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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5977915inversion1nstd209human GRCh38 chr7: 86,525,777-88,855,329 , GRCh37.p13 chr7: 86,155,093-88,484,643 , GRM3, 31 more genes
    nsv5973961inversion1nstd209human GRCh37.p13 chr7: 87,707,926-88,185,252 , GRCh38 chr7: 88,078,611-88,555,937 SRI, ADAM22, 7 more genes
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    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
    nsv4763531inversion1nstd199human GRCh37 chr7: 66,769,373-102,019,339 , GRCh38.p12 chr7: 67,304,386-102,378,892 , ACHE, 578 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
    nsv4352523inversion1nstd102humanPathogenic GRCh37 chr7: 20,954,043-114,556,605 , GRCh38.p12 chr7: 20,914,424-114,916,550 ACHE, ADCY1, 1532 more genes
    nsv4138857copy number variation1nstd166human GRCh37.p13 chr7: 88,037,049-88,212,629 , GRCh38.p12 chr7: 88,407,734-88,583,314 PET117P1, EIF4A1P13, 2 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
    nsv3919481copy number variation1nstd102humanUncertain significance NCBI36 chr7: 87,598,611-87,987,353 , GRCh37 chr7: 87,760,675-88,149,417 , GRCh38 chr7: 88,131,360-88,520,102 PET117P1, LOC100419447, 7 more genes
    nsv3917092copy number variation1nstd102humanLikely pathogenic NCBI36 chr7: 86,846,728-91,199,124 , GRCh37 chr7: 87,008,792-91,361,188 , GRCh38 chr7: 87,379,476-91,731,873 CDK14, ABCB1, 44 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
    nsv3909111copy number variation1nstd102humanUncertain significance GRCh37 chr7: 87,482,666-89,449,405 , GRCh38.p12 chr7: 87,853,351-89,820,091 DBF4, EIF4A1P13, 18 more genes
    nsv3909087copy number variation1nstd102humanPathogenic GRCh37 chr7: 44,935-159,126,310 , GRCh38.p12 chr7: 44,935-159,333,620 MNX1-AS2, VN1R31P, 2682 more genes
    nsv3908592copy number variation2nstd102humanPathogenic GRCh37 chr7: 43,361-159,119,707 , GRCh38.p12 chr7: 43,361-159,327,017 TRGV3, SNX10-AS1, 2682 more genes
    nsv3894780copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,704-159,122,532 , GRCh38.p12 chr7: 10,704-159,329,842 RNU6-565P, LAMB1, 2684 more genes
    nsv3888815copy number variation1nstd102humanPathogenic GRCh37 chr7: 12,258,147-140,494,267 , GRCh38.p12 chr7: 12,218,521-140,794,467 LOC107986817, DNAJB9, 2014 more genes
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