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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3902887copy number variation1nstd102humanBenign GRCh37 chr16: 55,837,121-55,858,428 , GRCh38.p12 chr16: 55,803,209-55,824,516 CES1
    nsv3907590copy number variation1nstd102humanBenign GRCh37 chr16: 55,842,404-55,851,296 , GRCh38.p12 chr16: 55,808,492-55,817,384 CES1
    nsv3897687copy number variation1nstd102humanBenign GRCh37 chr16: 55,822,531-55,853,379 , GRCh38.p12 chr16: 55,788,619-55,819,467 CES1
    nsv3891351copy number variation1nstd102humanBenign GRCh37 chr16: 55,842,577-55,864,452 , GRCh38.p12 chr16: 55,808,665-55,830,540 CES1
    nsv3894158copy number variation1nstd102humanBenign GRCh37 chr16: 55,842,641-55,856,717 , GRCh38.p12 chr16: 55,808,729-55,822,805 CES1
    nsv3909307copy number variation1nstd102humanBenign GRCh37 chr16: 55,844,609-55,856,717 , GRCh38.p12 chr16: 55,810,697-55,822,805 CES1
    nsv3900898copy number variation1nstd102humanBenign GRCh37 chr16: 55,842,641-55,853,059 , GRCh38.p12 chr16: 55,808,729-55,819,147 CES1
    nsv4455622copy number variation1nstd102humanUncertain significance GRCh37 chr16: 55,837,726-55,863,303 , GRCh38.p12 chr16: 55,803,814-55,829,391 CES1
    nsv3895916copy number variation1nstd102humanBenign GRCh37 chr16: 55,795,214-55,842,641 , GRCh38.p12 chr16: 55,761,302-55,808,729 CES1, CES1P1
    nsv3893460copy number variation1nstd102humanBenign GRCh37 chr16: 55,799,230-55,842,641 , GRCh38.p12 chr16: 55,765,318-55,808,729 CES1P1, CES1
    nsv3891816copy number variation1nstd102humanBenign GRCh37 chr16: 55,800,809-55,842,641 , GRCh38.p12 chr16: 55,766,897-55,808,729 CES1, CES1P1
    nsv3890958copy number variation1nstd102humanLikely benign GRCh37 chr16: 66,975,093-67,039,211 , GRCh38.p12 chr16: 66,941,190-67,005,308 CES2, LOC107984881, 2 more genes
    nsv4457115copy number variation1nstd102humanUncertain significance GRCh37 chr16: 55,773,119-55,843,724 , GRCh38.p12 chr16: 55,739,207-55,809,812 CES1P1, CES1P2, 1 more genes
    nsv3918978copy number variation1nstd102humanUncertain significance GRCh38 chr16: 66,945,487-67,024,713 , NCBI36 chr16: 65,536,891-65,616,117 , GRCh37 chr16: 66,979,390-67,058,616 CES2, RN7SL543P, 3 more genes
    nsv3916542copy number variation1nstd102humanPathogenic GRCh38 chr16: 55,457,477-63,841,622 , NCBI36 chr16: 54,048,890-62,433,027 , GRCh37 chr16: 55,491,389-63,875,526 CES1, SNORA46, 139 more genes
    nsv3916762copy number variation1nstd102humanPathogenic GRCh37 chr16: 62,213,235-67,804,317 , GRCh38 chr16: 62,179,331-67,770,414 , NCBI36 chr16: 60,770,736-66,361,818 CES2, RANBP10, 87 more genes
    nsv4675201copy number variation1nstd102humanPathogenic GRCh37 chr16: 65,669,673-70,180,183 , GRCh38.p12 chr16: 65,635,770-70,146,280 CES2, LOC100420066, 143 more genes
    nsv6315060copy number variation1nstd102humanPathogenic GRCh38 chr16: 53,818,483-57,631,312 , GRCh37.p13 chr16: 53,852,395-57,665,224 LOC105371283, MT1A, 91 more genes
    nsv3910745copy number variation1nstd102humanPathogenic NCBI36 chr16: 62,902,680-66,653,415 , GRCh38 chr16: 64,311,275-68,062,011 , GRCh37 chr16: 64,345,179-68,095,914 CES2, PSMB10, 95 more genes
    nsv7094682copy number variation2nstd102humanPathogenic GRCh37 chr16: 65,821,800-67,208,957 , GRCh38.p12 chr16: 65,787,897-67,175,054 CES2, RNA5SP428, 38 more genes
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