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Items: 1 to 20 of 175

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5531521copy number variation1nstd206human GRCh38 chr19: 37,629,367-37,629,689 , GRCh37.p13 chr19: 38,120,268-38,120,590 ZFP30
    nsv5525371copy number variation1nstd206human GRCh38 chr19: 37,633,944-37,634,051 , GRCh37.p13 chr19: 38,124,845-38,124,952 ZFP30
    nsv5516497copy number variation1nstd206human GRCh38 chr19: 37,467,633-37,640,567 , GRCh37.p13 chr19: 37,958,535-38,131,468 ZNF571-AS1, MTND5P45, 9 more genes
    nsv5178560mobile element insertion1nstd203human GRCh38 chr19: 37,636,479-37,636,491 , GRCh37.p13 chr19: 38,127,380-38,127,392 ZFP30
    nsv5027823copy number variation1nstd200human GRCh38 chr19: 37,563,805-37,732,131 , GRCh37.p13 chr19: 38,054,707-38,223,032 ZNF540, ZNF571, 8 more genes
    nsv5024604copy number variation1nstd200human GRCh38 chr19: 37,627,360-37,637,907 , GRCh37.p13 chr19: 38,118,261-38,128,808 ZFP30
    nsv4868256copy number variation1nstd200human GRCh37 chr19: 38,127,888-38,128,591 , GRCh38.p12 chr19: 37,636,987-37,637,690 ZFP30
    nsv4868255copy number variation1nstd200human GRCh37 chr19: 38,054,706-38,223,032 , GRCh38.p12 chr19: 37,563,804-37,732,131 MTND5P45, MTND4P41, 8 more genes
    nsv4865152copy number variation1nstd200human GRCh37 chr19: 38,118,261-38,128,808 , GRCh38.p12 chr19: 37,627,360-37,637,907 ZFP30
    nsv4715509copy number variation1nstd195human GRCh37 chr19: 37,827,901-38,232,451 , GRCh38.p12 chr19: 37,336,999-37,741,550 ZNF527, ZNF540, 15 more genes
    nsv4679943copy number variation1nstd189human GRCh37.p13 chr19: 37,838,926-38,764,481 , GRCh38.p12 chr19: 37,348,024-38,273,841 DPF1, SPINT2, 31 more genes
    nsv4676151copy number variation1nstd102humanLikely benign GRCh37 chr19: 37,820,245-38,150,396 , GRCh38.p12 chr19: 37,329,343-37,659,495 ZNF569, ZNF570, 11 more genes
    nsv4633336copy number variation1nstd183human GRCh37 chr19: 37,950,721-38,260,982 , GRCh38.p12 chr19: 37,459,819-37,770,342 ZNF793-AS1, MTND4P41, 13 more genes
    nsv4516161mobile element insertion1nstd166human GRCh37.p13 chr19: 38,133,137-38,133,137 , GRCh38.p12 chr19: 37,642,236-37,642,236 ZFP30
    nsv4457372copy number variation1nstd102humanPathogenic GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575 ZNF461, LOC101927572, 735 more genes
    nsv4436633complex substitution1nstd102humanUncertain significance GRCh38.p12 chr19: 36,183,403-38,162,322 , GRCh37 chr19: 36,674,305-38,652,962 ZNF146, ZFP30, 60 more genes
    nsv4267081copy number variation1nstd166human GRCh37.p13 chr19: 38,118,261-38,128,808 , GRCh38.p12 chr19: 37,627,360-37,637,907 ZFP30
    nsv4266587copy number variation1nstd166human GRCh37.p13 chr19: 38,063,569-38,156,021 , GRCh38.p12 chr19: 37,572,667-37,665,120 ZFP30, ZNF571, 4 more genes
    nsv3920617copy number variation1nstd102humanUncertain significance GRCh37 chr19: 37,598,298-38,170,622 , NCBI36 chr19: 42,290,138-42,862,462 , GRCh38 chr19: 37,107,396-37,679,721 ZNF570, ZNF383, 18 more genes
    nsv3919296copy number variation1nstd102humanPathogenic NCBI36 chr19: 34,844,605-43,297,203 , GRCh37 chr19: 30,152,765-38,605,363 , GRCh38 chr19: 29,661,858-38,114,723 UBA2, ZNF529, 241 more genes
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