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Items: 1 to 20 of 36

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3877600copy number variation1nstd102humanBenign GRCh37 chr5: 34,929,106-34,943,496 , GRCh38.p12 chr5: 34,929,001-34,943,391 DNAJC21
    nsv3883296copy number variation1nstd102humanBenign GRCh37 chr5: 34,929,544-34,943,496 , GRCh38.p12 chr5: 34,929,439-34,943,391 DNAJC21
    nsv3877784copy number variation1nstd102humanBenign GRCh37 chr5: 34,927,091-34,930,049 , GRCh38.p12 chr5: 34,926,986-34,929,944 DNAJC21
    nsv7097531copy number variation1nstd102humanUncertain significance GRCh37 chr5: 34,929,925-34,954,819 , GRCh38.p12 chr5: 34,929,820-34,954,714 DNAJC21
    nsv6312102copy number variation1nstd102humanUncertain significance GRCh37 chr5: 34,929,925-34,941,308 , GRCh38.p12 chr5: 34,929,820-34,941,203 DNAJC21
    nsv6312103copy number variation1nstd102humanUncertain significance GRCh37 chr5: 34,944,952-34,954,819 , GRCh38.p12 chr5: 34,944,847-34,954,714 DNAJC21
    nsv6312101copy number variation1nstd102humanUncertain significance GRCh37 chr5: 34,929,925-34,939,134 , GRCh38.p12 chr5: 34,929,820-34,939,029 DNAJC21
    nsv3887330copy number variation1nstd102humanUncertain significance GRCh37 chr5: 34,925,121-34,937,384 , GRCh38.p12 chr5: 34,925,016-34,937,279 DNAJC21, BRIX1
    nsv3874409copy number variation1nstd102humanUncertain significance GRCh37 chr5: 34,945,903-35,060,803 , GRCh38.p12 chr5: 34,945,798-35,060,701 DNAJC21, AGXT2, 1 more genes
    nsv3889848copy number variation1nstd102humanPathogenic GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719 DNAJC21, 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 DNAJC21, LOC105374666, 399 more genes
    nsv3914100copy number variation1nstd102humanPathogenic NCBI36 chr5: 30,184,899-35,249,537 , GRCh38 chr5: 30,149,035-35,213,678 , GRCh37 chr5: 30,149,142-35,213,780 DNAJC21, GUSBP18, 61 more genes
    nsv3886374copy number variation1nstd102humanPathogenic GRCh37 chr5: 13,648-180,905,029 , GRCh38.p12 chr5: 13,648-181,478,028 DNAJC21, LOC105374618, 2499 more genes
    nsv3871533copy number variation1nstd102humanPathogenic GRCh37 chr5: 25,328-180,693,344 , GRCh38.p12 chr5: 25,329-181,266,343 DNAJC21, PCDHGC5, 2492 more genes
    nsv3875235copy number variation2nstd102humanPathogenic GRCh37 chr5: 113,577-180,719,789 , GRCh38.p12 chr5: 113,462-181,292,788 DNAJC21, SPEF2, 2490 more genes
    nsv3911585copy number variation1nstd102humanPathogenic NCBI36 chr5: 75,149-73,744,306 , GRCh38 chr5: 22,149-74,412,725 , GRCh37 chr5: 22,149-73,708,550 DNAJC21, LINC02241, 878 more genes
    nsv3923992copy number variation1nstd102humanPathogenic GRCh37 chr5: 50,093-46,115,086 , NCBI36 chr5: 103,093-46,150,843 , GRCh38 chr5: 49,978-46,114,984 DNAJC21, LOC100130748, 533 more genes
    nsv3911295copy number variation1nstd102humanPathogenic GRCh37 chr5: 54,954-45,649,963 , NCBI36 chr5: 107,954-45,685,720 , GRCh38 chr5: 54,839-45,649,861 DNAJC21, PMCHL1, 532 more genes
    nsv3922539copy number variation1nstd102humanPathogenic NCBI36 chr5: 107,954-35,716,704 , GRCh37 chr5: 54,954-35,680,947 , GRCh38 chr5: 54,839-35,680,845 DNAJC21, MTCYBP37, 398 more genes
    nsv3889403copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,576-35,739,404 , GRCh38.p12 chr5: 113,461-35,739,302 DNAJC21, LOC101929003, 397 more genes
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