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Items: 1 to 20 of 197

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5969116insertion1nstd209human GRCh38 chr17: 4,668,881-4,668,881 , GRCh37.p13 chr17: 4,572,176-4,572,176 PELP1
    nsv5705973mobile element insertion1nstd211human GRCh38 chr17: 4,676,918-4,676,918 , GRCh37.p13 chr17: 4,580,213-4,580,213 PELP1
    nsv5528577copy number variation1nstd206human GRCh38 chr17: 4,683,487-4,683,798 , GRCh37.p13 chr17: 4,586,782-4,587,093 PELP1
    nsv5526629copy number variation1nstd206human GRCh38 chr17: 4,684,919-4,686,681 , GRCh37.p13 chr17: 4,588,214-4,589,976 PELP1
    nsv5414959mobile element insertion1nstd206human GRCh38 chr17: 4,676,918-4,676,969 , GRCh37.p13 chr17: 4,580,213-4,580,264 PELP1
    nsv5159201mobile element insertion1nstd203human GRCh38 chr17: 4,683,506-4,683,531 , GRCh37.p13 chr17: 4,586,801-4,586,826 PELP1
    nsv5154010mobile element insertion1nstd203human GRCh38 chr17: 4,683,510-4,683,548 , GRCh37.p13 chr17: 4,586,805-4,586,843 PELP1
    nsv5146801mobile element insertion1nstd203human GRCh38 chr17: 4,694,497-4,694,502 , GRCh37.p13 chr17: 4,597,792-4,597,797 PELP1
    nsv5145735mobile element insertion1nstd203human GRCh38 chr17: 4,683,531-4,683,548 , GRCh37.p13 chr17: 4,586,826-4,586,843 PELP1
    nsv5145186mobile element insertion1nstd203human GRCh38 chr17: 4,676,902-4,676,918 , GRCh37.p13 chr17: 4,580,197-4,580,213 PELP1
    nsv4857820copy number variation1nstd200human GRCh37 chr17: 4,586,790-4,588,231 , GRCh38.p12 chr17: 4,683,495-4,684,936 PELP1
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4675837copy number variation1nstd102humanUncertain significance GRCh37 chr17: 4,245,304-4,581,861 , GRCh38.p12 chr17: 4,342,009-4,678,566 TXNP4, SPNS3, 13 more genes
    nsv4674950copy number variation1nstd102humanUncertain significance GRCh37 chr17: 3,933,998-4,581,861 , GRCh38.p12 chr17: 4,030,704-4,678,566 UBE2G1, PELP1, 20 more genes
    nsv4674912copy number variation1nstd102humanPathogenic GRCh37 chr17: 8,547-5,627,408 , GRCh38.p12 chr17: 158,756-5,724,088 SRR, DBIL5P, 196 more genes
    nsv4630208copy number variation1nstd183human GRCh37 chr17: 4,486,568-5,620,052 , GRCh38.p12 chr17: 4,583,273-5,716,732 , ARRB2, 59 more genes
    nsv4577833mobile element insertion1nstd166human GRCh37.p13 chr17: 4,578,692-4,578,692 , GRCh38.p12 chr17: 4,675,397-4,675,397 PELP1
    nsv4506475mobile element insertion1nstd166human GRCh37.p13 chr17: 4,580,197-4,580,197 , GRCh38.p12 chr17: 4,676,902-4,676,902 PELP1
    nsv4457587copy number variation1nstd102humanUncertain significance GRCh37 chr17: 3,759,126-6,128,911 , GRCh38.p12 chr17: 3,855,832-6,225,591 DERL2, ZZEF1, 82 more genes
    nsv4350781copy number variation1nstd102humanPathogenic GRCh37 chr17: 47,546-6,287,620 , GRCh38.p12 chr17: 197,755-6,384,300 SERPINF1, UBE2G1, 201 more genes
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