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Items: 1 to 20 of 259

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5695842mobile element insertion1nstd211human GRCh38 chr13: 95,594,946-95,594,946 , GRCh37.p13 chr13: 96,247,200-96,247,200 DZIP1
    nsv5672807copy number variation1nstd102humanPathogenic GRCh37 chr13: 92,002,837-103,343,314 , GRCh38.p12 chr13: 91,350,583-102,690,964 RPL7L1P12, MIR548AS, 153 more genes
    nsv5672796copy number variation1nstd102humanPathogenic GRCh37 chr13: 94,679,977-111,536,145 , GRCh38.p12 chr13: 94,027,723-110,883,798 LINC00359, LOC107984609, 220 more genes
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 RN7SL272P, DIAPH3, 1333 more genes
    nsv5431089mobile element insertion1nstd206human GRCh38 chr13: 95,594,946-95,594,997 , GRCh37.p13 chr13: 96,247,200-96,247,251 DZIP1
    nsv5192638mobile element insertion1nstd203human GRCh38 chr13: 95,642,502-95,642,512 , GRCh37.p13 chr13: 96,294,756-96,294,766 DZIP1
    nsv5033445inversion1nstd200human GRCh38 chr13: 63,639,797-112,722,344 , GRCh37.p13 chr13: 64,213,930-113,376,658 , RPL15P18, 564 more genes
    nsv4998252copy number variation1nstd200human GRCh38 chr13: 95,587,991-95,593,681 , GRCh37.p13 chr13: 96,240,245-96,245,935 DZIP1
    nsv4998251copy number variation1nstd200human GRCh38 chr13: 95,580,516-95,582,929 , GRCh37.p13 chr13: 96,232,770-96,235,183 DZIP1
    nsv4871044inversion1nstd200human GRCh37 chr13: 64,213,930-113,376,658 , GRCh38.p12 chr13: 63,639,797-112,722,344 , TUBGCP3, 564 more genes
    nsv4844999copy number variation1nstd200human GRCh37 chr13: 96,234,640-96,271,660 , GRCh38.p12 chr13: 95,582,386-95,619,406 DZIP1
    nsv4729508copy number variation1nstd102humanUncertain significance GRCh37 chr13: 96,225,567-96,456,089 , GRCh38.p12 chr13: 95,573,313-95,803,835 MTCYBP3, DZIP1, 6 more genes
    nsv4714910copy number variation1nstd195human GRCh37 chr13: 96,219,951-96,342,351 , GRCh38.p12 chr13: 95,567,697-95,690,097 DNAJC3, CLDN10, 2 more genes
    nsv4676071copy number variation1nstd102humanUncertain significance GRCh37 chr13: 94,896,219-96,993,668 , GRCh38.p12 chr13: 94,243,965-96,341,414 SNORD13G, LINC00557, 33 more genes
    nsv4675892copy number variation1nstd102humanPathogenic GRCh37 chr13: 96,240,346-106,103,782 , GRCh38.p12 chr13: 95,588,092-105,451,433 LOC105370328, LINC00554, 132 more genes
    nsv4675850copy number variation1nstd102humanPathogenic GRCh37 chr13: 53,262,013-115,107,733 , GRCh38.p12 chr13: 52,687,878-114,342,258 TEX30, LOC101927712, 680 more genes
    nsv4569381mobile element insertion1nstd166human GRCh37.p13 chr13: 96,260,590-96,260,590 , GRCh38.p12 chr13: 95,608,336-95,608,336 DZIP1
    nsv4529543copy number variation1nstd166human GRCh37.p13 chr13: 96,261,001-96,261,329 , GRCh38.p12 chr13: 95,608,747-95,609,075 DZIP1
    nsv4511321mobile element insertion1nstd166human GRCh37.p13 chr13: 96,257,625-96,257,625 , GRCh38.p12 chr13: 95,605,371-95,605,371 DZIP1
    nsv4507581mobile element insertion1nstd166human GRCh37.p13 chr13: 96,238,188-96,238,188 , GRCh38.p12 chr13: 95,585,934-95,585,934 DZIP1
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