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Items: 1 to 20 of 152

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5927658copy number variation1nstd209human GRCh38 chr19: 38,876,987-38,877,576 , GRCh37.p13 chr19: 39,367,627-39,368,216 RINL, SIRT2
    nsv5530552copy number variation1nstd206human GRCh38 chr19: 38,872,442-38,875,666 , GRCh37.p13 chr19: 39,363,082-39,366,306 RINL
    nsv5292640copy number variation1nstd204human GRCh38.p13 chr19: 38,870,648-38,884,426 , GRCh37.p13 chr19: 39,361,288-39,375,066 RINL, SIRT2
    nsv5175478mobile element insertion1nstd203human GRCh38 chr19: 38,867,948-38,867,963 , GRCh37.p13 chr19: 39,358,588-39,358,603 RINL
    nsv4865161copy number variation1nstd200human GRCh37 chr19: 39,365,469-39,381,144 , GRCh38.p12 chr19|NW_014040929.1: 284,501-300,176 , GRCh38.p12 chr19: 38,874,829-38,890,504 SIRT2, RINL
    nsv4514643mobile element insertion1nstd166human GRCh37.p13 chr19: 39,366,678-39,366,678 , GRCh38.p12 chr19|NW_014040929.1: 285,710-285,710 , GRCh38.p12 chr19: 38,876,038-38,876,038 RINL
    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
    nsv4252989copy number variation1nstd166human GRCh37.p13 chr19: 39,350,427-39,373,599 , GRCh38.p12 chr19|NW_014040929.1: 269,459-292,631 , GRCh38.p12 chr19: 38,859,787-38,882,959 SIRT2, RINL
    nsv3913730copy number variation1nstd102humanPathogenic NCBI36 chr19: 11,199,618-49,821,491 , GRCh37 chr19: 11,338,618-45,129,651 , GRCh38 chr19: 11,227,942-44,626,354 BCKDHA, ADGRE5, 1102 more genes
    nsv3912447copy number variation1nstd102humanPathogenic NCBI36 chr19: 42,502,119-47,934,680 , GRCh37 chr19: 37,810,279-43,242,840 , GRCh38 chr19: 37,319,377-42,738,688 MIR8077, TRI-TAT1-1, 233 more genes
    nsv3912394copy number variation1nstd102humanUncertain significance NCBI36 chr19: 44,054,509-44,534,649 , GRCh37.p13 chr19: 39,362,669-39,842,809 , GRCh38.p12 chr19: 38,872,029-39,352,169 SAMD4B, IFNL1, 20 more genes
    nsv3906103copy number variation1nstd102humanUncertain significance GRCh37 chr19: 39,360,343-39,369,195 , GRCh38.p12 chr19|NW_014040929.1: 279,375-288,227 , GRCh38.p12 chr19: 38,869,703-38,878,555 SIRT2, RINL
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 ZNF321P, ZNF861P, 2443 more genes
    nsv3903203copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793 BABAM1, BEST2, 2426 more genes
    nsv3903092copy number variation2nstd102humanPathogenic GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521 LENG8, SYDE1, 2408 more genes
    nsv3895066copy number variation1nstd102humanPathogenic GRCh37 chr19: 37,582,250-41,630,908 , GRCh38.p12 chr19: 37,091,348-41,125,003 RNU6-140P, COQ8B, 162 more genes
    nsv3169031copy number variation1nstd158human GRCh38.p12 chr19: 38,412,977-41,901,266 , GRCh37 chr19: 38,903,617-42,405,416 , ACTN4, 162 more genes
    nsv3168446copy number variation1nstd158human GRCh37 chr19: 35,445,908-45,506,757 , GRCh38.p12 chr19: 34,955,004-45,003,499 , ACTN4, 449 more genes
    nsv3163170copy number variation14nstd151human GRCh37 chr19: 39,359,741-39,372,136 , GRCh38.p12 chr19|NW_014040929.1: 278,773-291,168 , GRCh38.p12 chr19: 38,869,101-38,881,496 RINL, SIRT2
    nsv3160366copy number variation2nstd151human GRCh37 chr19: 39,359,741-39,371,800 , GRCh38.p12 chr19|NW_014040929.1: 278,773-290,832 , GRCh38.p12 chr19: 38,869,101-38,881,160 SIRT2, RINL
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