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Items: 1 to 20 of 196

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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
    nsv5966881copy number variation1nstd209human GRCh38 chr20: 63,050,462-63,050,511 , GRCh37.p13 chr20: 61,681,814-61,681,863 LINC01749, LINC01056
    nsv5959690copy number variation1nstd209human GRCh38 chr20: 63,037,040-63,037,089 , GRCh37.p13 chr20: 61,668,392-61,668,441 LINC01749, LINC00029, 1 more genes
    nsv5956863copy number variation1nstd209human GRCh38 chr20: 63,045,225-63,045,303 , GRCh37.p13 chr20: 61,676,577-61,676,655 LINC01749, LINC01056
    nsv5955257copy number variation1nstd209human GRCh38 chr20: 63,037,844-63,037,915 , GRCh37.p13 chr20: 61,669,196-61,669,267 LINC01056, LINC01749
    nsv5949909copy number variation1nstd209human GRCh38 chr20: 63,050,762-63,050,833 , GRCh37.p13 chr20: 61,682,114-61,682,185 LINC01056, LINC01749
    nsv5668735insertion1nstd207human GRCh38 chr20: 63,049,159-63,049,159 , GRCh37.p13 chr20: 61,680,511-61,680,511 LINC01749, LINC01056
    nsv5603873copy number variation1nstd207human GRCh38 chr20: 63,050,462-63,050,511 , GRCh37.p13 chr20: 61,681,814-61,681,863 LINC01749, LINC01056
    nsv5602629copy number variation1nstd207human GRCh38 chr20: 63,051,206-63,051,279 , GRCh37.p13 chr20: 61,682,558-61,682,631 LINC01749, LINC01056
    nsv5594010copy number variation1nstd207human GRCh38 chr20: 63,045,225-63,045,303 , GRCh37.p13 chr20: 61,676,577-61,676,655 LINC01749, LINC01056
    nsv5559866sequence alteration1nstd206human GRCh38 chr20: 62,865,770-63,725,218 , GRCh37.p13 chr20: 61,497,122-62,356,570 , PTK6, 46 more genes
    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
    nsv5350560translocation1nstd200human GRCh38 chr20: 63,045,789-63,045,789 , GRCh38 chr20: 63,035,125-63,035,125 , GRCh37.p13 chr20: 61,666,477-61,666,477 , GRCh37.p13 chr20: 61,677,141-61,677,141 LINC01749, LINC00029, 1 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
    nsv5025820copy number variation1nstd200human GRCh38 chr20: 63,047,681-63,129,564 , GRCh37.p13 chr20: 61,679,033-61,760,916 LINC01056, LOC105376996, 4 more genes
    nsv5022575copy number variation1nstd200human GRCh38 chr20: 63,018,208-63,076,079 , GRCh37.p13 chr20: 61,649,560-61,707,431 LINC01749, LINC00029, 2 more genes
    nsv4865707copy number variation1nstd200human GRCh37 chr20: 61,679,033-61,760,916 , GRCh38.p12 chr20: 63,047,681-63,129,564 HAR1B, LOC105372719, 4 more genes
    nsv4862446copy number variation1nstd200human GRCh37 chr20: 61,666,477-61,677,141 , GRCh38.p12 chr20: 63,035,125-63,045,789 LINC01749, LINC00029, 1 more genes
    nsv4768191insertion1nstd199human GRCh37 chr20: 61,680,445-61,680,445 , GRCh38.p12 chr20: 63,049,093-63,049,093 LINC01749, LINC01056
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