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Items: 1 to 20 of 105

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3886476copy number variation1nstd102humanBenign GRCh37 chr5: 10,636,151-10,650,324 , GRCh38.p12 chr5: 10,636,039-10,650,212 ANKRD33B
    nsv3877377copy number variation1nstd102humanBenign GRCh37 chr5: 10,638,180-10,650,040 , GRCh38.p12 chr5: 10,638,068-10,649,928 ANKRD33B
    nsv3884221copy number variation1nstd102humanBenign GRCh37 chr5: 10,639,138-10,650,324 , GRCh38.p12 chr5: 10,639,026-10,650,212 ANKRD33B
    nsv3876674copy number variation1nstd102humanBenign GRCh37 chr5: 10,639,295-10,650,324 , GRCh38.p12 chr5: 10,639,183-10,650,212 ANKRD33B
    nsv3871838copy number variation1nstd102humanBenign GRCh37 chr5: 10,639,138-10,650,146 , GRCh38.p12 chr5: 10,639,026-10,650,034 ANKRD33B
    nsv3871439copy number variation1nstd102humanBenign GRCh37 chr5: 10,639,138-10,650,040 , GRCh38.p12 chr5: 10,639,026-10,649,928 ANKRD33B
    nsv3878663copy number variation1nstd102humanBenign GRCh37 chr5: 10,639,138-10,649,378 , GRCh38.p12 chr5: 10,639,026-10,649,266 ANKRD33B
    nsv3879910copy number variation1nstd102humanBenign GRCh37 chr5: 10,562,901-10,565,088 , GRCh38.p12 chr5: 10,562,789-10,564,976 ANKRD33B
    nsv3874886copy number variation1nstd102humanBenign GRCh37 chr5: 10,649,729-10,650,324 , GRCh38.p12 chr5: 10,649,617-10,650,212 ANKRD33B
    nsv3914649copy number variation1nstd102humanPathogenic GRCh38 chr5: 22,149-35,831,538 , GRCh37 chr5: 22,149-35,831,640 , NCBI36 chr5: 75,149-35,867,397 ANKRD33B, LOC105374666, 399 more genes
    nsv3887142copy number variation1nstd102humanPathogenic GRCh37 chr5: 22,149-34,041,196 , GRCh38.p12 chr5: 22,149-34,041,091 ANKRD33B, H3Y1, 381 more genes
    nsv3910712copy number variation1nstd102humanPathogenic NCBI36 chr5: 166,576-34,034,151 , GRCh38 chr5: 113,461-33,998,289 , GRCh37 chr5: 113,576-33,998,394 ANKRD33B, ROPN1L, 378 more genes
    nsv3924496copy number variation1nstd102humanPathogenic GRCh37 chr5: 22,149-32,248,116 , NCBI36 chr5: 75,149-32,283,873 , GRCh38 chr5: 22,149-32,248,010 ANKRD33B, LOC105374678, 356 more genes
    nsv6636942copy number variation1nstd102humanPathogenic GRCh37 chr5: 1-32,091,038 , GRCh38.p12 chr5: 10,001-32,090,932 ANKRD33B, LOC105374608, 351 more genes
    nsv6636606copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,577-31,448,527 , GRCh38.p12 chr5: 113,462-31,448,420 ANKRD33B, BASP1, 338 more genes
    nsv3881706copy number variation1nstd102humanPathogenic GRCh37 chr5: 25,328-31,343,671 , GRCh38.p12 chr5: 25,329-31,343,564 ANKRD33B, IRX2-DT, 339 more genes
    nsv3883796copy number variation1nstd102humanPathogenic GRCh37 chr5: 25,328-30,672,798 , GRCh38.p12 chr5: 25,329-30,672,691 ANKRD33B, H3P22, 335 more genes
    nsv6315416copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,576-30,712,376 , GRCh38.p12 chr5: 113,461-30,712,269 ANKRD33B, LOC105374649, 333 more genes
    nsv3912696copy number variation1nstd102humanPathogenic GRCh37 chr5: 50,093-30,112,642 , GRCh38 chr5: 49,978-30,112,535 , NCBI36 chr5: 103,093-30,148,399 ANKRD33B, OTULINL, 333 more genes
    nsv5381771copy number variation1nstd102humanPathogenic GRCh37 chr5: 22,149-29,048,823 , GRCh38.p12 chr5: 22,149-29,048,716 ANKRD33B, OTULINL, 317 more genes
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