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Items: 1 to 20 of 159

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5870019copy number variation1nstd209human GRCh38 chr1: 151,318,147-151,318,440 , GRCh37.p13 chr1: 151,290,623-151,290,916 PI4KB
    nsv5690494mobile element insertion1nstd211human GRCh38 chr1: 151,319,382-151,319,382 , GRCh37.p13 chr1: 151,291,858-151,291,858 PI4KB
    nsv5425467copy number variation1nstd206human GRCh38 chr1: 151,318,420-151,321,663 , GRCh37.p13 chr1: 151,290,896-151,294,139 PI4KB
    nsv5423473copy number variation1nstd206human GRCh38 chr1: 151,302,502-151,303,196 , GRCh37.p13 chr1: 151,274,978-151,275,672 PI4KB
    nsv5396214mobile element insertion1nstd206human GRCh38 chr1: 151,319,382-151,319,433 , GRCh37.p13 chr1: 151,291,858-151,291,909 PI4KB
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5381206copy number variation1nstd102humanUncertain significance GRCh37 chr1: 151,122,490-151,585,008 , GRCh38.p12 chr1: 151,150,014-151,612,532 CGN, ZNF687-AS1, 21 more genes
    nsv5347213translocation1nstd200human GRCh38 chr1: 151,303,196-151,303,196 , GRCh38 chr1: 151,302,502-151,302,502 , GRCh37.p13 chr1: 151,275,672-151,275,672 , GRCh37.p13 chr1: 151,274,978-151,274,978 PI4KB
    nsv5342476translocation1nstd200human GRCh37 chr1: 151,274,978-151,274,978 , GRCh37 chr1: 151,275,672-151,275,672 , GRCh38.p12 chr1: 151,302,502-151,302,502 , GRCh38.p12 chr1: 151,303,196-151,303,196 PI4KB
    nsv5219564copy number variation1nstd204human GRCh38.p13 chr1: 151,301,601-151,394,300 , GRCh37.p13 chr1: 151,274,077-151,366,776 RFX5, RFX5-AS1, 2 more genes
    nsv5209006copy number variation1nstd204human GRCh38.p13 chr1: 151,298,010-151,302,572 , GRCh37.p13 chr1: 151,270,486-151,275,048 PI4KB, RN7SL444P
    nsv5062534mobile element insertion1nstd203human GRCh38 chr1: 151,319,365-151,319,382 , GRCh37.p13 chr1: 151,291,841-151,291,858 PI4KB
    nsv4897375copy number variation1nstd200human GRCh38 chr1: 151,318,208-151,321,794 , GRCh37.p13 chr1: 151,290,684-151,294,270 PI4KB
    nsv4897374copy number variation1nstd200human GRCh38 chr1: 151,315,120-151,315,225 , GRCh37.p13 chr1: 151,287,596-151,287,701 PI4KB
    nsv4894673copy number variation1nstd200human GRCh38 chr1: 151,318,440-151,321,643 , GRCh37.p13 chr1: 151,290,916-151,294,119 PI4KB
    nsv4894672copy number variation1nstd200human GRCh38 chr1: 151,316,642-151,319,026 , GRCh37.p13 chr1: 151,289,118-151,291,502 PI4KB
    nsv4781184copy number variation1nstd200human GRCh37 chr1: 151,290,916-151,294,119 , GRCh38.p12 chr1: 151,318,440-151,321,643 PI4KB
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4712598copy number variation1nstd195human GRCh37 chr1: 151,042,151-151,571,701 , GRCh38.p12 chr1: 151,069,675-151,599,225 PI4KB, PSMD4, 24 more genes
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