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Items: 1 to 20 of 233

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5020532copy number variation1nstd200human GRCh38 chr19: 42,424,141-42,427,054 , GRCh37.p13 chr19: 42,928,293-42,931,206 LIPE-AS1, CXCL17, 1 more genes
    nsv5020531copy number variation1nstd200human GRCh38 chr19: 42,413,060-42,415,454 , GRCh37.p13 chr19: 42,917,212-42,919,606 LIPE, LIPE-AS1
    nsv5020530copy number variation1nstd200human GRCh38 chr19: 42,403,637-42,406,297 , GRCh37.p13 chr19: 42,907,789-42,910,449 LIPE-AS1, LOC101930071, 1 more genes
    nsv5020529copy number variation1nstd200human GRCh38 chr19: 42,399,618-42,400,342 , GRCh37.p13 chr19: 42,903,770-42,904,494 LIPE, LIPE-AS1, 1 more genes
    nsv5020528copy number variation1nstd200human GRCh38 chr19: 42,394,037-42,401,009 , GRCh37.p13 chr19: 42,898,189-42,905,161 LIPE-AS1, LIPE, 1 more genes
    nsv4868458copy number variation1nstd200human GRCh37 chr19: 42,928,293-42,931,206 , GRCh38.p12 chr19: 42,424,141-42,427,054 LIPE, CXCL17, 1 more genes
    nsv4868457copy number variation1nstd200human GRCh37 chr19: 42,915,316-42,915,566 , GRCh38.p12 chr19: 42,411,164-42,411,414 LIPE-AS1, LIPE
    nsv4868456copy number variation1nstd200human GRCh37 chr19: 42,907,790-42,910,449 , GRCh38.p12 chr19: 42,403,638-42,406,297 LIPE, LIPE-AS1, 1 more genes
    nsv4868455copy number variation1nstd200human GRCh37 chr19: 42,903,770-42,904,494 , GRCh38.p12 chr19: 42,399,618-42,400,342 LIPE-AS1, LOC101930071, 1 more genes
    nsv4868454copy number variation1nstd200human GRCh37 chr19: 42,898,188-42,905,164 , GRCh38.p12 chr19: 42,394,036-42,401,012 LIPE-AS1, LOC101930071, 1 more genes
    nsv4715396copy number variation1nstd195human GRCh38.p12 chr19: 42,419,999-42,609,899 , GRCh37 chr19: 42,924,151-43,114,051 CEACAM1, CEACAM8, 7 more genes
    nsv4534722copy number variation1nstd166human GRCh37.p13 chr19: 42,930,999-43,263,000 , GRCh38.p12 chr19: 42,426,847-42,758,848 LIPE, CXCL17, 12 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
    nsv4267939copy number variation1nstd166human GRCh37.p13 chr19: 42,898,189-42,905,296 , GRCh38.p12 chr19: 42,394,037-42,401,144 LIPE, LIPE-AS1, 1 more genes
    nsv4266017copy number variation1nstd166human GRCh37.p13 chr19: 42,931,000-42,962,000 , GRCh38.p12 chr19: 42,426,848-42,457,848 LIPE-AS1, LIPE, 1 more genes
    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
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