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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4729324copy number variation1nstd102humanLikely benign GRCh37 chr10: 34,489,782-34,563,236 , GRCh38.p12 chr10: 34,200,854-34,274,308 PARD3
    nsv3899211copy number variation1nstd102humanBenign GRCh37 chr10: 34,754,684-34,774,914 , GRCh38.p12 chr10: 34,465,756-34,485,986 PARD3
    nsv4675504copy number variation1nstd102humanUncertain significance GRCh37 chr10: 34,974,284-35,055,950 , GRCh38.p12 chr10: 34,685,356-34,767,022 PARD3
    nsv4675568copy number variation1nstd102humanUncertain significance GRCh37 chr10: 34,821,897-34,888,936 , GRCh38.p12 chr10: 34,532,969-34,600,008 PARD3
    nsv3901610copy number variation1nstd102humanBenign/Likely benign GRCh37 chr10: 35,061,767-35,157,790 , GRCh38.p12 chr10: 34,772,839-34,868,862 PARD3, PARD3-DT
    nsv6637213copy number variation1nstd102humanUncertain significance GRCh37 chr10: 34,632,457-34,903,414 , GRCh38.p12 chr10: 34,343,529-34,614,486 ELOBP4, PARD3
    nsv4436774copy number variation1nstd102humanUncertain significance GRCh37 chr20: 32,837,318-32,927,360 , GRCh38.p12 chr20: 34,249,512-34,339,554 ASIP, AHCY
    nsv3876801copy number variation1nstd102humanPathogenic GRCh37 chr10: 34,835,589-34,975,192 , GRCh38 chr10: 34,546,661-34,686,264 PARD3, RPL37P18, 1 more genes
    nsv3972386copy number variation1nstd102humanLikely benign GRCh37 chr10: 34,885,187-35,165,071 , GRCh38.p12 chr10: 34,596,259-34,876,143 RPL37P18, SS18L2P1, 3 more genes
    nsv3924745copy number variation1nstd102humanBenign NCBI36 chr10: 35,095,364-35,223,407 , GRCh37 chr10: 35,055,358-35,183,401 , GRCh38 chr10: 34,766,430-34,894,473 PARD3, PARD3-DT, 1 more genes
    nsv3918233copy number variation1nstd102humanUncertain significance GRCh38 chr10: 34,149,753-34,733,161 , NCBI36 chr10: 34,478,687-35,062,095 , GRCh37 chr10: 34,438,681-35,022,089 RPL37P18, ELOBP4, 3 more genes
    nsv3919360copy number variation1nstd102humanUncertain significance NCBI36 chr10: 34,450,217-35,019,693 , GRCh37 chr10: 34,410,211-34,979,687 , GRCh38 chr10: 34,121,283-34,690,759 RPS12P16, PARD3, 3 more genes
    nsv3913776copy number variation1nstd102humanUncertain significance GRCh37 chr10: 34,527,993-34,944,192 , GRCh38 chr10: 34,239,065-34,655,264 , NCBI36 chr10: 34,567,999-34,984,198 ELOBP4, PARD3, 1 more genes
    nsv4675459copy number variation1nstd102humanUncertain significance GRCh37 chr10: 34,749,315-35,006,638 , GRCh38.p12 chr10: 34,460,387-34,717,710 ELOBP4, RPS12P16, 2 more genes
    nsv3898341copy number variation1nstd102humanUncertain significance GRCh37 chr20: 32,815,819-33,046,013 , GRCh38.p12 chr20: 34,228,013-34,458,208 ASIP, ITCH, 3 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv3912723copy number variation1nstd102humanPathogenic NCBI36 chr20: 30,288,202-45,731,170 , GRCh37.p13 chr20: 30,824,541-46,297,763 , GRCh38.p12 chr20: 32,236,738-47,669,019 ASIP, LOC107985448, 370 more genes
    nsv3913594copy number variation1nstd102humanPathogenic GRCh37 chr20: 32,020,169-35,450,284 , NCBI36 chr20: 31,483,830-34,883,698 , GRCh38 chr20: 33,432,363-36,821,881 ASIP, AHCY, 93 more genes
    nsv6311078copy number variation1nstd102humanPathogenic GRCh37 chr20: 31,189,994-34,287,210 , GRCh38.p12 chr20: 32,602,192-35,699,288 ASIP, EDEM2, 93 more genes
    nsv3906389copy number variation1nstd102humanPathogenic GRCh37 chr10: 73,232-135,524,321 , GRCh38.p12 chr10: 27,296-133,786,996 LOC100419870, LOC102724439, 2105 more genes
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