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Items: 1 to 20 of 186

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7049504inversion1nstd229human GRCh38 chr2: 100,567,128-100,571,579 , GRCh37.p13 chr2: 101,183,590-101,188,041 PDCL3
    nsv6696353copy number variation1nstd229human GRCh38 chr2: 100,567,590-100,578,564 , GRCh37.p13 chr2: 101,184,052-101,195,026 PDCL3
    nsv6693761copy number variation1nstd229human GRCh38 chr2: 100,556,064-100,568,501 , GRCh37.p13 chr2: 101,172,526-101,184,963 PDCL3
    nsv6692419copy number variation1nstd229human GRCh38 chr2: 100,561,334-100,576,048 , GRCh37.p13 chr2: 101,177,796-101,192,510 PDCL3
    nsv6688925copy number variation1nstd229human GRCh38 chr2: 100,463,418-100,750,618 , GRCh37.p13 chr2: 101,079,880-101,367,080 NANOGNBP1, LINC01849, 9 more genes
    nsv6688258copy number variation1nstd229human GRCh38 chr2: 100,568,316-100,568,357 , GRCh37.p13 chr2: 101,184,778-101,184,819 PDCL3
    nsv6684550copy number variation1nstd229human GRCh38 chr2: 100,503,504-100,628,510 , GRCh37.p13 chr2: 101,119,966-101,244,972 LINC01849, PDCL3, 2 more genes
    nsv6683101copy number variation1nstd229human GRCh38 chr2: 100,111,642-100,877,626 , GRCh37.p13 chr2: 100,728,104-101,494,088 CHST10, CYCSP7, 16 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
    nsv6349371copy number variation1nstd223human GRCh38 chr2: 100,577,491-100,579,859 , GRCh37.p13 chr2: 101,193,953-101,196,321 PDCL3
    nsv6345270copy number variation1nstd223human GRCh38 chr2: 100,570,666-100,571,237 , GRCh37.p13 chr2: 101,187,128-101,187,699 PDCL3
    nsv6344266copy number variation1nstd223human GRCh38 chr2: 100,561,355-100,576,007 , GRCh37.p13 chr2: 101,177,817-101,192,469 PDCL3
    nsv6343808copy number variation1nstd223human GRCh38 chr2: 100,567,590-100,578,559 , GRCh37.p13 chr2: 101,184,052-101,195,021 PDCL3
    nsv6336189copy number variation1nstd223human GRCh38 chr2: 100,575,301-100,576,200 , GRCh37.p13 chr2: 101,191,763-101,192,662 PDCL3
    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
    nsv6134134copy number variation1nstd213human GRCh37 chr2: 101,130,000-101,230,001 , GRCh38.p12 chr2: 100,513,538-100,613,539 PDCL3, HMGN2P22, 1 more genes
    nsv5869967copy number variation1nstd209human GRCh38 chr2: 100,572,304-100,572,609 , GRCh37.p13 chr2: 101,188,766-101,189,071 PDCL3
    nsv5721961mobile element insertion1nstd211human GRCh38 chr2: 100,576,352-100,576,352 , GRCh37.p13 chr2: 101,192,814-101,192,814 PDCL3
    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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