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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112815copy number variation1nstd102humanPathogenic GRCh37 chr18: 54,285,235-77,960,815 , GRCh38.p12 chr18: 56,618,004-80,202,932 RPL31P9, TRG-TCC5-1, 271 more genes
    nsv6112802copy number variation1nstd102humanPathogenic GRCh37 chr18: 23,626,739-78,014,976 , GRCh38.p12 chr18: 26,046,775-80,257,093 RPL9P31, LINC02582, 595 more genes
    nsv5970593insertion1nstd209human GRCh38 chr18: 70,342,241-70,342,241 , GRCh37.p13 chr18: 68,009,477-68,009,477 LINC01909
    nsv5699576mobile element insertion2nstd211human GRCh38 chr18: 70,340,621-70,340,621 , GRCh37.p13 chr18: 68,007,857-68,007,857 LINC01909
    nsv5663448insertion1nstd207human GRCh38 chr18: 70,342,293-70,342,293 , GRCh37.p13 chr18: 68,009,529-68,009,529 LINC01909
    nsv5648244insertion1nstd207human GRCh38 chr18: 70,342,146-70,342,146 , GRCh37.p13 chr18: 68,009,382-68,009,382 LINC01909
    nsv5644927insertion1nstd207human GRCh38 chr18: 70,340,605-70,340,605 , GRCh37.p13 chr18: 68,007,841-68,007,841 LINC01909
    nsv5535996insertion1nstd206human GRCh38 chr18: 70,342,248-70,342,248 , GRCh37.p13 chr18: 68,009,484-68,009,484 LINC01909
    nsv5519326copy number variation1nstd206human GRCh38 chr18: 70,342,136-70,342,260 , GRCh37.p13 chr18: 68,009,372-68,009,496 LINC01909
    nsv5514135copy number variation1nstd206human GRCh38 chr18: 62,909,528-80,261,528 , GRCh37.p13 chr18: 60,576,761-78,017,154 , SMIM21, 190 more genes
    nsv5414205mobile element insertion1nstd206human GRCh38 chr18: 70,340,621-70,340,672 , GRCh37.p13 chr18: 68,007,857-68,007,908 LINC01909
    nsv5381802copy number variation1nstd102humanPathogenic GRCh37 chr18: 51,925,586-78,010,032 , GRCh38.p12 chr18: 54,399,216-80,252,149 LOC105372200, LOC105372174, 298 more genes
    nsv5165543mobile element insertion1nstd203human GRCh38 chr18: 70,340,605-70,340,621 , GRCh37.p13 chr18: 68,007,841-68,007,857 LINC01909
    nsv5018748copy number variation1nstd200human GRCh38 chr18: 70,341,114-70,347,193 , GRCh37.p13 chr18: 68,008,350-68,014,429 LINC01909
    nsv4860112copy number variation1nstd200human GRCh37 chr18: 68,015,645-68,015,986 , GRCh38.p12 chr18: 70,348,409-70,348,750 LINC01909
    nsv4758006insertion1nstd199human GRCh37 chr18: 68,009,415-68,009,415 , GRCh38.p12 chr18: 70,342,179-70,342,179 LINC01909
    nsv4729869copy number variation1nstd102humanLikely pathogenic GRCh37 chr18: 63,747,519-78,014,123 , GRCh38.p12 chr18: 66,080,283-80,256,240 CYB5A, GALR1, 147 more genes
    nsv4729838copy number variation1nstd102humanLikely pathogenic GRCh37 chr18: 65,736,299-69,297,115 , GRCh38.p12 chr18: 68,069,062-71,629,879 MTL3P, SOCS6, 31 more genes
    nsv4729787copy number variation1nstd102humanUncertain significance GRCh37 chr18: 66,697,605-69,608,331 , GRCh38.p12 chr18: 69,030,368-71,941,095 GTSCR1, LIVAR, 28 more genes
    nsv4676384copy number variation1nstd102humanPathogenic GRCh37 chr18: 63,247,046-78,014,123 , GRCh38.p12 chr18: 65,579,810-80,256,240 LINC02582, LINC01912, 149 more genes
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