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Items: 1 to 20 of 292

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137706copy number variation3nstd102humanPathogenic, Uncertain significance, Likely pathogenic GRCh37 chr15: 22,770,421-23,282,799 , GRCh38.p12 chr15: 22,590,297-23,102,647 CYFIP1, NIPA2, 14 more genes
    nsv6130649insertion1nstd186human GRCh37 chr15: 22,997,178-22,997,180 , GRCh38.p12 chr15: 22,875,888-22,875,890 CYFIP1
    nsv6129815insertion1nstd186human GRCh37 chr15: 22,909,567-22,909,622 , GRCh38.p12 chr15: 22,963,446-22,963,501 , GRCh38.p12 chr15|NT_187603.1: 60,499-60,547 CYFIP1
    nsv6114852mobile element insertion1nstd186human GRCh37 chr15: 22,896,440-22,896,469 , GRCh38.p12 chr15: 22,976,599-22,976,628 , GRCh38.p12 chr15|NT_187603.1: 73,606-73,635 CYFIP1
    nsv6112775copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,833,525-23,264,865 , GRCh38.p12 chr15: 22,608,231-23,039,543 PDCD6IPP1, LOC101927846, 12 more genes
    nsv5980453copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 22,746,948-23,323,445 , GRCh38.p12 chr15: 22,549,651-23,126,120 CYFIP1, NIPA2, 17 more genes
    nsv5972702insertion1nstd209human GRCh38 chr15: 22,875,888-22,875,888 , GRCh37.p13 chr15: 22,997,180-22,997,180 CYFIP1
    nsv5940779copy number variation1nstd209human GRCh38 chr15: 22,967,716-22,967,782 , GRCh37.p13 chr15: 22,905,286-22,905,352 CYFIP1
    nsv5940369copy number variation1nstd209human GRCh38 chr15: 22,963,494-22,963,545 , GRCh37.p13 chr15: 22,909,523-22,909,574 CYFIP1
    nsv5934141copy number variation1nstd209human GRCh38 chr15: 22,890,630-22,890,812 , GRCh37.p13 chr15: 22,982,256-22,982,438 CYFIP1
    nsv5932280copy number variation1nstd209human GRCh38 chr15: 22,883,892-22,886,043 , GRCh37.p13 chr15: 22,987,025-22,989,176 CYFIP1
    nsv5928331copy number variation1nstd209human GRCh38 chr15: 22,774,698-23,445,470 , GRCh37.p13 chr15: 22,646,194-23,098,370 HERC2P6, RN7SL536P, 25 more genes
    nsv5857843copy number variation2nstd209human GRCh38 chr15: 22,951,440-22,955,050 , GRCh37.p13 chr15: 22,918,018-22,921,628 CYFIP1
    nsv5856832copy number variation2nstd209human GRCh38 chr15: 22,963,782-22,966,811 , GRCh37.p13 chr15: 22,906,257-22,909,286 CYFIP1
    nsv5712474mobile element insertion1nstd211human GRCh38 chr15: 22,964,027-22,964,027 , GRCh37.p13 chr15: 22,909,041-22,909,041 CYFIP1
    nsv5712438mobile element insertion1nstd211human GRCh38 chr15: 22,951,300-22,951,300 , GRCh37.p13 chr15: 22,921,768-22,921,768 CYFIP1
    nsv5709035mobile element insertion1nstd211human GRCh38 chr15: 22,976,577-22,976,577 , GRCh37.p13 chr15: 22,896,491-22,896,491 CYFIP1
    nsv5706716mobile element insertion1nstd211human GRCh38 chr15: 22,866,120-22,866,120 , GRCh37.p13 chr15: 23,006,948-23,006,948 CYFIP1, NIPA2
    nsv5672660copy number variation1nstd102humanPathogenic GRCh38 chr15: 22,804,175-30,375,696 , GRCh37.p13 chr15: 23,564,855-30,667,899 TUBBP8, LOC102723564, 218 more genes
    nsv5661654insertion1nstd207human GRCh38 chr15: 22,890,630-22,890,630 , GRCh37.p13 chr15: 22,982,438-22,982,438 CYFIP1
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