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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5940562copy number variation1nstd209human GRCh38 chr19: 10,087,983-10,088,286 , GRCh37.p13 chr19: 10,198,659-10,198,962 SHFL
    nsv5597256copy number variation1nstd207human GRCh38 chr19: 10,087,983-10,088,286 , GRCh37.p13 chr19: 10,198,659-10,198,962 SHFL
    nsv5532661copy number variation1nstd206human GRCh38 chr19: 10,083,639-10,084,914 , GRCh37.p13 chr19: 10,194,315-10,195,590 SHFL
    nsv5530645copy number variation1nstd206human GRCh38 chr19: 10,087,963-10,088,307 , GRCh37.p13 chr19: 10,198,639-10,198,983 SHFL
    nsv5284255copy number variation1nstd204human GRCh38.p13 chr19: 10,061,101-10,331,300 , GRCh37.p13 chr19: 10,171,777-10,441,976 ICAM1, ICAM4, 19 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
    nsv4630096copy number variation1nstd183human GRCh37 chr19: 10,200,424-10,200,607 , GRCh38.p12 chr19: 10,089,748-10,089,931 SHFL
    nsv4375402copy number variation1nstd173human GRCh37 chr19: 9,970,367-10,250,655 , GRCh38.p12 chr19: 9,859,691-10,139,979 P2RY11, RDH8, 12 more genes
    nsv3923449copy number variation1nstd102humanUncertain significance NCBI36 chr19: 9,956,287-10,064,514 , GRCh37.p13 chr19: 10,095,287-10,203,514 , GRCh38.p12 chr19: 9,984,611-10,092,838 COL5A3, ANGPTL6, 4 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
    nsv3879018copy number variation1nstd102humanUncertain significance GRCh37 chr19: 10,132,458-10,230,550 , GRCh38.p12 chr19: 10,021,782-10,119,874 SNORD105B, P2RY11, 9 more genes
    nsv3538810copy number variation2nstd152human GRCh38 chr19: 10,087,983-10,088,287 , GRCh37.p13 chr19: 10,198,659-10,198,963 SHFL
    nsv3180643mobile element deletion1nstd152human GRCh38 chr19: 10,087,984-10,088,288 , GRCh37.p13 chr19: 10,198,660-10,198,964 SHFL
    nsv3166981copy number variation1nstd151human GRCh37 chr19: 10,124,112-10,421,621 , GRCh38.p12 chr19: 10,013,436-10,310,945 ANGPTL6, EIF3G, 20 more genes
    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
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