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Items: 1 to 20 of 114

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5677194mobile element insertion1nstd211human GRCh38 chr5: 163,448,274-163,448,274 , GRCh37.p13 chr5: 162,875,280-162,875,280 CCNG1, NUDCD2
    nsv5675980mobile element insertion2nstd211human GRCh38 chr5: 163,446,471-163,446,471 , GRCh37.p13 chr5: 162,873,477-162,873,477 NUDCD2, CCNG1
    nsv5640507insertion1nstd207human GRCh38 chr5: 163,446,457-163,446,457 , GRCh37.p13 chr5: 162,873,463-162,873,463 CCNG1, NUDCD2
    nsv5403695mobile element insertion1nstd206human GRCh38 chr5: 163,446,471-163,446,522 , GRCh37.p13 chr5: 162,873,477-162,873,528 CCNG1, NUDCD2
    nsv5400732mobile element insertion1nstd206human GRCh38 chr5: 163,448,274-163,448,325 , GRCh37.p13 chr5: 162,875,280-162,875,331 CCNG1, NUDCD2
    nsv5301541copy number variation1nstd204human GRCh38.p13 chr5: 163,429,687-163,899,395 , GRCh37.p13 chr5: 162,856,693-163,326,401 CCNG1, HMMR-AS1, 8 more genes
    nsv5238056copy number variation1nstd204human GRCh38.p13 chr5: 163,435,672-163,459,185 , GRCh37.p13 chr5: 162,862,678-162,886,191 LOC105377700, NUDCD2, 2 more genes
    nsv5220639copy number variation1nstd204human GRCh38.p13 chr5: 163,430,401-163,899,400 , GRCh37.p13 chr5: 162,857,407-163,326,406 HMMR, CCNG1, 8 more genes
    nsv4939642copy number variation1nstd200human GRCh38 chr5: 163,459,076-163,459,175 , GRCh37.p13 chr5: 162,886,082-162,886,181 HMMR, NUDCD2
    nsv4684271copy number variation1nstd102humanUncertain significance GRCh37 chr5: 161,880,996-162,958,461 , GRCh38.p12 chr5: 162,453,990-163,531,455 MRPL57P6, ARL2BPP5, 10 more genes
    nsv4674945copy number variation1nstd102humanPathogenic GRCh37 chr5: 156,347,980-169,959,880 , GRCh38.p12 chr5: 156,920,969-170,532,876 LINC02227, LINC01932, 146 more genes
    nsv4597863copy number variation1nstd183human GRCh37 chr5: 162,537,788-163,536,134 , GRCh38.p12 chr5: 163,110,782-164,109,128 LOC102724458, NUDCD2, 8 more genes
    nsv4493594mobile element insertion1nstd166human GRCh37.p13 chr5: 162,873,463-162,873,463 , GRCh38.p12 chr5: 163,446,457-163,446,457 CCNG1, NUDCD2
    nsv4493372mobile element insertion1nstd166human GRCh37.p13 chr5: 162,875,264-162,875,264 , GRCh38.p12 chr5: 163,448,258-163,448,258 NUDCD2, CCNG1
    nsv4456207copy number variation1nstd102humanUncertain significance GRCh37 chr5: 162,636,748-163,072,415 , GRCh38.p12 chr5: 163,209,742-163,645,409 NUDCD2, HMMR-AS1, 4 more genes
    nsv4455586copy number variation1nstd102humanPathogenic GRCh37 chr5: 156,597,181-171,166,353 , GRCh38.p12 chr5: 157,170,170-171,739,349 LOC105377677, GABRA6, 164 more genes
    nsv4132129copy number variation1nstd166human GRCh37.p13 chr5: 162,885,010-162,885,607 , GRCh38.p12 chr5: 163,458,004-163,458,601 NUDCD2
    nsv4126739copy number variation1nstd166human GRCh37.p13 chr5: 162,830,343-162,904,671 , GRCh38.p12 chr5: 163,403,337-163,477,665 NUDCD2, LOC105377700, 2 more genes
    nsv4126056copy number variation1nstd166human GRCh37.p13 chr5: 159,698,170-166,152,496 , GRCh38.p12 chr5: 160,271,163-166,725,491 , MIR3142, 49 more genes
    nsv3965580copy number variation1nstd168human GRCh38 chr5: 163,426,474-163,462,928 , GRCh37.p13 chr5: 162,853,480-162,889,934 NUDCD2, HMMR, 2 more genes
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