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Items: 1 to 20 of 82

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5937899copy number variation1nstd209human GRCh38 chr19: 9,845,252-9,845,376 , GRCh37.p13 chr19: 9,955,928-9,956,052 PIN1
    nsv5011567copy number variation1nstd200human GRCh38 chr19: 9,836,771-9,836,904 , GRCh37.p13 chr19: 9,947,447-9,947,580 PIN1
    nsv4729799copy number variation1nstd102humanUncertain significance GRCh37 chr19: 8,518,395-10,053,298 , GRCh38.p12 chr19: 8,453,511-9,942,622 ZNF426-DT, ADAMTS10, 61 more genes
    nsv4679505copy number variation1nstd189human GRCh37.p13 chr19: 9,903,732-10,322,986 , GRCh38.p12 chr19: 9,793,056-10,212,310 DNMT1, P2RY11, 18 more genes
    nsv4436244complex substitution1nstd102humanUncertain significance GRCh38.p12 chr19: 8,891,157-9,974,378 , GRCh37 chr19: 9,001,833-10,085,054 PIN1, UBE2L4, 51 more genes
    nsv4255437copy number variation1nstd166human GRCh37.p13 chr19: 9,941,000-9,948,000 , GRCh38.p12 chr19: 9,830,324-9,837,324 PIN1, UBL5, 1 more genes
    nsv4252481copy number variation1nstd166human GRCh37.p13 chr19: 9,947,447-9,947,580 , GRCh38.p12 chr19: 9,836,771-9,836,904 PIN1
    nsv3960084copy number variation1nstd168human GRCh38 chr19: 9,808,861-9,847,406 , GRCh37.p13 chr19: 9,919,537-9,958,082 PIN1, UBL5, 3 more genes
    nsv3920616copy number variation1nstd102humanLikely pathogenic NCBI36 chr19: 8,802,823-13,303,041 , GRCh37 chr19: 8,941,823-13,442,041 , GRCh38 chr19: 8,831,147-13,331,227 ACP5, GET3, 236 more genes
    nsv3912242copy number variation1nstd102humanPathogenic GRCh37 chr19: 9,846,119-11,338,677 , GRCh38 chr19: 9,735,443-11,228,001 , NCBI36 chr19: 9,707,119-11,199,677 PPAN, S1PR5, 68 more genes
    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
    nsv3898900copy number variation1nstd102humanPathogenic GRCh37 chr19: 9,678,768-14,853,426 , GRCh38.p12 chr19: 9,568,092-14,742,614 FBXL12, DCAF15, 253 more genes
    nsv3888397copy number variation1nstd102humanLikely pathogenic GRCh38 chr19: 7,981,357-10,019,383 , GRCh37.p13 chr19: 8,046,241-10,130,059 ELAVL1, MYO1F, 80 more genes
    nsv3223715copy number variation1nstd152human GRCh38 chr19: 9,845,237-9,845,392 , GRCh37.p13 chr19: 9,955,913-9,956,068 PIN1
    nsv2768220copy-neutral loss of heterozygosity1nstd125human GRCh38.p12 chr19: 5,092,438-17,933,476 , GRCh37 chr19: 5,092,449-18,044,285 , ACP5, 562 more genes
    nsv2768219copy-neutral loss of heterozygosity1nstd125human GRCh38.p12 chr19: 260,911-20,692,745 , GRCh37 chr19: 260,911-20,875,551 , ACP5, 914 more genes
    nsv2768218copy-neutral loss of heterozygosity1nstd125human GRCh38.p12 chr19: 260,911-19,745,645 , GRCh37 chr19: 260,911-19,856,454 , ACP5, 867 more genes
    nsv2768217copy-neutral loss of heterozygosity1nstd125human GRCh38.p12 chr19: 260,911-16,062,156 , GRCh37 chr19: 260,911-16,172,966 , ACP5, 724 more genes
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