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Items: 1 to 20 of 107

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5667352inversion1nstd207human GRCh38 chr19: 47,959,661-50,091,195 , GRCh37.p13 chr19: 48,462,918-50,594,452 , AP2A1, 145 more genes
    nsv5179103mobile element insertion1nstd203human GRCh38 chr19: 49,675,260-49,675,274 , GRCh37.p13 chr19: 50,178,517-50,178,531 PRMT1
    nsv4729755copy number variation1nstd102humanPathogenic GRCh37 chr19: 48,463,931-57,095,254 , GRCh38.p12 chr19: 47,960,674-56,583,886 SIGLEC5, MED25, 574 more genes
    nsv4685764copy number variation1nstd102humannot provided GRCh37 chr19: 47,939,842-54,626,871 , GRCh38.p12 chr19: 47,436,585-54,071,460 SNAR-G1, IRF3, 453 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
    nsv4672450copy number variation1nstd186human GRCh37 chr19: 50,179,971-50,180,451 , GRCh38.p12 chr19: 49,676,714-49,677,194 PRMT1
    nsv4666246copy number variation2nstd186human GRCh37 chr19: 50,186,996-50,187,055 , GRCh38.p12 chr19: 49,683,739-49,683,798 PRMT1
    nsv4629758copy number variation1nstd183human GRCh37 chr19: 50,180,318-50,183,635 , GRCh38.p12 chr19: 49,677,061-49,680,378 PRMT1, MIR5088
    nsv4626069copy number variation2nstd183human GRCh37 chr19: 50,179,971-50,180,451 , GRCh38.p12 chr19: 49,676,714-49,677,194 PRMT1
    nsv4624857copy number variation1nstd183human GRCh37 chr19: 50,182,950-50,183,673 , GRCh38.p12 chr19: 49,679,693-49,680,416 MIR5088, PRMT1
    nsv4624844copy number variation1nstd183human GRCh37 chr19: 50,182,950-50,183,290 , GRCh38.p12 chr19: 49,679,693-49,680,033 PRMT1
    nsv4624742copy number variation2nstd183human GRCh37 chr19: 50,186,996-50,187,055 , GRCh38.p12 chr19: 49,683,739-49,683,798 PRMT1
    nsv4624524copy number variation1nstd183human GRCh37 chr19: 50,182,748-50,183,673 , GRCh38.p12 chr19: 49,679,491-49,680,416 PRMT1, MIR5088
    nsv4457465copy number variation1nstd102humanUncertain significance GRCh37 chr19: 49,600,909-51,366,070 , GRCh38.p12 chr19: 49,097,652-50,862,814 MED25, EMC10, 117 more genes
    nsv4376838copy number variation1nstd173human GRCh37 chr19: 48,462,617-51,107,899 , GRCh38.p12 chr19: 47,959,360-50,604,642 , LIN7B, 173 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
    nsv4271228copy number variation1nstd166human GRCh37.p13 chr19: 50,180,804-50,200,250 , GRCh38.p12 chr19: 49,677,547-49,696,993 PRMT1, ADM5, 2 more genes
    nsv4260702copy number variation1nstd166human GRCh37.p13 chr19: 50,182,000-50,198,000 , GRCh38.p12 chr19: 49,678,743-49,694,743 ADM5, CPT1C, 2 more genes
    nsv3919076copy number variation1nstd102humanPathogenic GRCh37 chr19: 48,432,832-59,083,573 , NCBI36 chr19: 53,124,644-63,775,385 , GRCh38 chr19: 47,929,575-58,572,206 KCNA7, ZNF28, 697 more genes
    nsv3911950copy number variation1nstd102humanPathogenic GRCh37 chr19: 48,411,797-59,051,332 , NCBI36 chr19: 53,103,609-63,743,144 , GRCh38 chr19: 47,908,540-58,539,965 LOC107987270, MIR6799, 694 more genes
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