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Items: 1 to 20 of 234

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974385inversion1nstd209human GRCh38 chr2: 64,078,330-67,334,176 , GRCh37.p13 chr2: 64,305,464-67,561,308 , MEIS1, 63 more genes
    nsv5959003insertion1nstd209human GRCh38 chr2: 65,267,862-65,267,862 , GRCh37.p13 chr2: 65,494,996-65,494,996 ACTR2
    nsv5886697copy number variation1nstd209human GRCh38 chr2: 65,229,697-65,229,746 , GRCh37.p13 chr2: 65,456,831-65,456,880 ACTR2
    nsv5880002copy number variation1nstd209human GRCh38 chr2: 65,248,183-65,248,622 , GRCh37.p13 chr2: 65,475,317-65,475,756 ACTR2
    nsv5868908copy number variation1nstd209human GRCh38 chr2: 65,235,703-65,238,915 , GRCh37.p13 chr2: 65,462,837-65,466,049 ACTR2
    nsv5833782copy number variation1nstd209human GRCh38 chr2: 65,235,524-65,238,423 , GRCh37.p13 chr2: 65,462,658-65,465,557 ACTR2
    nsv5730463mobile element insertion1nstd211human GRCh38 chr2: 65,235,917-65,235,917 , GRCh37.p13 chr2: 65,463,051-65,463,051 ACTR2
    nsv5689191mobile element insertion1nstd211human GRCh38 chr2: 65,267,890-65,267,890 , GRCh37.p13 chr2: 65,495,024-65,495,024 ACTR2
    nsv5622491insertion1nstd207human GRCh38 chr2: 65,234,504-65,234,504 , GRCh37.p13 chr2: 65,461,638-65,461,638 ACTR2
    nsv5614279insertion1nstd207human GRCh38 chr2: 65,238,655-65,238,655 , GRCh37.p13 chr2: 65,465,789-65,465,789 ACTR2
    nsv5562886mobile element insertion1nstd206human GRCh38 chr2: 65,235,931-65,235,968 , GRCh37.p13 chr2: 65,463,065-65,463,102 ACTR2
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5439366copy number variation1nstd206human GRCh38 chr2: 65,235,686-65,238,944 , GRCh37.p13 chr2: 65,462,820-65,466,078 ACTR2
    nsv5297167copy number variation1nstd204human GRCh38.p13 chr2: 65,235,378-65,239,002 , GRCh37.p13 chr2: 65,462,512-65,466,136 ACTR2
    nsv5218223copy number variation1nstd204human GRCh38.p13 chr2: 65,235,724-65,238,423 , GRCh37.p13 chr2: 65,462,858-65,465,557 ACTR2
    nsv5205594copy number variation1nstd204human GRCh38.p13 chr2: 65,233,701-65,238,900 , GRCh37.p13 chr2: 65,460,835-65,466,034 ACTR2
    nsv5076409mobile element insertion1nstd203human GRCh38 chr2: 65,247,184-65,247,201 , GRCh37.p13 chr2: 65,474,318-65,474,335 ACTR2
    nsv5065324mobile element insertion1nstd203human GRCh38 chr2: 65,246,973-65,246,988 , GRCh37.p13 chr2: 65,474,107-65,474,122 ACTR2
    nsv5062905mobile element insertion1nstd203human GRCh38 chr2: 65,267,862-65,267,890 , GRCh37.p13 chr2: 65,494,996-65,495,024 ACTR2
    nsv4908765copy number variation1nstd200human GRCh38 chr2: 65,260,264-65,260,956 , GRCh37.p13 chr2: 65,487,398-65,488,090 ACTR2
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