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Items: 1 to 20 of 334

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112778copy number variation1nstd102humanPathogenic GRCh37 chr20: 51,799,648-62,916,626 , GRCh38.p12 chr20: 53,183,109-64,285,273 LINC01742, MTCO2P1, 253 more genes
    nsv5673181copy number variation1nstd102humanPathogenic GRCh37 chr20: 62,076,002-62,324,646 , GRCh38.p12 chr20: 63,444,649-63,693,293 PPDPF, LOC105372725, 13 more genes
    nsv5596464copy number variation1nstd207human GRCh38 chr20: 63,553,558-63,553,657 , GRCh37.p13 chr20: 62,184,911-62,185,010 FNDC11
    nsv5562694sequence alteration1nstd206human GRCh38 chr20: 63,525,502-63,937,515 , GRCh37.p13 chr20: 62,156,855-62,568,868 , STMN3, 26 more genes
    nsv5559866sequence alteration1nstd206human GRCh38 chr20: 62,865,770-63,725,218 , GRCh37.p13 chr20: 61,497,122-62,356,570 , PTK6, 46 more genes
    nsv5390124copy number variation1nstd186human GRCh37 chr20: 62,184,927-62,184,997 , GRCh38.p12 chr20: 63,553,574-63,553,644 FNDC11
    nsv5381809copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,510,452-62,315,381 , GRCh38.p12 chr20: 62,879,100-63,684,028 MIR3196, NKAIN4, 40 more genes
    nsv5381223copy number variation2nstd102humanUncertain significance GRCh37 chr20: 60,831,241-62,664,346 , GRCh38.p12 chr20: 62,256,185-64,032,993 KCNQ2-AS1, HAR1B, 100 more genes
    nsv5293467copy number variation1nstd204human GRCh38.p13 chr20: 62,966,101-64,149,200 , GRCh37.p13 chr20: 61,597,453-62,780,553 , ZGPAT, 72 more genes
    nsv5287878copy number variation1nstd204human GRCh38.p13 chr20: 63,068,801-63,693,400 , GRCh37.p13 chr20: 61,700,153-62,324,753 , BIRC7, 33 more genes
    nsv4854180copy number variation1nstd200human GRCh37 chr20: 62,184,927-62,184,997 , GRCh38.p12 chr20: 63,553,574-63,553,644 FNDC11
    nsv4736284copy number variation1nstd199human GRCh37 chr20: 62,184,905-62,185,006 , GRCh38.p12 chr20: 63,553,552-63,553,653 FNDC11
    nsv4730030copy number variation1nstd102humanUncertain significance GRCh37 chr20: 61,884,113-62,234,685 , GRCh38.p12 chr20: 63,252,761-63,603,332 LOC105372725, ARFGAP1, 19 more genes
    nsv4729876copy number variation1nstd102humanUncertain significance GRCh37 chr20: 62,052,925-62,318,983 , GRCh38.p12 chr20: 63,421,572-63,687,630 PTK6, RTEL1, 14 more genes
    nsv4729754copy number variation1nstd102humanUncertain significance GRCh37 chr20: 61,507,440-62,318,983 , GRCh38.p12 chr20: 62,876,088-63,687,630 DIDO1, LOC102723814, 41 more genes
    nsv4729740copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,975,605-62,915,555 , GRCh38.p12 chr20: 63,344,253-64,284,202 STMN3, KCNQ2-AS1, 53 more genes
    nsv4681029copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr20: 61,977,556-62,562,941 , GRCh38.p12 chr20: 63,346,204-63,931,588 RNU1-134P, MIR941-5, 35 more genes
    nsv4676218copy number variation1nstd102humanUncertain significance GRCh37 chr20: 62,090,403-62,319,007 , GRCh38.p12 chr20: 63,459,050-63,687,654 LOC105372725, PPDPF, 12 more genes
    nsv4676208copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,152,321-62,915,555 , GRCh38.p12 chr20: 62,555,114-64,284,202 GMEB2, LOC105372727, 94 more genes
    nsv4676181copy number variation1nstd102humanPathogenic GRCh37 chr20: 56,788,101-62,762,405 , GRCh38.p12 chr20: 58,213,045-64,131,052 LOC105372697, MIR647, 174 more genes
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