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Items: 1 to 20 of 217

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5564425copy number variation1nstd102humanUncertain significance GRCh37 chr2: 108,604,612-109,336,154 , GRCh38.p12 chr2: 107,988,156-108,719,698 LIMS1-AS1, SETD6P1, 18 more genes
    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
    nsv5446121copy number variation1nstd206human GRCh38 chr2: 107,891,618-108,660,859 , GRCh37.p13 chr2: 108,508,074-109,277,315 RPL22P8, ACTP1, 17 more genes
    nsv5361005translocation1nstd200human GRCh38 chr2: 108,286,211-108,286,211 , GRCh38 chr2: 108,291,401-108,291,401 , GRCh37.p13 chr2: 108,902,667-108,902,667 , GRCh37.p13 chr2: 108,907,857-108,907,857 SULT1C2
    nsv5333993translocation1nstd200human GRCh37 chr2: 108,902,678-108,902,678 , GRCh37 chr2: 108,908,050-108,908,050 , GRCh38.p12 chr2: 108,286,222-108,286,222 , GRCh38.p12 chr2: 108,291,594-108,291,594 SULT1C2
    nsv5332414translocation1nstd200human GRCh37 chr2: 108,902,667-108,902,667 , GRCh37 chr2: 108,907,857-108,907,857 , GRCh38.p12 chr2: 108,286,211-108,286,211 , GRCh38.p12 chr2: 108,291,401-108,291,401 SULT1C2
    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
    nsv4914949copy number variation1nstd200human GRCh38 chr2: 108,293,403-108,295,004 , GRCh37.p13 chr2: 108,909,859-108,911,460 SULT1C2
    nsv4914948copy number variation1nstd200human GRCh38 chr2: 108,293,046-108,294,399 , GRCh37.p13 chr2: 108,909,502-108,910,855 SULT1C2
    nsv4884636inversion1nstd200human GRCh37 chr2: 106,977,042-109,816,306 , GRCh38.p12 chr2: 106,360,586-109,199,850 , SULT1C3, 44 more genes
    nsv4879764inversion1nstd200human GRCh37 chr2: 104,416,904-188,067,492 , GRCh38.p12 chr2: 103,800,446-187,202,765 , ACMSD, 1184 more genes
    nsv4786813copy number variation1nstd200human GRCh37 chr2: 108,909,502-108,910,855 , GRCh38.p12 chr2: 108,293,046-108,294,399 SULT1C2
    nsv4766632inversion1nstd199human GRCh37 chr2: 87,997,505-112,010,501 , GRCh38.p12 chr1: 125,085,511-144,884,066 , GRCh38.p12 chr2: 87,697,986-111,252,924 , GRCh38.p12 chr9: 40,649,907-63,450,751 , GRCh38.p12 chr9: 40,649,751-63,450,622 , ADRA2B, 706 more genes
    nsv4752571inversion1nstd199human GRCh37 chr2: 87,550,795-112,295,517 , GRCh38.p12 chr1: 125,085,511-144,884,066 , GRCh38.p12 chr2: 87,323,672-111,537,940 , GRCh38.p12 chr9: 40,649,907-63,450,751 , GRCh38.p12 chr9: 40,649,751-63,450,622 , ADRA2B, 723 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
    nsv4728410copy number variation1nstd102humanPathogenic GRCh37 chr2: 107,029,680-113,187,742 , GRCh38.p12 chr2: 106,413,224-112,430,165 RPL10P5, BUB1, 121 more genes
    nsv4683958copy number variation2nstd102humanUncertain significance GRCh37 chr2: 108,604,602-109,579,739 , GRCh38.p12 chr2: 107,988,146-108,963,283 RANBP2, LIMS1-AS1, 21 more genes
    nsv4674320copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 108,499,809-110,504,318 , GRCh38.p12 chr2: 107,883,353-109,746,741 LIMS1, RANBP2, 37 more genes
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