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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5558142mobile element insertion1nstd206human GRCh38 chr2: 102,295,972-141,288,199 , GRCh37.p13 chr2: 102,912,432-142,045,768 , LOC105373587, 623 more genes
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5361068translocation1nstd200human GRCh38 chr2: 119,370,185-119,370,185 , GRCh38 chr2: 119,371,043-119,371,043 , GRCh37.p13 chr2: 120,128,619-120,128,619 , GRCh37.p13 chr2: 120,127,761-120,127,761 DBI
    nsv5338167translocation1nstd200human GRCh37 chr2: 120,128,619-120,128,619 , GRCh37 chr2: 120,127,761-120,127,761 , GRCh38.p12 chr2: 119,370,185-119,370,185 , GRCh38.p12 chr2: 119,371,043-119,371,043 DBI
    nsv5292777copy number variation1nstd204human GRCh37.p13 chr2: 120,101,316-120,449,316 , GRCh38.p13 chr2: 119,343,740-119,691,740 DBI, SCTR, 5 more genes
    nsv5201752copy number variation1nstd204human GRCh38.p13 chr2: 119,340,935-119,370,510 , GRCh37.p13 chr2: 120,098,511-120,128,086 C2orf76, DBI
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv5033955inversion1nstd200human GRCh38 chr2: 103,800,446-187,202,765 , GRCh37.p13 chr2: 104,416,904-188,067,492 , EDDM3CP, 1184 more genes
    nsv4923889copy number variation1nstd200human GRCh38 chr2: 119,343,749-119,691,732 , GRCh37.p13 chr2: 120,101,325-120,449,308 SCTR, DBI, 5 more genes
    nsv4915230copy number variation1nstd200human GRCh38 chr2: 118,753,385-119,992,729 , GRCh37.p13 chr2: 119,510,961-120,750,305 TMEM177, TMEM37, 17 more genes
    nsv4879764inversion1nstd200human GRCh37 chr2: 104,416,904-188,067,492 , GRCh38.p12 chr2: 103,800,446-187,202,765 , ACMSD, 1184 more genes
    nsv4781743copy number variation1nstd200human GRCh37 chr2: 120,101,325-120,449,308 , GRCh38.p12 chr2: 119,343,749-119,691,732 DBI, C2orf76, 5 more genes
    nsv4743379copy number variation1nstd199human GRCh37 chr2: 88,481,090-124,440,189 , GRCh38.p12 chr9: 40,649,751-63,450,622 , GRCh38.p12 chr9: 40,649,907-63,450,751 , GRCh38.p12 chr1: 125,085,511-144,884,066 , GRCh38.p12 chr2: 88,181,571-123,682,613 , EIF2AK3, 861 more genes
    nsv4674739copy number variation1nstd102humanPathogenic GRCh37 chr2: 118,903,294-123,099,547 , GRCh38.p12 chr2: 118,145,718-122,341,971 LOC101927709, NIFK-AS1, 55 more genes
    nsv4674710copy number variation1nstd102humanPathogenic GRCh37 chr2: 118,872,395-128,069,813 , GRCh38.p12 chr2: 118,114,819-127,312,237 C2orf76, LOC107985817, 89 more genes
    nsv4674248copy number variation1nstd102humanLikely benign GRCh37 chr2: 119,859,810-120,157,980 , GRCh38.p12 chr2: 119,102,234-119,400,404 DBI, STEAP3, 6 more genes
    nsv4674062copy number variation1nstd102humanPathogenic GRCh37 chr2: 115,416,190-122,399,064 , GRCh38.p12 chr2: 114,658,613-121,641,488 DPP10-AS3, HTR5BP, 71 more genes
    nsv4519384copy number variation1nstd166human GRCh37.p13 chr2: 119,819,998-124,091,000 , GRCh38.p12 chr2: 119,062,422-123,333,424 LOC105373593, LOC105373596, 54 more genes
    nsv4374974copy number variation1nstd173human GRCh37 chr2: 119,695,253-120,289,518 , GRCh38.p12 chr2: 118,937,677-119,531,942 C2orf76, C1QL2, 10 more genes
    nsv4075407copy number variation1nstd166human GRCh37.p13 chr2: 120,125,184-120,125,374 , GRCh38.p12 chr2: 119,367,608-119,367,798 DBI
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