669,733 , GRCh37.p13 chr16: 69,695,164-69,695,164 , GRCh37.p13 chr16: 69,703,636-69,703,636 NFAT5
    nsv5358312translocation1nstd200human GRCh38 chr16: 69,669,474-69,669,474 , GRCh38 chr16: 69,658,136-69,658,136 , GRCh37.p13 chr16: 69,703,377-69,703,377 , GRCh37.p13 chr16: 69,692,039-69,692,039 NFAT5
    nsv5263716copy number variation1nstd204human GRCh37.p13 chr16: 69,700,104-69,946,603 , GRCh38.p13 chr16: 69,666,201-69,912,700 NQO1, NFAT5, 4 more genes
    nsv5214465mobile element deletion1nstd204human GRCh38.p13 chr16: 69,685,777-69,686,070 , GRCh37.p13 chr16: 69,719,680-69,719,973 NFAT5
    nsv5189435mobile element insertion1nstd203human GRCh38 chr16: 69,597,557-69,597,571 , GRCh37.p13 chr16: 69,631,460-69,631,474 NFAT5
    nsv5157103mobile element insertion1nstd203human GRCh38 chr16: 69,606,477-69,606,490 , GRCh37.p13 chr16: 69,640,380-69,640,393 NFAT5
    nsv5156816mobile element insertion1nstd203human GRCh38 chr16: 69,644,130-69,644,149 , GRCh37.p13 chr16: 69,678,033-69,678,052 NFAT5
    nsv5154914mobile element insertion1nstd203human GRCh38 chr16: 69,691,557-69,691,566 , GRCh37.p13 chr16: 69,725,460-69,725,469 NFAT5
    nsv5154577mobile element insertion1nstd203human GRCh38 chr16: 69,658,682-69,658,682 , GRCh37.p13 chr16: 69,692,585-69,692,585 NFAT5
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