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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5922766copy number variation1nstd209human GRCh38 chr7: 32,493,640-32,493,946 , GRCh37.p13 chr7: 32,533,252-32,533,558 AVL9, LSM5
    nsv5919512copy number variation1nstd209human GRCh38 chr7: 26,509,679-33,120,288 , GRCh37.p13 chr7: 26,549,298-33,159,900 , CPVL-AS1, 126 more genes
    nsv5914132copy number variation1nstd209human GRCh38 chr7: 26,936,027-36,716,695 , GRCh37.p13 chr7: 26,975,646-36,756,300 , HOXA7, 162 more genes
    nsv5635803insertion1nstd207human GRCh38 chr7: 32,495,327-32,495,327 , GRCh37.p13 chr7: 32,534,939-32,534,939 LSM5, AVL9
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5353887translocation1nstd200human GRCh38 chr11: 84,420,590-84,420,590 , GRCh38 chr7: 32,484,435-32,484,435 , GRCh37.p13 chr7: 32,524,047-32,524,047 , GRCh37.p13 chr11: 84,131,633-84,131,633 LSM5, DLG2
    nsv5040435inversion1nstd200human GRCh38 chr7: 32,354,819-33,704,107 , GRCh37.p13 chr7: 32,394,431-33,743,719 DPY19L1P1, DPY19L1P2, 20 more genes
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4882608inversion1nstd200human GRCh37 chr7: 6,326,174-37,121,976 , GRCh38.p12 chr7: 6,286,543-37,082,371 , HOXA13, 435 more genes
    nsv4674822copy number variation1nstd102humanPathogenic GRCh37 chr7: 23,877,135-33,139,446 , GRCh38.p12 chr7: 23,837,516-33,099,834 RP9P, LINC00997, 156 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
    nsv4148869copy number variation1nstd166human GRCh37.p13 chr7: 32,526,906-32,527,296 , GRCh38.p12 chr7: 32,487,294-32,487,684 LSM5
    nsv4142461copy number variation1nstd166human GRCh37.p13 chr7: 32,531,996-32,543,036 , GRCh38.p12 chr7: 32,492,384-32,503,424 AVL9, LSM5
    nsv4132473copy number variation1nstd166human GRCh37.p13 chr7: 32,528,958-32,529,931 , GRCh38.p12 chr7: 32,489,346-32,490,319 LSM5
    nsv3921383copy number variation1nstd102humanLikely pathogenic NCBI36 chr7: 30,944,510-33,407,133 , GRCh37 chr7: 30,977,985-33,440,608 , GRCh38 chr7: 30,938,370-33,400,996 ADCYAP1R1, GHRHR, 31 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
    nsv3918785copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-37,129,317 , NCBI36 chr7: 149,268-37,095,842 , GRCh38 chr7: 54,185-37,089,712 MMD2, ICA1-AS1, 554 more genes
    nsv3917886copy number variation1nstd102humanPathogenic NCBI36 chr7: 30,427,074-34,566,802 , GRCh38 chr7: 30,420,933-34,560,665 , GRCh37 chr7: 30,460,549-34,600,277 INMT, NT5C3A, 48 more genes
    nsv3915802copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-41,915,483 , GRCh38 chr7: 54,185-41,875,885 , NCBI36 chr7: 149,268-41,882,008 RPL23AP52, IQCE, 638 more genes
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