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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3886576copy number variation1nstd102humanBenign GRCh37 chr5: 22,655,865-22,718,422 , GRCh38.p12 chr5: 22,655,756-22,718,313 CDH12
    nsv3881741copy number variation1nstd102humanBenign GRCh37 chr5: 22,812,264-22,866,518 , GRCh38.p12 chr5: 22,812,155-22,866,409 CDH12
    nsv3871119copy number variation1nstd102humanBenign GRCh37 chr5: 22,812,264-22,856,741 , GRCh38.p12 chr5: 22,812,155-22,856,632 CDH12
    nsv6637031copy number variation1nstd102humanUncertain significance GRCh37 chr5: 21,740,926-21,792,313 , GRCh38.p12 chr5: 21,740,817-21,792,204 CDH12
    nsv3877628copy number variation1nstd102humanBenign GRCh37 chr5: 22,156,155-22,233,716 , GRCh38.p12 chr5: 22,156,046-22,233,607 CDH12, LOC105374682
    nsv3879512copy number variation1nstd102humanUncertain significance GRCh37 chr5: 22,770,421-23,082,328 , GRCh38.p12 chr5: 22,770,312-23,082,219 CDH12, LOC105374686
    nsv3916081copy number variation1nstd102humanLikely benign NCBI36 chr5: 21,966,989-22,261,625 , GRCh37 chr5: 21,931,232-22,225,868 , GRCh38 chr5: 21,931,123-22,225,759 CDH12, LOC105374682, 2 more genes
    nsv3915624copy number variation1nstd102humanBenign NCBI36 chr5: 21,907,898-22,192,403 , GRCh37 chr5: 21,872,141-22,156,646 , GRCh38 chr5: 21,872,032-22,156,537 CDH12, PMCHL1, 3 more genes
    nsv4674363copy number variation1nstd102humanUncertain significance GRCh37 chr5: 22,284,859-22,762,721 , GRCh38.p12 chr5: 22,284,750-22,762,612 CDH12, GCNT1P2, 2 more genes
    nsv6636480copy number variation1nstd102humanUncertain significance GRCh37 chr5: 22,130,874-22,556,566 , GRCh38.p12 chr5: 22,130,765-22,556,457 CDH12, LOC105374682, 1 more genes
    nsv3924463copy number variation1nstd102humanUncertain significance NCBI36 chr5: 21,955,641-22,279,464 , GRCh38 chr5: 21,919,775-22,243,598 , GRCh37 chr5: 21,919,884-22,243,707 CDH12, PMCHL1, 2 more genes
    nsv3921111copy number variation1nstd102humanUncertain significance GRCh37 chr5: 21,852,834-21,964,183 , NCBI36 chr5: 21,888,591-21,999,940 , GRCh38 chr5: 21,852,725-21,964,074 CDH12, SNORA105A, 2 more genes
    nsv3878374copy number variation1nstd102humanUncertain significance GRCh37 chr5: 22,657,926-23,156,895 , GRCh38.p12 chr5: 22,657,817-23,156,786 CDH12, LOC105374686, 1 more genes
    nsv3920845copy number variation1nstd102humanUncertain significance GRCh38 chr5: 22,156,478-22,582,784 , NCBI36 chr5: 22,192,344-22,618,650 , GRCh37 chr5: 22,156,587-22,582,893 CDH12, LOC105374682, 2 more genes
    nsv4674642copy number variation1nstd102humanUncertain significance GRCh37 chr5: 21,528,584-21,845,788 , GRCh38.p12 chr5: 21,528,475-21,845,679 , GRCh38.p12 chr5|NW_016107297.1: 177,611-362,221 CDH12, GUSBP1, 2 more genes
    nsv3916680copy number variation1nstd102humanUncertain significance NCBI36 chr5: 22,600,157-22,850,091 , GRCh37.p13 chr5: 22,564,400-22,814,334 , GRCh38.p12 chr5: 22,564,291-22,814,225 CDH12, GCNT1P2, 2 more genes
    nsv3889848copy number variation1nstd102humanPathogenic GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719 CDH12, MEGF10, 2080 more genes
    nsv3914649copy number variation1nstd102humanPathogenic GRCh38 chr5: 22,149-35,831,538 , GRCh37 chr5: 22,149-35,831,640 , NCBI36 chr5: 75,149-35,867,397 CDH12, LOC105374666, 399 more genes
    nsv3887142copy number variation1nstd102humanPathogenic GRCh37 chr5: 22,149-34,041,196 , GRCh38.p12 chr5: 22,149-34,041,091 CDH12, 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 CDH12, ROPN1L, 378 more genes
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