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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3909326copy number variation1nstd102humanBenign GRCh37 chr10: 3,127,127-3,127,437 , GRCh38.p12 chr10: 3,084,935-3,085,245 PFKP
    nsv3909077copy number variation1nstd102humanBenign GRCh37 chr10: 3,079,772-3,151,325 , GRCh38.p12 chr10: 3,037,580-3,109,133 PFKP, PFKP-DT
    nsv3901356copy number variation1nstd102humanBenign GRCh37 chr10: 3,100,437-3,134,681 , GRCh38.p12 chr10: 3,058,245-3,092,489 PFKP, PFKP-DT
    nsv3916385copy number variation1nstd102humanLikely benign NCBI36 chr10: 2,710,973-3,090,958 , GRCh37 chr10: 2,720,973-3,100,958 , GRCh38 chr10: 2,678,781-3,058,766 LOC105376352, PFKP-DT
    nsv3923107copy number variation1nstd102humanBenign GRCh37 chr10: 3,148,116-3,202,491 , GRCh38 chr10: 3,105,924-3,160,299 PFKP, PITRM1, 2 more genes
    nsv3891836copy number variation1nstd102humanLikely benign GRCh37 chr10: 2,624,724-3,177,112 , GRCh38.p12 chr10: 2,582,532-3,134,920 PFKP, SNORD142, 3 more genes
    nsv3903375copy number variation1nstd102humanBenign GRCh37 chr10: 2,691,576-3,134,083 , GRCh38.p12 chr10: 2,649,384-3,091,891 PFKP, LOC105376352, 1 more genes
    nsv3901454copy number variation1nstd102humanBenign GRCh37 chr10: 2,695,158-3,134,083 , GRCh38.p12 chr10: 2,652,966-3,091,891 PFKP, LOC105376352, 1 more genes
    nsv3907893copy number variation1nstd102humanBenign GRCh37 chr10: 2,691,576-3,129,472 , GRCh38.p12 chr10: 2,649,384-3,087,280 PFKP, PFKP-DT, 1 more genes
    nsv3900366copy number variation1nstd102humanBenign GRCh37 chr10: 2,691,576-3,124,516 , GRCh38.p12 chr10: 2,649,384-3,082,324 PFKP, LOC105376352, 1 more genes
    nsv3912977copy number variation1nstd102humanBenign NCBI36 chr10: 2,685,392-3,114,061 , GRCh38 chr10: 2,653,200-3,081,869 , GRCh37 chr10: 2,695,392-3,124,061 PFKP, LOC105376352, 1 more genes
    nsv3905638copy number variation1nstd102humanBenign GRCh37 chr10: 2,819,465-3,111,473 , GRCh38.p12 chr10: 2,777,273-3,069,281 PFKP, PFKP-DT, 1 more genes
    nsv4456319copy number variation1nstd102humanUncertain significance GRCh37 chr10: 3,173,336-3,232,117 , GRCh38.p12 chr10: 3,131,144-3,189,925 PFKP, SNORD142, 2 more genes
    nsv3914736copy number variation1nstd102humanUncertain significance NCBI36 chr10: 2,363,294-3,090,934 , GRCh38 chr10: 2,331,100-3,058,742 , GRCh37 chr10: 2,373,294-3,100,934 LINC02645, LOC105376350, 3 more genes
    nsv3914771copy number variation1nstd102humanPathogenic GRCh38 chr10: 54,086-19,336,980 , NCBI36 chr10: 90,026-19,665,915 , GRCh37 chr10: 100,026-19,625,909 PFKP, COX6CP17, 302 more genes
    nsv3918372copy number variation1nstd102humanPathogenic GRCh38 chr10: 70,478-13,736,564 , GRCh37 chr10: 224,406-13,778,564 , NCBI36 chr10: 106,418-13,818,570 PFKP, IL9RP2, 232 more genes
    nsv3890577copy number variation1nstd102humanPathogenic GRCh37 chr10: 100,026-12,842,179 , GRCh38.p12 chr10: 54,086-12,800,180 PFKP, LOC105376364, 208 more genes
    nsv3893746copy number variation1nstd102humanPathogenic GRCh37 chr10: 136,361-8,850,609 , GRCh38.p12 chr10: 90,421-8,808,646 PFKP, TRV-TAC3-1, 163 more genes
    nsv5672604copy number variation1nstd102humanPathogenic GRCh37 chr10: 120,001-6,920,000 , GRCh38.p12 chr10: 74,061-6,878,038 PFKP, PITRM1-AS1, 133 more genes
    nsv3924022copy number variation1nstd102humanPathogenic NCBI36 chr10: 105,200-6,291,337 , GRCh38 chr10: 69,260-6,209,368 , GRCh37 chr10: 224,406-6,251,331 PFKP, LINC02561, 120 more genes
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