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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
    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
    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
    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
    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
    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
    nsv4676332copy number variation1nstd102humanPathogenic GRCh37 chr20: 55,743,522-62,032,989 , GRCh38.p12 chr20: 57,168,466-63,401,636 BMP7, MIR298, 153 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
    nsv4457810copy number variation1nstd102humanUncertain significance GRCh37 chr20: 60,946,209-61,975,606 , GRCh38.p12 chr20: 62,371,153-63,344,254 SLCO4A1-AS2, ARFGAP1, 51 more genes
    nsv4436326complex substitution1nstd102humanUncertain significance GRCh37 chr20: 60,885,242-61,929,348 , GRCh38.p12 chr20: 62,310,186-63,297,996 COL9A3, LAMA5, 52 more genes
    nsv4357849copy number variation1nstd102humanPathogenic GRCh37 chr20: 54,143,747-62,194,881 , GRCh38.p12 chr20: 55,568,689-63,563,528 RBM38, LAMA5, 192 more genes
    nsv4289088copy number variation1nstd166human GRCh37.p13 chr20: 61,666,459-61,677,141 , GRCh38.p12 chr20: 63,035,107-63,045,789 LINC01056, LINC01749, 1 more genes
    nsv4273146copy number variation1nstd166human GRCh37.p13 chr20: 61,667,411-61,667,758 , GRCh38.p12 chr20: 63,036,059-63,036,406 LINC01056, LINC01749, 1 more genes
    nsv3966904insertion1nstd168human GRCh37.p13 chr20: 61,660,072-61,817,890 , GRCh38 chr20: 63,028,720-63,186,538 LINC01749, MIR124-3, 6 more genes
    nsv3966052copy number variation1nstd168human GRCh38 chr20: 62,990,639-63,071,212 , GRCh37.p13 chr20: 61,621,991-61,702,564 BHLHE23, LINC01056, 3 more genes
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