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Items: 1 to 20 of 109

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5678341mobile element insertion1nstd211human GRCh38 chr7: 44,876,005-44,876,005 , GRCh37.p13 chr7: 44,915,604-44,915,604 PURB
    nsv5636883insertion1nstd207human GRCh38 chr7: 44,883,774-44,883,774 , GRCh37.p13 chr7: 44,923,373-44,923,373 PURB
    nsv5556950sequence alteration1nstd206human GRCh38 chr7: 44,712,903-47,388,095 , GRCh37.p13 chr7: 44,752,502-47,427,692 , ADCY1, 51 more genes
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5493220copy number variation1nstd206human GRCh38 chr7: 44,883,774-44,883,827 , GRCh37.p13 chr7: 44,923,373-44,923,426 PURB
    nsv5488083copy number variation1nstd206human GRCh38 chr7: 44,885,764-44,885,818 , GRCh37.p13 chr7: 44,925,363-44,925,417 PURB
    nsv5397319mobile element insertion1nstd206human GRCh38 chr7: 44,876,005-44,876,056 , GRCh37.p13 chr7: 44,915,604-44,915,655 PURB
    nsv5381787copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,341,583-50,171,623 , GRCh38.p12 chr7: 43,301,984-50,132,027 OGDH, LOC112267918, 110 more genes
    nsv5381783copy number variation1nstd102humanPathogenic GRCh37 chr7: 41,124,364-47,945,566 , GRCh38.p12 chr7: 41,084,766-47,905,969 ELK1P1, URGCP, 121 more genes
    nsv5221233copy number variation1nstd204human GRCh38.p13 chr7: 44,597,101-45,000,100 , GRCh37.p13 chr7: 44,636,700-45,039,699 , PPIA, 14 more genes
    nsv5120028mobile element insertion1nstd203human GRCh38 chr7: 44,875,840-44,875,850 , GRCh37.p13 chr7: 44,915,439-44,915,449 PURB
    nsv5112231mobile element insertion1nstd203human GRCh38 chr7: 44,876,005-44,876,005 , GRCh37.p13 chr7: 44,915,604-44,915,604 PURB
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4617818copy number variation1nstd183human GRCh37 chr7: 44,915,907-44,918,039 , GRCh38.p12 chr7: 44,876,308-44,878,440 PURB
    nsv4605055copy number variation1nstd183human GRCh37 chr7: 44,916,114-44,923,159 , GRCh38.p12 chr7: 44,876,515-44,883,560 MIR4657, PURB
    nsv4490238mobile element insertion1nstd166human GRCh37.p13 chr7: 44,915,439-44,915,439 , GRCh38.p12 chr7: 44,875,840-44,875,840 PURB
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 RPL23AP51, FLJ40288, 2684 more genes
    nsv4352523inversion1nstd102humanPathogenic GRCh37 chr7: 20,954,043-114,556,605 , GRCh38.p12 chr7: 20,914,424-114,916,550 ACHE, ADCY1, 1532 more genes
    nsv4133210copy number variation1nstd166human GRCh37.p13 chr7: 44,922,500-44,927,500 , GRCh38.p12 chr7: 44,882,901-44,887,901 PURB
    nsv3924742copy number variation1nstd102humanPathogenic GRCh37 chr7: 38,217,601-45,343,699 , GRCh38 chr7: 38,177,999-45,304,100 , NCBI36 chr7: 38,184,126-45,310,224 NUDCD3, KRT8P20, 152 more genes
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