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Items: 1 to 20 of 125

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5564524copy number variation1nstd102humanPathogenic GRCh38 chr19: 42,198,610-42,249,880 , GRCh37.p13 chr19: 42,702,762-42,754,032 ERF, ZNF526, 2 more genes
    nsv5564519copy number variation1nstd102humanPathogenic GRCh38 chr19: 41,987,984-42,252,574 , GRCh37.p13 chr19: 42,514,712-42,756,726 GRIK5, DEDD2, 8 more genes
    nsv5564317copy number variation1nstd102humanPathogenic GRCh38 chr19: 41,983,952-42,247,520 , GRCh37.p13 chr19: 42,514,712-42,751,672 GSK3A, ZNF574, 8 more genes
    nsv5564233copy number variation1nstd102humanPathogenic GRCh38 chr19: 42,032,860-42,297,536 , GRCh37.p13 chr19: 42,537,012-42,801,688 POU2F2, ERF, 9 more genes
    nsv5564232copy number variation1nstd102humanPathogenic GRCh38 chr19: 41,952,441-42,266,625 , GRCh37.p13 chr19: 42,514,712-42,770,777 CIC, ERF, 10 more genes
    nsv5562413sequence alteration1nstd206human GRCh38 chr19: 41,797,706-42,527,281 , GRCh37.p13 chr19: 42,514,712-43,031,433 MEGF8, LIPE, 34 more genes
    nsv5554149sequence alteration1nstd206human GRCh38 chr19: 41,749,279-42,444,786 , GRCh37.p13 chr19: 42,514,712-42,948,938 ERF, CEACAM6, 32 more genes
    nsv5532880copy number variation1nstd206human GRCh38 chr19: 42,200,430-42,202,080 , GRCh37.p13 chr19: 42,704,582-42,706,232 DEDD2
    nsv5285147copy number variation1nstd204human GRCh38.p13 chr19: 42,201,826-42,202,825 , GRCh37.p13 chr19: 42,705,978-42,706,977 DEDD2
    nsv5020518copy number variation1nstd200human GRCh38 chr19: 42,220,369-42,221,241 , GRCh37.p13 chr19: 42,724,521-42,725,393 ZNF526, DEDD2
    nsv4701913copy number variation1nstd195human GRCh38.p12 chr19: 42,014,849-42,223,099 , GRCh37 chr19: 42,519,001-42,727,251 GRIK5, POU2F2, 5 more genes
    nsv4667668copy number variation1nstd186human GRCh37 chr19: 42,704,579-42,706,232 , GRCh38.p12 chr19: 42,200,427-42,202,080 DEDD2
    nsv4624675copy number variation1nstd183human GRCh37 chr19: 42,704,579-42,706,232 , GRCh38.p12 chr19: 42,200,427-42,202,080 DEDD2
    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
    nsv4266170copy number variation1nstd166human GRCh37.p13 chr19: 42,720,900-42,726,000 , GRCh38.p12 chr19: 42,216,748-42,221,848 DEDD2, ZNF526
    nsv3921916copy number variation1nstd102humanPathogenic NCBI36 chr19: 47,126,886-48,337,448 , GRCh37 chr19: 42,514,712-43,645,608 , GRCh38 chr19: 41,930,894-43,141,456 PSG6, RABAC1, 42 more genes
    nsv3913730copy number variation1nstd102humanPathogenic NCBI36 chr19: 11,199,618-49,821,491 , GRCh37 chr19: 11,338,618-45,129,651 , GRCh38 chr19: 11,227,942-44,626,354 BCKDHA, ADGRE5, 1102 more genes
    nsv3912447copy number variation1nstd102humanPathogenic NCBI36 chr19: 42,502,119-47,934,680 , GRCh37 chr19: 37,810,279-43,242,840 , GRCh38 chr19: 37,319,377-42,738,688 MIR8077, TRI-TAT1-1, 233 more genes
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 ZNF321P, ZNF861P, 2443 more genes
    nsv3903203copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793 BABAM1, BEST2, 2426 more genes
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