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Items: 1 to 20 of 126

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148267copy number variation1nstd102humanPathogenic GRCh38 chr20: 87,153-23,635,465 , GRCh37.p13 chr20: 67,794-23,616,102 KRT18P3, RSPO4, 413 more genes
    nsv7037544copy number variation1nstd229human GRCh38 chr20: 10,055,782-10,059,711 , GRCh37.p13 chr20: 10,036,430-10,040,359 ANKEF1, SNAP25-AS1
    nsv7032788copy number variation1nstd229human GRCh38 chr20: 10,036,345-10,036,392 , GRCh37.p13 chr20: 10,016,993-10,017,040 ANKEF1, SNAP25-AS1
    nsv7028657copy number variation1nstd229human GRCh38 chr20: 9,741,351-10,201,152 , GRCh37.p13 chr20: 9,721,999-10,181,800 PAK5, ANKEF1, 3 more genes
    nsv7028615copy number variation1nstd229human GRCh38 chr20: 9,705,634-10,153,660 , GRCh37.p13 chr20: 9,686,282-10,134,308 ANKEF1, SNAP25-AS1, 2 more genes
    nsv7022729copy number variation1nstd229human GRCh38 chr20: 7,235,562-10,519,088 , GRCh37.p13 chr20: 7,216,209-10,499,736 MKKS, PHKBP1, 30 more genes
    nsv7022067copy number variation1nstd229human GRCh38 chr20: 7,868,752-11,491,709 , GRCh37.p13 chr20: 7,849,399-11,472,357 LOC339593, LOC105372522, 36 more genes
    nsv6528886copy number variation1nstd223human GRCh38 chr20: 10,027,101-10,037,100 , GRCh37.p13 chr20: 10,007,749-10,017,748 ANKEF1, SNAP25-AS1
    nsv6315526copy number variation1nstd102humanPathogenic GRCh37 chr20: 3,178,539-11,848,383 , GRCh38.p12 chr20: 3,197,893-11,867,735 LRRN4, MCM8-AS1, 129 more genes
    nsv6311245copy number variation1nstd102humanUncertain significance GRCh37 chr20: 7,812,350-10,654,278 , GRCh38.p12 chr20: 7,831,703-10,673,630 LOC100421490, RNU105B, 27 more genes
    nsv6133808copy number variation1nstd213human GRCh37 chr20: 3,300,000-12,130,001 , GRCh38.p12 chr20: 3,319,353-12,149,353 BMP2, CDC25B, 126 more genes
    nsv6111868insertion1nstd212human GRCh38 chr20: 10,034,917-10,034,917 , GRCh37.p13 chr20: 10,015,565-10,015,565 ANKEF1, SNAP25-AS1
    nsv5360044translocation1nstd200human GRCh38 chr20: 10,057,093-10,057,093 , GRCh38 chr20: 10,761,634-10,761,634 , GRCh37.p13 chr20: 10,037,741-10,037,741 , GRCh37.p13 chr20: 10,742,282-10,742,282 ANKEF1, SNAP25-AS1
    nsv5025122copy number variation1nstd200human GRCh38 chr20: 9,705,634-10,153,660 , GRCh37.p13 chr20: 9,686,282-10,134,308 SNAP25-AS1, PAK5, 2 more genes
    nsv4676419copy number variation1nstd102humanPathogenic GRCh37 chr20: 8,571,696-22,088,650 , GRCh38.p12 chr20: 8,591,049-22,108,012 PGAM3P, EEF1A1P34, 182 more genes
    nsv4349190copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,568-26,305,479 , GRCh38.p12 chr20: 80,927-26,324,843 LOC105372582, LOC101929937, 473 more genes
    nsv4336704sequence alteration1nstd166human GRCh37.p13 chr20: 8,105,854-23,795,733 , GRCh38.p12 chr20: 8,125,207-23,815,096 , BFSP1, 242 more genes
    nsv3923490copy number variation1nstd102humanPathogenic GRCh38 chr20: 80,106-13,029,401 , NCBI36 chr20: 8,747-12,958,049 , GRCh37 chr20: 60,747-13,010,049 LINC01751, RNA5SP474, 238 more genes
    nsv3922272copy number variation1nstd102humanPathogenic GRCh38 chr20: 80,106-30,227,427 , NCBI36 chr20: 8,747-28,075,764 , GRCh37 chr20: 60,747-29,462,103 ISM1-AS1, CST2, 498 more genes
    nsv3922170copy number variation1nstd102humanPathogenic NCBI36 chr20: 9,479,622-12,012,082 , GRCh38 chr20: 9,550,975-12,083,434 , GRCh37 chr20: 9,531,622-12,064,082 LOC107985384, PGAM3P, 32 more genes
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