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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5979666inversion1nstd209human GRCh38 chr7: 102,358,172-102,550,712 , GRCh37.p13 chr7: 102,072,448-102,191,159 POLR2J, ALKBH4, 13 more genes
    nsv5639051insertion1nstd207human GRCh38 chr7: 102,445,084-102,445,084 , GRCh37.p13 chr7: 102,085,531-102,085,531 ORAI2
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5487004copy number variation1nstd206human GRCh38 chr7: 102,444,911-102,445,401 , GRCh37.p13 chr7: 102,085,358-102,085,848 ORAI2
    nsv5480777copy number variation1nstd206human GRCh38 chr7: 102,441,259-102,442,143 , GRCh37.p13 chr7: 102,081,706-102,082,590 ORAI2
    nsv5477798copy number variation1nstd206human GRCh38 chr7: 102,441,173-102,443,954 , GRCh37.p13 chr7: 102,081,620-102,084,401 ORAI2
    nsv5326600inversion1nstd204human GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904 , ARF5, 752 more genes
    nsv5114332mobile element insertion1nstd203human GRCh38 chr7: 102,452,954-102,452,971 , GRCh37.p13 chr7: 102,093,401-102,093,418 ORAI2
    nsv5109930mobile element insertion1nstd203human GRCh38 chr7: 102,445,677-102,445,700 , GRCh37.p13 chr7: 102,086,124-102,086,147 ORAI2
    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
    nsv4767462insertion1nstd199human GRCh37 chr7: 102,085,570-102,085,570 , GRCh38.p12 chr7: 102,445,123-102,445,123 ORAI2
    nsv4703610copy number variation1nstd195human GRCh37 chr7: 102,032,051-102,116,451 , GRCh38.p12 chr7: 102,391,604-102,476,004 POLR2J, PRKRIP1, 8 more genes
    nsv4684274copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 99,593,346-102,470,275 , GRCh38.p12 chr7: 99,995,723-102,829,828 ACHE, AP1S1, 124 more genes
    nsv4663423copy number variation1nstd186human GRCh37 chr7: 102,081,716-102,082,590 , GRCh38.p12 chr7: 102,441,269-102,442,143 ORAI2
    nsv4661707copy number variation1nstd186human GRCh37 chr7: 102,081,587-102,084,401 , GRCh38.p12 chr7: 102,441,140-102,443,954 ORAI2
    nsv4661363copy number variation1nstd186human GRCh37 chr7: 102,073,773-102,074,043 , GRCh38.p12 chr7: 102,433,326-102,433,596 ORAI2
    nsv4648626copy number variation1nstd186human GRCh37 chr7: 102,085,531-102,085,611 , GRCh38.p12 chr7: 102,445,084-102,445,164 ORAI2
    nsv4613729copy number variation1nstd183human GRCh37 chr7: 102,081,716-102,082,590 , GRCh38.p12 chr7: 102,441,269-102,442,143 ORAI2
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