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Items: 1 to 20 of 112

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5943185copy number variation1nstd209human GRCh38 chr16: 11,834,364-11,851,581 , GRCh37.p13 chr16: 11,928,221-11,945,438 RSL1D1-DT, RSL1D1
    nsv5877432copy number variation1nstd209human GRCh38 chr16: 11,834,330-11,849,106 , GRCh37.p13 chr16: 11,928,187-11,942,963 RSL1D1
    nsv5656435insertion1nstd207human GRCh38 chr16: 11,837,376-11,837,376 , GRCh37.p13 chr16: 11,931,233-11,931,233 RSL1D1
    nsv5528908copy number variation1nstd206human GRCh38 chr16: 11,850,804-11,856,133 , GRCh37.p13 chr16: 11,944,661-11,949,990 RSL1D1, RSL1D1-DT
    nsv5516789copy number variation1nstd206human GRCh38 chr16: 11,821,307-11,860,154 , GRCh37.p13 chr16: 11,915,164-11,954,011 RSL1D1, BCAR4, 1 more genes
    nsv5515561copy number variation1nstd206human GRCh38 chr16: 11,837,376-11,837,429 , GRCh37.p13 chr16: 11,931,233-11,931,286 RSL1D1
    nsv5277651copy number variation1nstd204human GRCh38.p13 chr16: 11,499,101-11,940,700 , GRCh37.p13 chr16: 11,592,957-12,034,557 , GSPT1, 11 more genes
    nsv5269216copy number variation1nstd204human GRCh38.p13 chr16: 11,821,486-11,841,537 , GRCh37.p13 chr16: 11,915,343-11,935,394 BCAR4, RSL1D1
    nsv5260505copy number variation1nstd204human GRCh38.p13 chr16: 11,821,501-11,859,900 , GRCh37.p13 chr16: 11,915,358-11,953,757 RSL1D1-DT, RSL1D1, 1 more genes
    nsv4994463copy number variation1nstd200human GRCh38 chr16: 11,848,720-11,856,508 , GRCh37.p13 chr16: 11,942,577-11,950,365 RSL1D1, RSL1D1-DT
    nsv4994461copy number variation1nstd200human GRCh38 chr16: 11,821,131-11,865,401 , GRCh37.p13 chr16: 11,914,988-11,959,258 RSL1D1-DT, BCAR4, 1 more genes
    nsv4992754copy number variation1nstd200human GRCh38 chr16: 11,843,714-11,855,298 , GRCh37.p13 chr16: 11,937,571-11,949,155 RSL1D1, RSL1D1-DT
    nsv4729901copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,959,279-30,190,593 , GRCh38.p12 chr16: 2,909,278-30,179,272 NPIPB9, TMEM219, 597 more genes
    nsv4685985copy number variation1nstd102humanPathogenic GRCh37 chr16: 5,805,001-34,230,001 , GRCh38.p12 chr16: 5,755,000-34,995,630 LOC105371069, PKD1P6-NPIPP1, 654 more genes
    nsv4640326copy number variation1nstd186human GRCh37 chr16: 11,931,233-11,931,286 , GRCh38.p12 chr16: 11,837,376-11,837,429 RSL1D1
    nsv4553416insertion1nstd166human GRCh37.p13 chr16: 11,931,215-11,931,215 , GRCh38.p12 chr16: 11,837,358-11,837,358 RSL1D1
    nsv4551612insertion1nstd166human GRCh37.p13 chr16: 11,931,233-11,931,233 , GRCh38.p12 chr16: 11,837,376-11,837,376 RSL1D1
    nsv4540095insertion1nstd166human GRCh37.p13 chr16: 11,931,183-11,931,183 , GRCh38.p12 chr16: 11,837,326-11,837,326 RSL1D1
    nsv4531654copy number variation1nstd166human GRCh37.p13 chr16: 11,931,233-11,931,286 , GRCh38.p12 chr16: 11,837,376-11,837,429 RSL1D1
    nsv4499888mobile element insertion1nstd166human GRCh37.p13 chr16: 11,929,996-11,929,996 , GRCh38.p12 chr16: 11,836,139-11,836,139 RSL1D1
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