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Items: 1 to 20 of 207

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137788copy number variation1nstd102humanPathogenic GRCh37 chr2: 24,601,818-43,466,284 , GRCh38.p12 chr2: 24,378,949-43,239,145 GTF3C2-AS1, MAPRE3-AS1, 316 more genes
    nsv6112680copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 24,881,528-43,460,021 , GRCh38.p12 chr2: 24,658,659-43,232,882 ADCY3, ALK, 314 more genes
    nsv5683676mobile element insertion2nstd211human GRCh38 chr2: 37,191,058-37,191,058 , GRCh37.p13 chr2: 37,418,201-37,418,201 SULT6B1
    nsv5621306insertion1nstd207human GRCh38 chr2: 37,166,500-37,166,500 , GRCh37.p13 chr2: 37,393,643-37,393,643 SULT6B1
    nsv5610902insertion1nstd207human GRCh38 chr2: 37,166,540-37,166,540 , GRCh37.p13 chr2: 37,393,683-37,393,683 SULT6B1
    nsv5450123copy number variation1nstd206human GRCh38 chr2: 37,174,210-37,176,309 , GRCh37.p13 chr2: 37,401,353-37,403,452 SULT6B1
    nsv5438523copy number variation1nstd206human GRCh38 chr2: 37,170,982-37,171,930 , GRCh37.p13 chr2: 37,398,125-37,399,073 SULT6B1
    nsv5411539mobile element insertion1nstd206human GRCh38 chr2: 37,191,058-37,191,109 , GRCh37.p13 chr2: 37,418,201-37,418,252 SULT6B1
    nsv5296215copy number variation1nstd204human GRCh38.p13 chr2: 37,087,219-37,302,265 , GRCh37.p13 chr2: 37,314,362-37,529,408 EIF2AK2, CEBPZ, 7 more genes
    nsv5287365copy number variation1nstd204human GRCh37.p13 chr2: 37,290,015-37,405,346 , GRCh38.p13 chr2: 37,062,872-37,178,203 EIF2AK2, HEATR5B, 3 more genes
    nsv5209726copy number variation1nstd204human GRCh38.p13 chr2: 37,172,607-37,173,606 , GRCh37.p13 chr2: 37,399,750-37,400,749 SULT6B1
    nsv5208220copy number variation1nstd204human GRCh37.p13 chr2: 37,369,969-37,434,572 , GRCh38.p13 chr2: 37,142,826-37,207,429 EIF2AK2, CEBPZ, 4 more genes
    nsv5206320copy number variation1nstd204human GRCh37.p13 chr2: 37,314,444-37,529,243 , GRCh38.p13 chr2: 37,087,301-37,302,100 EIF2AK2, CEBPZ, 7 more genes
    nsv5204132copy number variation1nstd204human GRCh38.p13 chr2: 37,062,901-37,178,100 , GRCh37.p13 chr2: 37,290,044-37,405,243 SULT6B1, EIF2AK2, 3 more genes
    nsv4901211copy number variation1nstd200human GRCh38 chr2: 37,174,354-37,174,431 , GRCh37.p13 chr2: 37,401,497-37,401,574 SULT6B1
    nsv4901210copy number variation1nstd200human GRCh38 chr2: 37,173,141-37,178,179 , GRCh37.p13 chr2: 37,400,284-37,405,322 SULT6B1
    nsv4901207copy number variation1nstd200human GRCh38 chr2: 37,062,882-37,178,202 , GRCh37.p13 chr2: 37,290,025-37,405,345 HEATR5B, GPATCH11, 3 more genes
    nsv4776161copy number variation1nstd200human GRCh37 chr2: 37,290,025-37,405,345 , GRCh38.p12 chr2: 37,062,882-37,178,202 GPATCH11, HEATR5B, 3 more genes
    nsv4733025copy number variation1nstd199human GRCh37 chr2: 37,393,574-37,393,640 , GRCh38.p12 chr2: 37,166,431-37,166,497 SULT6B1
    nsv4728619copy number variation1nstd102humanUncertain significance GRCh37 chr2: 36,432,453-38,182,274 , GRCh38.p12 chr2: 36,205,310-37,955,131 CDC42EP3, NDUFAF7, 30 more genes
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