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Items: 1 to 20 of 218

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5672896copy number variation1nstd102humanPathogenic GRCh37 chr18: 2,656,075-13,885,536 , GRCh38.p12 chr18: 2,656,076-13,885,537 RN7SL862P, LOC105371972, 181 more genes
    nsv5520806copy number variation1nstd206human GRCh38 chr18: 9,332,000-10,232,000 , GRCh37.p13 chr18: 9,331,998-10,231,997 RALBP1, RAB31, 21 more genes
    nsv5148234mobile element insertion1nstd203human GRCh38 chr18: 9,884,635-9,884,660 , GRCh37.p13 chr18: 9,884,632-9,884,657 TXNDC2
    nsv5014271copy number variation1nstd200human GRCh38 chr18: 9,881,274-9,894,244 , GRCh37.p13 chr18: 9,881,271-9,894,241 PIGPP4, LOC105371982, 1 more genes
    nsv5014269copy number variation1nstd200human GRCh38 chr18: 9,868,079-9,893,207 , GRCh37.p13 chr18: 9,868,076-9,893,204 PIGPP4, TXNDC2
    nsv4854532copy number variation1nstd200human GRCh37 chr18: 9,868,076-9,893,204 , GRCh38.p12 chr18: 9,868,079-9,893,207 PIGPP4, TXNDC2
    nsv4729915copy number variation1nstd102humanPathogenic GRCh37 chr18: 7,598,173-15,422,644 , GRCh38.p12 chr18: 7,598,175-15,410,899 CEP192, RNU2-27P, 155 more genes
    nsv4676396copy number variation1nstd102humanPathogenic GRCh37 chr18: 971,295-11,250,447 , GRCh38.p12 chr18: 971,294-11,250,448 LOC100129774, LOC100419892, 146 more genes
    nsv4676393copy number variation1nstd102humanPathogenic GRCh37 chr18: 13,034-15,330,525 , GRCh38.p12 chr18: 13,034-15,330,526 PRELID3A, ANKRD30B, 275 more genes
    nsv4676314copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,304-15,143,714 , GRCh38.p12 chr18: 136,304-15,143,715 EIF4A2P1, PMM2P2, 263 more genes
    nsv4676159copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,226-13,894,429 , GRCh38.p12 chr18: 136,226-13,894,430 SLC25A51P2, BOLA2P1, 221 more genes
    nsv4676141copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,226-18,529,578 , GRCh38.p12 chr18: 136,226-20,949,617 ANKRD12, DLGAP1-AS1, 270 more genes
    nsv4385858copy number variation1nstd173human GRCh37 chr18: 136,227-18,529,578 , GRCh38.p12 chr18: 136,227-20,949,617 , LOC105371995, 276 more genes
    nsv4348774copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,226-15,175,005 , GRCh38.p12 chr18: 136,226-15,175,006 ANKRD62, LOC100419892, 263 more genes
    nsv4269906copy number variation1nstd166human GRCh37.p13 chr18: 9,880,000-9,902,000 , GRCh38.p12 chr18: 9,880,003-9,902,003 PIGPP4, LOC105371982, 1 more genes
    nsv3967587copy number variation1nstd168human GRCh38 chr18: 9,885,536-9,927,494 , GRCh37.p13 chr18: 9,885,533-9,927,491 VAPA, RNA5SP450, 2 more genes
    nsv3956183insertion1nstd168human GRCh38 chr18: 9,884,444-9,885,536 , GRCh37.p13 chr18: 9,884,441-9,885,533 TXNDC2
    nsv3934806copy number variation1nstd167human GRCh37 chr18: 9,887,388-9,887,433 , GRCh38.p12 chr18: 9,887,391-9,887,436 TXNDC2
    nsv3924832copy number variation1nstd102humanPathogenic NCBI36 chr18: 4,275-12,801,387 , GRCh37.p13 chr18: 14,275-12,811,387 , GRCh38.p12 chr18: 14,275-12,811,388 PIEZO2, LINC01882, 211 more genes
    nsv3924706copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,227-78,014,123 , GRCh38 chr18: 136,227-80,256,240 , NCBI36 chr18: 126,227-76,115,097 LOC100420948, NPM1P2, 941 more genes
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