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Items: 1 to 20 of 148

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7050777inversion1nstd229human GRCh38 chr2: 117,420,323-122,585,255 , GRCh37.p13 chr2: 118,177,899-123,342,831 LOC105373578, RPL17P15, 65 more genes
    nsv7044064inversion1nstd229human GRCh38 chr2: 112,019,946-120,004,832 , GRCh37.p13 chr2: 112,777,523-120,762,408 LOC105373563, IL1A, 112 more genes
    nsv6685761copy number variation1nstd229human GRCh38 chr2: 119,391,683-119,531,219 , GRCh37.p13 chr2: 120,149,259-120,288,795 SCTR, SCTR-AS1, 1 more genes
    nsv6679459copy number variation1nstd229human GRCh38 chr2: 119,311,516-119,861,317 , GRCh37.p13 chr2: 120,069,092-120,618,893 RPL17P15, TMEM177, 8 more genes
    nsv6636976copy number variation1nstd102humanUncertain significance GRCh37 chr2: 120,079,538-120,626,557 , GRCh38.p12 chr2: 119,321,962-119,868,981 TMEM177, RPL17P15, 8 more genes
    nsv6636871copy number variation1nstd102humanPathogenic GRCh37 chr2: 116,761,476-123,897,262 , GRCh38.p12 chr2: 116,003,900-123,139,686 LOC105373578, RPL17P15, 78 more genes
    nsv6553311inversion1nstd223human GRCh38 chr2: 113,382,126-121,687,299 , GRCh37.p13 chr2: 114,139,703-122,444,875 RPSAP23, CCDC93, 98 more genes
    nsv6349537copy number variation1nstd223human GRCh38 chr2: 119,247,614-119,525,129 , GRCh37.p13 chr2: 120,005,190-120,282,705 SCTR, C2orf76, 6 more genes
    nsv6342612copy number variation1nstd223human GRCh38 chr2: 119,319,204-119,873,037 , GRCh37.p13 chr2: 120,076,780-120,630,613 PTPN4, CFAP221, 8 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6314748copy number variation1nstd102humanPathogenic GRCh37 chr2: 112,475,655-145,691,999 , GRCh38.p12 chr2: 111,718,078-144,934,432 MED15P9, TMEM37, 474 more genes
    nsv6314726copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196 ACTG2, ACYP2, 1713 more genes
    nsv6313770copy number variation1nstd102humanPathogenic GRCh37 chr2: 113,188,197-128,144,700 , GRCh38.p12 chr2: 112,430,620-127,387,124 LOC105373575, RPS20P11, 174 more genes
    nsv6291353copy number variation1nstd102humanPathogenic GRCh37 chr2: 111,484,468-146,333,604 , GRCh38.p12 chr2: 110,726,891-145,576,036 LINC01120, LOC105373585, 490 more genes
    nsv6290805copy number variation1nstd102humanUncertain significance GRCh37 chr2: 119,967,365-121,555,029 , GRCh38.p12 chr2: 119,209,789-120,797,453 LOC101927764, MTND5P28, 29 more genes
    nsv6134420copy number variation1nstd213human GRCh37 chr2: 117,140,000-144,230,001 , GRCh38.p12 chr2: 116,382,424-143,472,432 BIN1, CCNT2, 382 more genes
    nsv6134238copy number variation1nstd213human GRCh37 chr2: 119,730,000-120,490,001 , GRCh38.p12 chr2: 118,972,424-119,732,425 DBI, SCTR, 14 more genes
    nsv5831121copy number variation1nstd209human GRCh38 chr2: 119,407,244-119,444,066 , GRCh37.p13 chr2: 120,164,820-120,201,642 TMEM37, SCTR
    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
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