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Items: 1 to 20 of 428

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5970570insertion1nstd209human GRCh38 chr14: 100,026,381-100,026,381 , GRCh37.p13 chr14: 100,492,718-100,492,718 EVL
    nsv5939359copy number variation1nstd209human GRCh38 chr14: 100,056,097-100,056,314 , GRCh37.p13 chr14: 100,522,434-100,522,651 EVL
    nsv5928125copy number variation1nstd209human GRCh38 chr14: 100,013,046-100,013,118 , GRCh37.p13 chr14: 100,479,383-100,479,455 EVL
    nsv5714875mobile element insertion1nstd211human GRCh38 chr14: 100,029,035-100,029,035 , GRCh37.p13 chr14: 100,495,372-100,495,372 EVL
    nsv5709785mobile element insertion2nstd211human GRCh38 chr14: 100,026,394-100,026,394 , GRCh37.p13 chr14: 100,492,731-100,492,731 EVL
    nsv5698002mobile element insertion2nstd211human GRCh38 chr14: 100,047,145-100,047,145 , GRCh37.p13 chr14: 100,513,482-100,513,482 EVL
    nsv5695913mobile element insertion1nstd211human GRCh38 chr14: 100,060,971-100,060,971 , GRCh37.p13 chr14: 100,527,308-100,527,308 EVL
    nsv5650024insertion1nstd207human GRCh38 chr14: 100,026,381-100,026,381 , GRCh37.p13 chr14: 100,492,718-100,492,718 EVL
    nsv5563470mobile element insertion1nstd206human GRCh38 chr14: 100,029,035-100,029,086 , GRCh37.p13 chr14: 100,495,372-100,495,423 EVL
    nsv5538763insertion1nstd206human GRCh38 chr14: 100,026,381-100,026,381 , GRCh37.p13 chr14: 100,492,718-100,492,718 EVL
    nsv5510775copy number variation1nstd206human GRCh38 chr14: 99,983,838-99,990,591 , GRCh37.p13 chr14: 100,450,175-100,456,928 EVL
    nsv5505019copy number variation1nstd206human GRCh38 chr14: 100,101,567-100,102,984 , GRCh37.p13 chr14: 100,567,904-100,569,321 EVL
    nsv5502140copy number variation1nstd206human GRCh38 chr14: 100,056,097-100,056,315 , GRCh37.p13 chr14: 100,522,434-100,522,652 EVL
    nsv5500182copy number variation1nstd206human GRCh38 chr14: 100,104,331-100,104,880 , GRCh37.p13 chr14: 100,570,668-100,571,217 EVL
    nsv5498590copy number variation1nstd206human GRCh38 chr14: 80,522,636-106,763,637 , GRCh37.p13 chr14: 80,988,980-106,929,356 , RPS18P2, 713 more genes
    nsv5497157copy number variation1nstd206human GRCh38 chr14: 100,114,684-100,114,841 , GRCh37.p13 chr14: 100,581,021-100,581,178 EVL
    nsv5357602translocation1nstd200human GRCh38 chr14: 100,104,880-100,104,880 , GRCh38 chr14: 100,104,331-100,104,331 , GRCh37.p13 chr14: 100,571,217-100,571,217 , GRCh37.p13 chr14: 100,570,668-100,570,668 EVL
    nsv5357600translocation1nstd200human GRCh38 chr14: 100,056,315-100,056,315 , GRCh38 chr14: 100,056,097-100,056,097 , GRCh37.p13 chr14: 100,522,434-100,522,434 , GRCh37.p13 chr14: 100,522,652-100,522,652 EVL
    nsv5357599translocation1nstd200human GRCh38 chr14: 100,030,651-100,030,651 , GRCh38 chr20: 13,642,732-13,642,732 , GRCh37.p13 chr14: 100,496,988-100,496,988 , GRCh37.p13 chr20: 13,623,379-13,623,379 EVL
    nsv5343181translocation1nstd200human GRCh37 chr14: 100,522,434-100,522,434 , GRCh37 chr14: 100,522,652-100,522,652 , GRCh38.p12 chr14: 100,056,097-100,056,097 , GRCh38.p12 chr14: 100,056,315-100,056,315 EVL
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