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Items: 1 to 20 of 105

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5718822mobile element insertion1nstd211human GRCh38 chr7: 91,872,766-91,872,766 , GRCh37.p13 chr7: 91,502,080-91,502,080 MTERF1
    nsv5563019sequence alteration1nstd206human GRCh38 chr7: 91,857,662-91,893,869 , GRCh37.p13 chr7: 91,486,976-91,523,183 MTERF1, LOC112267986
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5555297mobile element insertion1nstd206human GRCh38 chr7: 91,872,766-91,872,769 , GRCh37.p13 chr7: 91,502,080-91,502,083 MTERF1
    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
    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
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4825160copy number variation1nstd200human GRCh37 chr7: 91,499,562-91,500,201 , GRCh38.p12 chr7: 91,870,248-91,870,887 MTERF1
    nsv4763531inversion1nstd199human GRCh37 chr7: 66,769,373-102,019,339 , GRCh38.p12 chr7: 67,304,386-102,378,892 , ACHE, 578 more genes
    nsv4616941copy number variation1nstd183human GRCh37 chr7: 91,170,449-91,743,150 , GRCh38.p12 chr7: 91,541,134-92,113,836 MTERF1, CYP51A1, 2 more genes
    nsv4523924copy number variation1nstd166human GRCh37.p13 chr7: 90,941,478-91,732,937 , GRCh38.p12 chr7: 91,312,163-92,103,623 MTERF1, AKAP9, 5 more genes
    nsv4485355mobile element insertion1nstd166human GRCh37.p13 chr7: 91,509,256-91,509,256 , GRCh38.p12 chr7: 91,879,942-91,879,942 LOC112267986, MTERF1
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 RPL23AP51, FLJ40288, 2684 more genes
    nsv4376491copy number variation1nstd173human GRCh37 chr7: 91,510,317-91,532,715 , GRCh38.p12 chr7: 91,881,003-91,903,401 LOC112267986, MTERF1
    nsv4352523inversion1nstd102humanPathogenic GRCh37 chr7: 20,954,043-114,556,605 , GRCh38.p12 chr7: 20,914,424-114,916,550 ACHE, ADCY1, 1532 more genes
    nsv4339493sequence alteration1nstd166human GRCh37.p13 chr7: 90,941,478-91,733,634 , GRCh38.p12 chr7: 91,312,163-92,104,320 MTERF1, AKAP9, 5 more genes
    nsv3922072copy number variation1nstd102humanUncertain significance NCBI36 chr7: 91,344,065-91,518,192 , GRCh37.p13 chr7: 91,506,129-91,680,256 , GRCh38.p12 chr7: 91,876,815-92,050,942 LOC112267986, AKAP9, 1 more genes
    nsv3919826copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840 RNU6-438P, LOC105375300, 2682 more genes
    nsv3914094copy number variation1nstd102humanPathogenic GRCh38 chr7: 84,002,634-95,228,883 , GRCh37 chr7: 83,631,950-94,858,195 , NCBI36 chr7: 83,469,886-94,696,131 LINC03017, MIR1285-1, 121 more genes
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