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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4455477copy number variation1nstd102humanPathogenic GRCh37 chr7: 80,242,420-80,303,812 , GRCh38.p12 chr7: 80,613,104-80,674,496 CD36
    nsv3920070copy number variation2nstd102humanPathogenic, Pathogenic/Likely pathogenic GRCh37 chr7: 80,256,737-80,280,613 , NCBI36 chr7: 80,094,673-80,118,549 , GRCh38 chr7: 80,627,421-80,651,297 CD36
    nsv4456269copy number variation1nstd102humanPathogenic GRCh37 chr7: 80,254,409-80,276,756 , GRCh38.p12 chr7: 80,625,093-80,647,440 CD36
    nsv4455243copy number variation1nstd102humanPathogenic GRCh37 chr7: 80,254,791-80,276,756 , GRCh38.p12 chr7: 80,625,475-80,647,440 CD36
    nsv3906813copy number variation1nstd102humanPathogenic GRCh37 chr7: 80,256,737-80,277,776 , GRCh38.p12 chr7: 80,627,421-80,648,460 CD36
    nsv4457134copy number variation1nstd102humanPathogenic GRCh37 chr7: 80,256,254-80,276,756 , GRCh38.p12 chr7: 80,626,938-80,647,440 CD36
    nsv4455112copy number variation2nstd102humanPathogenic GRCh37 chr7: 80,256,737-80,276,756 , GRCh38.p12 chr7: 80,627,421-80,647,440 CD36
    nsv4455935copy number variation1nstd102humanPathogenic GRCh37 chr7: 80,256,888-80,276,756 , GRCh38.p12 chr7: 80,627,572-80,647,440 CD36
    nsv4455151copy number variation3nstd102humanPathogenic GRCh37 chr7: 80,262,999-80,276,756 , GRCh38.p12 chr7: 80,633,683-80,647,440 CD36
    nsv6289923copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 80,279,064-80,356,762 , GRCh38.p12 chr7: 80,649,748-80,727,446 CD36
    nsv3893305copy number variation1nstd102humanLikely benign GRCh37 chr7: 80,231,693-80,299,220 , GRCh38.p12 chr7: 80,602,377-80,669,904 CD36
    nsv3902068copy number variation1nstd102humanBenign GRCh37 chr7: 80,253,911-80,279,718 , GRCh38.p12 chr7: 80,624,595-80,650,402 CD36
    nsv3891428copy number variation1nstd102humanBenign GRCh37 chr7: 80,292,426-80,307,224 , GRCh38.p12 chr7: 80,663,110-80,677,908 CD36
    nsv3893872copy number variation1nstd102humanBenign GRCh37 chr7: 80,292,448-80,307,224 , GRCh38.p12 chr7: 80,663,132-80,677,908 CD36
    nsv3890525copy number variation1nstd102humanUncertain significance GRCh37 chr7: 80,298,915-80,355,210 , GRCh38.p12 chr7: 80,669,599-80,725,894 CD36
    nsv3922939copy number variation1nstd102humanUncertain significance NCBI36 chr7: 80,079,825-80,135,626 , GRCh37.p13 chr7: 80,241,889-80,297,690 , GRCh38.p12 chr7: 80,612,573-80,668,374 CD36
    nsv4456824copy number variation2nstd102humanUncertain significance GRCh37 chr7: 80,197,285-80,276,756 , GRCh38.p12 chr7: 80,567,969-80,647,440 CD36
    nsv4675525copy number variation1nstd102humanUncertain significance GRCh37 chr7: 80,303,798-80,744,443 , GRCh38.p12 chr7: 80,674,482-81,115,127 CD36, SEMA3C
    nsv4456387copy number variation1nstd102humanUncertain significance GRCh37 chr7: 80,119,689-80,299,639 , GRCh38.p12 chr7: 80,490,373-80,670,323 CD36, GNAT3, 1 more genes
    nsv3919826copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840 CD36, RNU6-438P, 2682 more genes
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