U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 128

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5902546copy number variation1nstd209human GRCh38 chr2: 114,736,183-114,845,103 , GRCh37.p13 chr2: 115,493,760-115,602,680 DPP10-AS3, DPP10
    nsv5887713copy number variation1nstd209human GRCh38 chr2: 114,826,049-114,835,462 , GRCh37.p13 chr2: 115,583,626-115,593,039 DPP10, DPP10-AS3
    nsv5831180copy number variation1nstd209human GRCh38 chr2: 114,825,874-114,831,487 , GRCh37.p13 chr2: 115,583,451-115,589,064 DPP10-AS3, DPP10
    nsv5676055mobile element insertion1nstd211human GRCh38 chr2: 114,833,099-114,833,099 , GRCh37.p13 chr2: 115,590,676-115,590,676 DPP10-AS3, DPP10
    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
    nsv5446134copy number variation1nstd206human GRCh38 chr2: 114,366,072-114,835,483 , GRCh37.p13 chr2: 115,123,649-115,593,060 DPP10-AS3, RNU2-41P, 1 more genes
    nsv5398710mobile element insertion1nstd206human GRCh38 chr2: 114,833,099-114,833,103 , GRCh37.p13 chr2: 115,590,676-115,590,680 DPP10-AS3, DPP10
    nsv5063929mobile element insertion1nstd203human GRCh38 chr2: 114,829,856-114,829,868 , GRCh37.p13 chr2: 115,587,433-115,587,445 DPP10, DPP10-AS3
    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
    nsv4879764inversion1nstd200human GRCh37 chr2: 104,416,904-188,067,492 , GRCh38.p12 chr2: 103,800,446-187,202,765 , ACMSD, 1184 more genes
    nsv4786920copy number variation1nstd200human GRCh37 chr2: 115,583,629-115,593,040 , GRCh38.p12 chr2: 114,826,052-114,835,463 DPP10, DPP10-AS3
    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
    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
    nsv4462646mobile element insertion1nstd166human GRCh37.p13 chr2: 115,590,661-115,590,661 , GRCh38.p12 chr2: 114,833,084-114,833,084 DPP10-AS3, DPP10
    nsv4378736copy number variation1nstd173human GRCh37 chr2: 115,121,259-115,593,610 , GRCh38.p12 chr2: 114,363,682-114,836,033 DPP10, RNU2-41P, 1 more genes
    nsv3923963copy number variation1nstd102humanUncertain significance NCBI36 chr2: 110,190,938-242,751,149 , GRCh37.p13 chr2: 110,833,649-243,102,476 , GRCh38.p12 chr2: 110,076,072-242,160,331 NMTRQ-TTG9-1, MIR6810, 1944 more genes
    nsv3921207copy number variation1nstd102humanPathogenic NCBI36 chr2: 110,857,227-116,449,787 , GRCh37.p13 chr2: 111,334,455-116,733,317 , GRCh38.p12 chr2: 110,576,878-115,975,741 RABL2A, RPL34P8, 98 more genes
    nsv3910630copy number variation1nstd102humanPathogenic NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331 DAZAP2P1, RPL36AP16, 2991 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center