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Items: 1 to 20 of 136

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4957462copy number variation1nstd200human GRCh38 chr7: 64,675,667-64,679,355 , GRCh37.p13 chr7: 64,136,045-64,139,733 ZNF107, MIR6839, 1 more genes
    nsv4957461copy number variation1nstd200human GRCh38 chr7: 64,673,881-64,817,136 , GRCh37.p13 chr7: 64,134,259-64,277,514 BNIP3P11, MIR6839, 3 more genes
    nsv4953961copy number variation1nstd200human GRCh38 chr7: 64,593,451-64,719,460 , GRCh37.p13 chr7: 64,053,829-64,179,838 BNIP3P11, LOC100128885, 3 more genes
    nsv4819323copy number variation1nstd200human GRCh37 chr7: 64,136,045-64,139,733 , GRCh38.p12 chr7: 64,675,667-64,679,355 ZNF107, MIR6839, 1 more genes
    nsv4761040inversion1nstd199human GRCh37 chr7: 55,830,732-65,288,125 , GRCh38.p12 chr7: 55,763,039-65,823,138 , CCT6A, 247 more genes
    nsv4729639copy number variation1nstd102humanUncertain significance GRCh37 chr7: 62,508,852-64,940,346 , GRCh38.p12 chr7: 63,048,474-65,475,433 VN1R39P, LOC105375324, 113 more genes
    nsv4728981copy number variation1nstd102humanUncertain significance GRCh37 chr7: 62,495,083-64,927,758 , GRCh38.p12 chr7: 63,034,705-65,462,845 LOC105375321, GUSBP6, 113 more genes
    nsv4608921copy number variation1nstd183human GRCh37 chr7: 63,448,096-64,413,552 , GRCh38.p12 chr7: 63,987,718-64,953,174 , VN1R41P, 52 more genes
    nsv4606786copy number variation1nstd183human GRCh37 chr7: 62,520,372-64,227,496 , GRCh38.p12 chr7: 63,059,994-64,767,118 , LOC105375326, 89 more genes
    nsv4606609copy number variation1nstd183human GRCh37 chr7: 64,058,602-64,162,829 , GRCh38.p12 chr7: 64,598,224-64,702,451 ZNF107, LOC100128885, 3 more genes
    nsv4525264copy number variation1nstd166human GRCh37.p13 chr7: 63,936,710-64,533,102 , GRCh38.p12 chr7: 64,476,332-65,072,724 , LOC441241, 30 more genes
    nsv4455164copy number variation1nstd102humanUncertain significance GRCh37 chr7: 63,903,253-64,426,719 , GRCh38.p12 chr7: 64,442,875-64,966,341 HNRNPCP7, EEF1DP4, 20 more genes
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 RPL23AP51, FLJ40288, 2684 more genes
    nsv4402708copy number variation1nstd174human GRCh37 chr7: 63,984,725-64,162,829 , GRCh38.p12 chr7: 64,524,347-64,702,451 LOC105375326, LOC100128885, 8 more genes
    nsv4401691copy number variation1nstd174human GRCh37 chr7: 64,133,709-64,279,274 , GRCh38.p12 chr7: 64,673,331-64,818,896 ZNF138, ZNF107, 3 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
    nsv4148569copy number variation1nstd166human GRCh37.p13 chr7: 63,973,784-64,606,144 , GRCh38.p12 chr7: 64,513,406-65,145,766 , ERV3-1-ZNF117, 30 more genes
    nsv4144178copy number variation1nstd166human GRCh37.p13 chr7: 64,109,555-64,163,556 , GRCh38.p12 chr7: 64,649,177-64,703,178 ZNF107, BNIP3P11, 1 more genes
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