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Items: 1 to 20 of 198

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5607840insertion1nstd207human GRCh38 chr2: 119,254,050-119,254,050 , GRCh37.p13 chr2: 120,011,626-120,011,626 STEAP3
    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
    nsv5450963copy number variation1nstd206human GRCh38 chr2: 119,259,683-119,259,792 , GRCh37.p13 chr2: 120,017,259-120,017,368 STEAP3
    nsv5380604translocation1nstd200human GRCh38 chr22: 23,853,610-23,853,610 , GRCh38 chr2: 119,243,698-119,243,698 , GRCh37.p13 chr2: 120,001,274-120,001,274 , GRCh37.p13 chr22: 24,195,797-24,195,797 STEAP3, STEAP3-AS1
    nsv5295952copy number variation1nstd204human GRCh38.p13 chr2: 119,256,753-119,260,540 , GRCh37.p13 chr2: 120,014,329-120,018,116 STEAP3
    nsv5213956copy number variation1nstd204human GRCh38.p13 chr2: 119,256,769-119,260,584 , GRCh37.p13 chr2: 120,014,345-120,018,160 STEAP3
    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
    nsv4915243copy number variation1nstd200human GRCh38 chr2: 119,233,506-119,233,631 , GRCh37.p13 chr2: 119,991,082-119,991,207 STEAP3
    nsv4915242copy number variation1nstd200human GRCh38 chr2: 119,227,995-119,229,263 , GRCh37.p13 chr2: 119,985,571-119,986,839 STEAP3
    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
    nsv4787033copy number variation1nstd200human GRCh37 chr2: 119,991,082-119,991,207 , GRCh38.p12 chr2: 119,233,506-119,233,631 STEAP3
    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
    nsv4674201copy number variation1nstd102humanUncertain significance GRCh37 chr2: 119,905,466-120,016,024 , GRCh38.p12 chr2: 119,147,890-119,258,448 RN7SL468P, C1QL2, 3 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
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