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Items: 1 to 20 of 135

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5528549copy number variation1nstd206human GRCh38 chr19: 37,769,337-37,821,913 , GRCh37.p13 chr19: 38,259,977-38,312,553 ZNF573, LOC644554, 4 more genes
    nsv5322112copy number variation1nstd204human GRCh38.p13 chr19: 37,787,923-37,790,196 , GRCh37.p13 chr19: 38,278,563-38,280,836 LOC728533
    nsv5027835copy number variation1nstd200human GRCh38 chr19: 37,784,488-37,829,771 , GRCh37.p13 chr19: 38,275,128-38,320,411 LOC644554, LOC728533, 4 more genes
    nsv5027833copy number variation1nstd200human GRCh38 chr19: 37,782,874-37,789,829 , GRCh37.p13 chr19: 38,273,514-38,280,469 LOC728533
    nsv4868260copy number variation1nstd200human GRCh37 chr19: 38,273,514-38,280,469 , GRCh38.p12 chr19: 37,782,874-37,789,829 LOC728533
    nsv4730007copy number variation1nstd102humanUncertain significance GRCh37 chr19: 38,243,156-38,570,829 , GRCh38.p12 chr19: 37,752,516-38,080,189 LOC728853, LOC105372394, 10 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
    nsv4676402copy number variation1nstd102humanUncertain significance GRCh37 chr19: 38,203,613-38,575,729 , GRCh38.p12 chr19: 37,712,712-38,085,089 LOC107985301, WDR87, 11 more genes
    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
    nsv4419844copy number variation1nstd174human GRCh37 chr19: 38,259,770-38,320,814 , GRCh38.p12 chr19: 37,769,130-37,830,174 ZNF573, LOC644554, 5 more genes
    nsv4257750copy number variation1nstd166human GRCh37.p13 chr19: 38,186,310-38,285,620 , GRCh38.p12 chr19: 37,695,409-37,794,980 LOC728533, ZNF573, 1 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
    nsv3916007copy number variation1nstd102humanPathogenic GRCh37 chr19: 30,162,231-38,393,630 , NCBI36 chr19: 34,854,071-43,085,470 , GRCh38 chr19: 29,671,324-37,902,990 MAG, RNU6-967P, 238 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
    nsv3909857copy number variation1nstd102humanUncertain significance GRCh37 chr19: 36,475,577-38,399,402 , GRCh38.p12 chr19: 35,984,675-37,908,762 ZNF790, ZNF571-AS1, 72 more genes
    nsv3909018copy number variation1nstd102humanUncertain significance GRCh37 chr19: 38,278,995-38,745,778 , GRCh38.p12 chr19: 37,788,355-38,255,138 SIPA1L3, LOC105372394, 13 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
    nsv3903447copy number variation1nstd102humanBenign GRCh37 chr19: 38,219,241-38,397,213 , GRCh38.p12 chr19: 37,728,340-37,906,573 LOC105372394, LOC100128948, 9 more genes
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