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Items: 1 to 20 of 173

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5663516insertion1nstd207human GRCh38 chr12: 8,062,958-8,062,958 , GRCh37.p13 chr12: 8,215,554-8,215,554 C3AR1
    nsv5650668insertion1nstd207human GRCh38 chr12: 8,060,991-8,060,991 , GRCh37.p13 chr12: 8,213,587-8,213,587 C3AR1
    nsv5499035copy number variation1nstd206human GRCh38 chr12: 7,853,043-8,060,132 , GRCh37.p13 chr12: 8,005,639-8,212,728 SLC2A14, NANOGP1, 8 more genes
    nsv5323122inversion1nstd204human GRCh37.p13 chr12: 6,338,815-22,046,498 , GRCh38.p13 chr12: 6,229,649-21,893,564 , A2M, 414 more genes
    nsv5264993copy number variation1nstd204human GRCh38.p13 chr12: 8,042,101-8,085,800 , GRCh37.p13 chr12: 8,194,697-8,238,396 NECAP1, C3AR1, 1 more genes
    nsv5029743inversion1nstd200human GRCh38 chr12: 7,297,013-15,308,349 , GRCh37.p13 chr12: 7,449,609-15,461,283 , MIR1244-4, 259 more genes
    nsv4972101copy number variation1nstd200human GRCh38 chr12: 8,053,436-8,058,383 , GRCh37.p13 chr12: 8,206,032-8,210,979 FOXJ2, C3AR1
    nsv4882300inversion1nstd200human GRCh37 chr12: 6,338,820-22,046,498 , GRCh38.p12 chr12: 6,229,654-21,893,564 , LOC105369686, 414 more genes
    nsv4833816copy number variation1nstd200human GRCh37 chr12: 8,206,032-8,210,979 , GRCh38.p12 chr12: 8,053,436-8,058,383 C3AR1, FOXJ2
    nsv4729082copy number variation1nstd102humanLikely benign GRCh37 chr12: 7,755,907-8,436,318 , GRCh38.p12 chr12: 7,603,311-8,283,722 NANOGP1, RPS20P29, 29 more genes
    nsv4682301copy number variation1nstd102humanUncertain significance GRCh37 chr12: 6,945,914-8,248,706 , GRCh38.p12 chr12: 6,836,750-8,096,110 SPSB2, LOC100131676, 57 more genes
    nsv4681373copy number variation1nstd102humanUncertain significance GRCh37 chr12: 7,842,454-8,248,706 , GRCh38.p12 chr12: 7,689,858-8,096,110 NANOGP1, LOC100462988, 14 more genes
    nsv4674941copy number variation1nstd102humanPathogenic GRCh37 chr12: 274,676-37,869,301 , GRCh38.p12 chr12: 165,510-37,475,499 LOC105376675, ATF7IP, 682 more genes
    nsv4669006copy number variation1nstd186human GRCh37 chr12: 8,000,122-8,216,726 , GRCh38.p12 chr12: 7,847,526-8,064,130 LOC100130582, C3AR1, 8 more genes
    nsv4658022copy number variation1nstd186human GRCh37 chr12: 8,000,122-8,216,726 , GRCh38.p12 chr12: 7,847,526-8,064,130 NANOGP1, LOC100462988, 8 more genes
    nsv4607420copy number variation1nstd183human GRCh37 chr12: 7,770,684-8,556,693 , GRCh38.p12 chr12: 7,618,088-8,404,097 DEFB109F, FAM66C, 32 more genes
    nsv4601445copy number variation1nstd183human GRCh37 chr12: 8,115,941-8,245,645 , GRCh38.p12 chr12: 7,963,345-8,093,049 C3AR1, NECAP1, 4 more genes
    nsv4455658copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,786-8,393,815 , GRCh38.p12 chr12: 64,620-8,241,219 PLEKHG6, MIR141, 226 more genes
    nsv4455458copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,786-34,496,628 , GRCh38.p12 chr12: 64,620-34,343,693 EMP1, PLBD1-AS1, 684 more genes
    nsv4455042copy number variation4nstd102humanUncertain significance GRCh37 chr12: 6,945,914-9,027,627 , GRCh38.p12 chr12: 6,836,750-8,875,031 HADHAP2, CLEC6A, 91 more genes
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