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Items: 1 to 20 of 170

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5919706copy number variation1nstd209human GRCh38 chr7: 95,405,761-95,405,852 , GRCh37.p13 chr7: 95,035,073-95,035,164 PON2
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5551223insertion1nstd206human GRCh38 chr7: 95,430,330-95,430,366 , GRCh37.p13 chr7: 95,059,642-95,059,678 PON2
    nsv5486899copy number variation1nstd206human GRCh38 chr7: 95,410,006-95,419,286 , GRCh37.p13 chr7: 95,039,318-95,048,598 PON2
    nsv5478658copy number variation1nstd206human GRCh38 chr7: 95,407,922-95,409,915 , GRCh37.p13 chr7: 95,037,234-95,039,227 PON2
    nsv5381780copy number variation1nstd102humanPathogenic GRCh37 chr7: 87,477,185-100,333,327 , GRCh38.p12 chr7: 87,847,870-100,735,704 ARPC1A, LOC112267858, 265 more genes
    nsv5321926inversion1nstd204human GRCh37.p13 chr7: 93,899,155-99,360,080 , GRCh38.p13 chr7: 94,269,843-99,762,457 , CYP3A51P, 118 more genes
    nsv5116922mobile element insertion1nstd203human GRCh38 chr7: 95,430,321-95,430,330 , GRCh37.p13 chr7: 95,059,633-95,059,642 PON2
    nsv5113795mobile element insertion1nstd203human GRCh38 chr7: 95,430,320-95,430,330 , GRCh37.p13 chr7: 95,059,632-95,059,642 PON2
    nsv5109536mobile element insertion1nstd203human GRCh38 chr7: 95,430,314-95,430,330 , GRCh37.p13 chr7: 95,059,626-95,059,642 PON2
    nsv5104679mobile element insertion1nstd203human GRCh38 chr7: 95,430,315-95,430,330 , GRCh37.p13 chr7: 95,059,627-95,059,642 PON2
    nsv5102673mobile element insertion1nstd203human GRCh38 chr7: 95,430,312-95,430,330 , GRCh37.p13 chr7: 95,059,624-95,059,642 PON2
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv5029742inversion1nstd200human GRCh38 chr7: 79,688,546-147,673,588 , GRCh37.p13 chr7: 79,317,862-147,370,680 , LOC100533722, 1168 more genes
    nsv4957742copy number variation1nstd200human GRCh38 chr7: 95,430,822-95,432,077 , GRCh37.p13 chr7: 95,060,134-95,061,389 PON2
    nsv4957741copy number variation1nstd200human GRCh38 chr7: 95,425,106-95,425,172 , GRCh37.p13 chr7: 95,054,418-95,054,484 PON2
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4819624copy number variation1nstd200human GRCh37 chr7: 95,054,418-95,054,484 , GRCh38.p12 chr7: 95,425,106-95,425,172 PON2
    nsv4763531inversion1nstd199human GRCh37 chr7: 66,769,373-102,019,339 , GRCh38.p12 chr7: 67,304,386-102,378,892 , ACHE, 578 more genes
    nsv4685981copy number variation1nstd102humanPathogenic GRCh37 chr7: 93,516,132-95,668,733 , GRCh38.p12 chr7: 93,886,820-96,039,421 LOC105375404, BET1, 36 more genes
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