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Items: 1 to 20 of 146

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6694651copy number variation1nstd229human GRCh38 chr2: 85,403,057-85,405,784 , GRCh37.p13 chr2: 85,630,180-85,632,907 CAPG
    nsv6681461copy number variation1nstd229human GRCh38 chr2: 85,385,802-85,395,228 , GRCh37.p13 chr2: 85,612,925-85,622,351 CAPG, ELMOD3
    nsv6681244copy number variation1nstd229human GRCh38 chr2: 85,286,438-85,844,313 , GRCh37.p13 chr2: 85,513,561-86,071,436 RETSAT, SH2D6, 30 more genes
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CYP1B1-AS1, LOC107985771, 1649 more genes
    nsv6628354copy number variation1nstd224human GRCh37 chr2: 85,614,974-85,649,757 , GRCh38.p12 chr2: 85,387,851-85,422,634 ELMOD3, CAPG, 2 more genes
    nsv6338206copy number variation1nstd223human GRCh38 chr2: 85,385,802-85,395,228 , GRCh37.p13 chr2: 85,612,925-85,622,351 CAPG, ELMOD3
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 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
    nsv6313890copy number variation1nstd102humanPathogenic GRCh37 chr2: 82,486,900-87,322,042 , GRCh38.p12 chr2: 82,259,776-87,094,919 LOC105374836, LOC105374833, 93 more genes
    nsv6282906insertion1nstd214human GRCh38 chr2: 85,409,356-85,409,356 , GRCh37.p13 chr2: 85,636,479-85,636,479 CAPG
    nsv6156175copy number variation1nstd214human GRCh38 chr2: 85,398,203-85,398,257 , GRCh37.p13 chr2: 85,625,326-85,625,380 CAPG
    nsv6134226copy number variation1nstd213human GRCh37 chr2: 85,629,473-85,673,182 , GRCh38.p12 chr2: 85,402,350-85,446,059 CAPG, SH2D6, 3 more genes
    nsv6134225inversion1nstd213human GRCh38.p12 chr2: 85,347,819-85,393,313 , GRCh37 chr2: 85,574,942-85,620,436 CAPG, RETSAT, 2 more genes
    nsv6134133copy number variation1nstd213human GRCh37 chr2: 85,629,468-85,673,182 , GRCh38.p12 chr2: 85,402,345-85,446,059 CAPG, SH2D6, 3 more genes
    nsv6112750copy number variation1nstd102humanPathogenic GRCh37 chr2: 81,209,244-86,688,030 , GRCh38.p12 chr2: 80,982,120-86,460,907 VAMP8, TMSB10, 86 more genes
    nsv5960788insertion1nstd209human GRCh38 chr2: 85,397,698-85,397,698 , GRCh37.p13 chr2: 85,624,821-85,624,821 CAPG
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5452686copy number variation1nstd206human GRCh38 chr2: 85,406,274-85,406,383 , GRCh37.p13 chr2: 85,633,397-85,633,506 CAPG
    nsv5198989mobile element insertion1nstd203human GRCh38 chr2: 85,413,693-85,413,710 , GRCh37.p13 chr2: 85,640,816-85,640,833 CAPG, LOC105374841
    nsv5065767mobile element insertion1nstd203human GRCh38 chr2: 85,405,245-85,405,256 , GRCh37.p13 chr2: 85,632,368-85,632,379 CAPG
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