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Items: 1 to 20 of 172

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5905904copy number variation1nstd209human GRCh38 chr5: 16,455,734-16,458,182 , GRCh37.p13 chr5: 16,455,843-16,458,291 ZNF622
    nsv5841556copy number variation1nstd209human GRCh38 chr5: 16,455,811-16,458,476 , GRCh37.p13 chr5: 16,455,920-16,458,585 ZNF622
    nsv5724697mobile element insertion2nstd211human GRCh38 chr5: 16,464,200-16,464,200 , GRCh37.p13 chr5: 16,464,309-16,464,309 ZNF622
    nsv5560226mobile element insertion1nstd206human GRCh38 chr5: 16,464,200-16,464,251 , GRCh37.p13 chr5: 16,464,309-16,464,360 ZNF622
    nsv5381771copy number variation1nstd102humanPathogenic GRCh37 chr5: 22,149-29,048,823 , GRCh38.p12 chr5: 22,149-29,048,716 OTULINL, AKTIPP2, 317 more genes
    nsv5362123translocation1nstd200human GRCh38 chr5: 16,453,616-16,453,616 , GRCh38 chr5: 16,453,555-16,453,555 , GRCh37.p13 chr5: 16,453,664-16,453,664 , GRCh37.p13 chr5: 16,453,725-16,453,725 ZNF622
    nsv5179841mobile element insertion1nstd203human GRCh38 chr5: 16,464,186-16,464,200 , GRCh37.p13 chr5: 16,464,295-16,464,309 ZNF622
    nsv5166010mobile element insertion1nstd203human GRCh38 chr5: 16,464,193-16,464,200 , GRCh37.p13 chr5: 16,464,302-16,464,309 ZNF622
    nsv4685752copy number variation1nstd102humanPathogenic GRCh37 chr5: 71,904-22,078,969 , GRCh38.p12 chr5: 71,789-22,078,860 LINC01377, LOC100421308, 277 more genes
    nsv4674767copy number variation1nstd102humanUncertain significance GRCh37 chr5: 15,093,064-16,669,298 , GRCh38.p12 chr5: 15,092,955-16,669,189 RNA5SP178, LOC107986406, 18 more genes
    nsv4674161copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,576-23,364,376 , GRCh38.p12 chr5: 113,461-23,364,267 LOC102723561, LOC107986397, 287 more genes
    nsv4540540insertion1nstd166human GRCh37.p13 chr5: 16,464,295-16,464,295 , GRCh38.p12 chr5: 16,464,186-16,464,186 ZNF622
    nsv4456248copy number variation1nstd102humanUncertain significance GRCh37 chr5: 11,182,916-18,624,750 , GRCh38.p12 chr5: 11,182,804-18,624,641 OTULIN, LINC02218, 83 more genes
    nsv4436202copy number variation1nstd102humanUncertain significance GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379 RNU1-150P, RNU6-727P, 1757 more genes
    nsv4349271copy number variation1nstd102humanPathogenic GRCh37 chr5: 140,474-26,906,925 , GRCh38.p12 chr5: 140,359-26,906,816 MIR4636, LRRC14B, 304 more genes
    nsv3924736copy number variation1nstd102humanPathogenic NCBI36 chr5: 75,149-33,454,051 , GRCh38 chr5: 22,149-33,418,188 , GRCh37 chr5: 22,149-33,418,294 LOC105374678, ZFR, 369 more genes
    nsv3924496copy number variation1nstd102humanPathogenic GRCh37 chr5: 22,149-32,248,116 , NCBI36 chr5: 75,149-32,283,873 , GRCh38 chr5: 22,149-32,248,010 LOC105374678, MIR4278, 356 more genes
    nsv3923992copy number variation1nstd102humanPathogenic GRCh37 chr5: 50,093-46,115,086 , NCBI36 chr5: 103,093-46,150,843 , GRCh38 chr5: 49,978-46,114,984 LOC100130748, CDH10, 533 more genes
    nsv3923396copy number variation1nstd102humanPathogenic GRCh37 chr5: 22,149-27,188,057 , NCBI36 chr5: 75,149-27,223,814 , GRCh38 chr5: 22,149-27,187,950 LINC02899, TERLR1, 307 more genes
    nsv3923129copy number variation1nstd102humanPathogenic GRCh38 chr5: 22,149-16,584,575 , GRCh37 chr5: 22,149-16,584,684 , NCBI36 chr5: 75,149-16,637,684 AHRR, CTD-2154B17.1, 219 more genes
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