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Items: 1 to 20 of 139

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7063251inversion1nstd229human GRCh38 chr19: 28,671,265-29,069,367 , GRCh37.p13 chr19: 29,162,172-29,560,274 RNA5SP470, LOC102724958, 4 more genes
    nsv7016130copy number variation1nstd229human GRCh38 chr19: 28,366,801-29,069,400 , GRCh37.p13 chr19: 28,857,708-29,560,307 LOC105372349, LOC100420587, 6 more genes
    nsv7012800copy number variation1nstd229human GRCh38 chr19: 28,848,801-29,336,200 , GRCh37.p13 chr19: 29,339,708-29,827,107 LINC01532, UQCRFS1, 6 more genes
    nsv7010495copy number variation1nstd229human GRCh38 chr19: 28,234,202-29,141,491 , GRCh37.p13 chr19: 28,725,109-29,632,398 LOC102724908, LINC01532, 6 more genes
    nsv7007067copy number variation1nstd229human GRCh38 chr19: 28,961,373-29,290,066 , GRCh37.p13 chr19: 29,452,280-29,780,973 VSTM2B-DT, UQCRFS1-DT, 6 more genes
    nsv7005429copy number variation1nstd229human GRCh38 chr19: 28,956,435-29,334,441 , GRCh37.p13 chr19: 29,447,342-29,825,348 UQCRFS1, RN7SL340P, 6 more genes
    nsv7002945copy number variation1nstd229human GRCh38 chr19: 28,615,551-29,086,191 , GRCh37.p13 chr19: 29,106,458-29,577,098 RNA5SP470, LOC102724958, 5 more genes
    nsv7002052copy number variation1nstd229human GRCh38 chr19: 28,963,510-28,966,622 , GRCh37.p13 chr19: 29,454,417-29,457,529 LINC00906, LOC102724958
    nsv7000547copy number variation1nstd229human GRCh38 chr19: 28,672,591-29,133,152 , GRCh37.p13 chr19: 29,163,498-29,624,059 MAN1A2P1, LINC01532, 4 more genes
    nsv6999032copy number variation1nstd229human GRCh38 chr19: 28,323,519-29,150,055 , GRCh37.p13 chr19: 28,814,426-29,640,962 LINC01532, LOC102724908, 6 more genes
    nsv6528879copy number variation1nstd223human GRCh38 chr19: 28,965,201-28,966,400 , GRCh37.p13 chr19: 29,456,108-29,457,307 LINC00906
    nsv6527526copy number variation1nstd223human GRCh38 chr19: 28,925,173-32,768,942 , GRCh37.p13 chr19: 29,416,080-33,259,848 DPY19L3, CCNE1, 50 more genes
    nsv6526233copy number variation1nstd223human GRCh38 chr19: 28,377,231-29,769,380 , GRCh37.p13 chr19: 28,868,138-30,260,287 LINC01532, C19orf12, 16 more genes
    nsv6290300copy number variation1nstd102humanPathogenic GRCh37 chr19: 19,546,923-41,313,229 , GRCh38.p12 chr19: 19,436,114-40,807,324 ZNF420, LOC105372330, 574 more genes
    nsv5519664copy number variation1nstd206human GRCh38 chr19: 28,965,815-28,966,884 , GRCh37.p13 chr19: 29,456,722-29,457,791 , LINC00906, 1 more genes
    nsv5518123copy number variation1nstd206human GRCh38 chr19: 28,480,549-29,115,795 , GRCh37.p13 chr19: 28,971,456-29,606,702 , LINC00906, 7 more genes
    nsv5024519copy number variation1nstd200human GRCh38 chr19: 28,925,173-32,768,971 , GRCh37.p13 chr19: 29,416,080-33,259,877 , LOC105372355, 53 more genes
    nsv5020201copy number variation1nstd200human GRCh38 chr19: 28,965,815-28,966,884 , GRCh37.p13 chr19: 29,456,722-29,457,791 , LOC102724958, 1 more genes
    nsv5020164copy number variation1nstd200human GRCh38 chr19: 28,377,231-29,769,380 , GRCh37.p13 chr19: 28,868,138-30,260,287 , LINC00906, 18 more genes
    nsv4861140copy number variation1nstd200human GRCh37 chr19: 29,456,722-29,457,791 , GRCh38.p12 chr19: 28,965,815-28,966,884 , LOC102724958, 1 more genes
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