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Items: 1 to 20 of 221

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7050876inversion1nstd229human GRCh38 chr2: 64,242,234-64,242,285 , GRCh37.p13 chr2: 64,469,368-64,469,419 LOC100507006
    nsv6677642copy number variation1nstd229human GRCh38 chr2: 64,241,201-64,268,400 , GRCh37.p13 chr2: 64,468,335-64,495,534 LOC100507006
    nsv6676581copy number variation1nstd229human GRCh38 chr2: 63,840,693-64,286,247 , GRCh37.p13 chr2: 64,067,827-64,513,381 LINC00309, UGP2, 3 more genes
    nsv6671434copy number variation1nstd229human GRCh38 chr2: 64,150,059-64,514,853 , GRCh37.p13 chr2: 64,377,193-64,741,987 LGALSL-DT, LINC01805, 8 more genes
    nsv6668073copy number variation1nstd229human GRCh38 chr2: 64,115,004-64,288,383 , GRCh37.p13 chr2: 64,342,138-64,515,517 LOC100507006, LINC00309, 1 more genes
    nsv6661490copy number variation1nstd229human GRCh38 chr2: 64,210,609-64,960,847 , GRCh37.p13 chr2: 64,437,743-65,187,981 RN7SL211P, RNU6-100P, 23 more genes
    nsv6660243copy number variation1nstd229human GRCh38 chr2: 64,242,823-64,418,457 , GRCh37.p13 chr2: 64,469,957-64,645,591 RPL23AP37, LOC105374769, 5 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
    nsv6628331copy number variation1nstd224human GRCh37 chr2: 64,342,469-64,517,459 , GRCh38.p12 chr2: 64,115,335-64,290,325 LOC100507006, PELI1, 1 more genes
    nsv6551094inversion1nstd223human GRCh38 chr2: 64,078,330-67,334,177 , GRCh37.p13 chr2: 64,305,464-67,561,309 LINC01805, LINC02579, 59 more genes
    nsv6544527inversion1nstd223human GRCh38 chr2: 64,236,321-64,236,971 , GRCh37.p13 chr2: 64,463,455-64,464,105 LOC100507006
    nsv6352326copy number variation1nstd223human GRCh38 chr2: 64,252,559-64,257,387 , GRCh37.p13 chr2: 64,479,693-64,484,521 LOC100507006
    nsv6352218copy number variation1nstd223human GRCh38 chr2: 64,248,001-64,297,100 , GRCh37.p13 chr2: 64,475,135-64,524,234 LOC100507006
    nsv6348273copy number variation1nstd223human GRCh38 chr2: 64,248,201-64,255,600 , GRCh37.p13 chr2: 64,475,335-64,482,734 LOC100507006
    nsv6345662copy number variation1nstd223human GRCh38 chr2: 64,179,701-64,298,300 , GRCh37.p13 chr2: 64,406,835-64,525,434 LINC00309, LOC100507006, 1 more genes
    nsv6343721copy number variation1nstd223human GRCh38 chr2: 64,252,101-64,256,300 , GRCh37.p13 chr2: 64,479,235-64,483,434 LOC100507006
    nsv6341869copy number variation1nstd223human GRCh38 chr2: 64,234,401-64,236,700 , GRCh37.p13 chr2: 64,461,535-64,463,834 LOC100507006
    nsv6338649copy number variation1nstd223human GRCh38 chr2: 64,115,004-64,288,381 , GRCh37.p13 chr2: 64,342,138-64,515,515 PELI1, LINC00309, 1 more genes
    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
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