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Items: 1 to 20 of 141

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5682059mobile element insertion1nstd211human GRCh38 chr7: 124,742,313-124,742,313 , GRCh37.p13 chr7: 124,382,367-124,382,367 GPR37
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5482214copy number variation1nstd206human GRCh38 chr7: 124,748,258-124,748,353 , GRCh37.p13 chr7: 124,388,312-124,388,407 GPR37
    nsv5400784mobile element insertion1nstd206human GRCh38 chr7: 124,742,313-124,742,364 , GRCh37.p13 chr7: 124,382,367-124,382,418 GPR37
    nsv5381759copy number variation1nstd102humanPathogenic GRCh37 chr7: 116,297,277-126,370,694 , GRCh38.p12 chr7: 116,657,223-126,730,640 TMEM229A, ST7-OT3, 110 more genes
    nsv5371148translocation1nstd200human GRCh38 chr7: 124,747,365-124,747,365 , GRCh38 chr7: 124,747,471-124,747,471 , GRCh37.p13 chr7: 124,387,419-124,387,419 , GRCh37.p13 chr7: 124,387,525-124,387,525 GPR37
    nsv5326600inversion1nstd204human GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904 , ARF5, 752 more genes
    nsv5313390copy number variation1nstd204human GRCh38.p13 chr7: 124,747,355-124,747,479 , GRCh37.p13 chr7: 124,387,409-124,387,533 GPR37
    nsv5257375copy number variation1nstd204human GRCh38.p13 chr7: 124,764,448-124,766,686 , GRCh37.p13 chr7: 124,404,502-124,406,740 GPR37
    nsv5107289mobile element insertion1nstd203human GRCh38 chr7: 124,742,297-124,742,313 , GRCh37.p13 chr7: 124,382,351-124,382,367 GPR37
    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
    nsv4968704copy number variation1nstd200human GRCh38 chr7: 124,747,012-124,889,819 , GRCh37.p13 chr7: 124,387,066-124,529,873 GPR37, LINC03043, 1 more genes
    nsv4968701copy number variation1nstd200human GRCh38 chr7: 124,661,241-124,749,652 , GRCh37.p13 chr7: 124,301,295-124,389,706 GPR37
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4675620copy number variation1nstd102humanPathogenic GRCh37 chr7: 109,251,060-159,119,707 , GRCh38.p12 chr7: 109,611,003-159,327,017 RPL26P23, ST13P17, 887 more genes
    nsv4496354mobile element insertion1nstd166human GRCh37.p13 chr7: 124,391,052-124,391,052 , GRCh38.p12 chr7: 124,750,998-124,750,998 GPR37
    nsv4487114mobile element insertion1nstd166human GRCh37.p13 chr7: 124,382,351-124,382,351 , GRCh38.p12 chr7: 124,742,297-124,742,297 GPR37
    nsv4455826copy number variation1nstd102humanPathogenic GRCh37 chr7: 121,480,906-129,389,003 , GRCh38.p12 chr7: 121,840,852-129,749,163 ASB15, PNPT1P2, 127 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
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