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Items: 1 to 20 of 99

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5699359mobile element insertion1nstd211human GRCh38 chr19: 46,619,550-46,619,550 , GRCh37.p13 chr19: 47,122,807-47,122,807 PTGIR
    nsv5697551mobile element insertion1nstd211human GRCh38 chr19: 46,619,669-46,619,669 , GRCh37.p13 chr19: 47,122,926-47,122,926 PTGIR
    nsv5327184copy number variation1nstd204human GRCh37.p13 chr19: 47,121,445-47,145,672 , GRCh38.p13 chr19: 46,618,188-46,642,415 PTGIR, GNG8
    nsv5289378copy number variation1nstd204human GRCh38.p13 chr19: 46,618,275-46,637,823 , GRCh37.p13 chr19: 47,121,532-47,141,080 PTGIR, GNG8
    nsv5287619copy number variation1nstd204human GRCh38.p13 chr19: 46,623,979-46,625,714 , GRCh37.p13 chr19: 47,127,236-47,128,971 PTGIR
    nsv5168833mobile element insertion1nstd203human GRCh38 chr19: 46,618,014-46,618,032 , GRCh37.p13 chr19: 47,121,271-47,121,289 PTGIR
    nsv5020772copy number variation1nstd200human GRCh38 chr19: 46,618,197-46,642,406 , GRCh37.p13 chr19: 47,121,454-47,145,663 PTGIR, GNG8
    nsv4853137copy number variation1nstd200human GRCh37 chr19: 47,121,454-47,145,663 , GRCh38.p12 chr19: 46,618,197-46,642,406 GNG8, PTGIR
    nsv4682791copy number variation1nstd102humanUncertain significance GRCh37 chr19: 47,109,074-47,260,205 , GRCh38.p12 chr19: 46,605,817-46,756,948 DACT3, FKRP, 9 more genes
    nsv4676357copy number variation1nstd102humanPathogenic GRCh37 chr19: 44,738,088-53,621,561 , GRCh38.p12 chr19: 44,233,935-53,118,308 MIR4324, KLK9, 485 more genes
    nsv4676350copy number variation1nstd102humanUncertain significance GRCh37 chr19: 45,531,056-48,174,177 , GRCh38.p12 chr19: 45,027,798-47,670,920 NKPD1, IGFL1, 112 more genes
    nsv4457372copy number variation1nstd102humanPathogenic GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575 ZNF461, LOC101927572, 735 more genes
    nsv4350827copy number variation1nstd102humanPathogenic GRCh37 chr19: 47,036,361-48,525,536 , GRCh38.p12 chr19: 46,533,104-48,022,279 LINC01595, SNAR-A13, 59 more genes
    nsv4321864inversion1nstd166human GRCh37.p13 chr19: 46,657,897-51,634,775 , GRCh38.p12 chr19: 46,154,640-51,131,518 , C5AR1, 288 more genes
    nsv4261305copy number variation1nstd166human GRCh37.p13 chr19: 47,122,770-47,122,849 , GRCh38.p12 chr19: 46,619,513-46,619,592 PTGIR
    nsv4253086copy number variation1nstd166human GRCh37.p13 chr19: 47,116,305-47,116,782 , GRCh38.p12 chr19: 46,613,048-46,613,525 PTGIR
    nsv3961146insertion1nstd168human GRCh38 chr19: 46,611,784-46,614,331 , GRCh37.p13 chr19: 47,115,041-47,117,588 PTGIR
    nsv3956484insertion1nstd168human GRCh38 chr19: 46,602,113-46,610,877 , GRCh37.p13 chr19: 47,105,370-47,114,134 CALM3, PTGIR
    nsv3950467copy number variation1nstd167human GRCh37 chr19: 47,122,772-47,122,812 , GRCh38.p12 chr19: 46,619,515-46,619,555 PTGIR
    nsv3924836copy number variation1nstd102humanPathogenic NCBI36 chr19: 50,166,517-53,452,471 , GRCh37 chr19: 45,474,677-48,760,659 , GRCh38 chr19: 44,971,420-48,257,402 IGFL1P1, LOC105372426, 145 more genes
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