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Items: 1 to 20 of 159

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5890328copy number variation1nstd209human GRCh37.p13 chr3: 186,504,549-186,504,682 , GRCh38 chr3: 186,786,760-186,786,893 EIF4A2, SNORA63, 4 more genes
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv5439998copy number variation1nstd206human GRCh38 chr3: 186,786,760-186,786,895 , GRCh37.p13 chr3: 186,504,549-186,504,684 EIF4A2, SNORA63, 4 more genes
    nsv5436180copy number variation1nstd206human GRCh38 chr3: 186,783,936-186,784,012 , GRCh37.p13 chr3: 186,501,725-186,501,801 EIF4A2, SNORD2
    nsv4924973copy number variation1nstd200human GRCh38 chr3: 186,789,602-186,792,767 , GRCh37.p13 chr3: 186,507,391-186,510,556 RFC4, EIF4A2
    nsv4924972copy number variation1nstd200human GRCh38 chr3: 186,786,474-186,794,823 , GRCh37.p13 chr3: 186,504,263-186,512,612 EIF4A2, RFC4, 5 more genes
    nsv4805070copy number variation1nstd200human GRCh37 chr3: 186,507,391-186,510,556 , GRCh38.p12 chr3: 186,789,602-186,792,767 RFC4, EIF4A2
    nsv4805069copy number variation1nstd200human GRCh37 chr3: 186,504,263-186,512,612 , GRCh38.p12 chr3: 186,786,474-186,794,823 MIR1248, EIF4A2, 5 more genes
    nsv4798988copy number variation1nstd200human GRCh37 chr3: 186,506,560-186,506,884 , GRCh38.p12 chr3: 186,788,771-186,789,095 RFC4, EIF4A2
    nsv4728732copy number variation1nstd102humanLikely benign GRCh37 chr3: 186,493,742-186,668,140 , GRCh38.p12 chr3: 186,775,953-186,950,352 ADIPOQ-AS1, SNORA63, 12 more genes
    nsv4728604copy number variation1nstd102humanPathogenic GRCh37 chr3: 182,877,291-186,830,759 , GRCh38.p12 chr3: 183,159,503-187,112,971 LOC105374253, GPS2P2, 111 more genes
    nsv4683580copy number variation1nstd102humanPathogenic GRCh37 chr3: 186,256,465-187,009,440 , GRCh38.p12 chr3: 186,538,676-187,291,652 RPL39P19, FETUB, 32 more genes
    nsv4674680copy number variation1nstd102humanPathogenic GRCh37 chr3: 169,617,690-190,593,854 , GRCh38.p12 chr3: 169,899,902-190,876,065 RNU6-1120P, LOC105374262, 323 more genes
    nsv4674249copy number variation1nstd102humanPathogenic GRCh37 chr3: 185,879,162-187,446,035 , GRCh38.p12 chr3: 186,161,373-187,728,247 RTP1, RPL29P9, 43 more genes
    nsv4636423copy number variation1nstd186human GRCh37 chr3: 186,504,549-186,504,684 , GRCh38.p12 chr3: 186,786,760-186,786,895 EIF4A2, SNORA63, 4 more genes
    nsv4585440copy number variation1nstd183human GRCh37 chr3: 186,500,803-186,505,690 , GRCh38.p12 chr3: 186,783,014-186,787,901 EIF4A2, RFC4, 6 more genes
    nsv4585437copy number variation1nstd183human GRCh37 chr3: 186,394,038-186,668,229 , GRCh38.p12 chr3: 186,676,249-186,950,441 , RPS20P14, 20 more genes
    nsv4454894copy number variation1nstd102humanUncertain significance GRCh37 chr3: 186,493,742-186,672,011 , GRCh38.p12 chr3: 186,775,953-186,954,223 RPS20P14, SNORD2, 12 more genes
    nsv4453309copy number variation1nstd102humanUncertain significance GRCh37 chr3: 186,493,742-186,672,007 , GRCh38.p12 chr3: 186,775,953-186,954,219 SNORA4, RPL29P9, 12 more genes
    nsv4327395inversion1nstd166human GRCh37.p13 chr3: 126,265,569-194,265,571 , GRCh38.p12 chr3: 126,546,726-194,544,842 , ACTG1P1, 1039 more genes
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