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Items: 1 to 20 of 245

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137724copy number variation1nstd102humanPathogenic GRCh37 chr1: 16,785,250-23,491,592 , GRCh38.p12 chr1: 16,458,755-23,165,099 PADI1, RPS15AP6, 176 more genes
    nsv6119969copy number variation1nstd186human GRCh37 chr1: 22,420,791-22,421,089 , GRCh38.p12 chr1: 22,094,298-22,094,596 CDC42
    nsv5977796inversion1nstd209human GRCh38 chr1: 22,029,244-22,112,233 , GRCh37.p13 chr1: 22,355,737-22,438,726 CDC42, LINC00339, 2 more genes
    nsv5885671copy number variation1nstd209human GRCh38 chr1: 22,082,073-22,082,148 , GRCh37.p13 chr1: 22,408,566-22,408,641 CDC42
    nsv5874315copy number variation1nstd209human GRCh38 chr1: 22,094,285-22,094,595 , GRCh37.p13 chr1: 22,420,778-22,421,088 CDC42
    nsv5692166mobile element insertion1nstd211human GRCh38 chr1: 22,098,607-22,098,607 , GRCh37.p13 chr1: 22,425,100-22,425,100 CDC42
    nsv5689791mobile element insertion1nstd211human GRCh38 chr1: 22,055,886-22,055,886 , GRCh37.p13 chr1: 22,382,379-22,382,379 CDC42
    nsv5619349insertion1nstd207human GRCh38 chr1: 22,070,759-22,070,759 , GRCh37.p13 chr1: 22,397,252-22,397,252 CDC42
    nsv5570947copy number variation1nstd207human GRCh38 chr1: 22,094,285-22,094,595 , GRCh37.p13 chr1: 22,420,778-22,421,088 CDC42
    nsv5427686copy number variation1nstd206human GRCh38 chr1: 22,064,395-28,290,354 , GRCh37.p13 chr1: 22,390,888-28,616,865 , NCMAP-DT, 201 more genes
    nsv5426177copy number variation1nstd206human GRCh38 chr1: 22,094,298-22,094,596 , GRCh37.p13 chr1: 22,420,791-22,421,089 CDC42
    nsv5413920copy number variation1nstd206human GRCh38 chr1: 22,089,349-22,089,551 , GRCh37.p13 chr1: 22,415,842-22,416,044 CDC42
    nsv5394507mobile element insertion1nstd206human GRCh38 chr1: 22,098,607-22,098,658 , GRCh37.p13 chr1: 22,425,100-22,425,151 CDC42
    nsv5383496mobile element deletion2nstd186human GRCh37 chr1: 22,420,791-22,421,089 , GRCh38.p12 chr1: 22,094,298-22,094,596 CDC42
    nsv5365457translocation1nstd200human GRCh38 chr1: 21,986,165-21,986,165 , GRCh38 chr1: 22,064,870-22,064,870 , GRCh37.p13 chr1: 22,312,658-22,312,658 , GRCh37.p13 chr1: 22,391,363-22,391,363 CDC42, CELA3B, 2 more genes
    nsv5349573translocation1nstd200human GRCh38 chr1: 22,089,349-22,089,349 , GRCh38 chr1: 22,089,551-22,089,551 , GRCh37.p13 chr1: 22,415,842-22,415,842 , GRCh37.p13 chr1: 22,416,044-22,416,044 CDC42
    nsv5293461copy number variation1nstd204human GRCh38.p13 chr1: 22,076,492-22,076,660 , GRCh37.p13 chr1: 22,402,985-22,403,153 CDC42
    nsv5216375copy number variation1nstd204human GRCh38.p13 chr1: 22,082,472-22,083,571 , GRCh37.p13 chr1: 22,408,965-22,410,064 CDC42
    nsv5205876mobile element deletion1nstd204human GRCh38.p13 chr1: 22,094,268-22,094,618 , GRCh37.p13 chr1: 22,420,761-22,421,111 CDC42
    nsv5203201copy number variation1nstd204human GRCh37.p13 chr1: 22,335,794-22,381,393 , GRCh38.p13 chr1: 22,009,301-22,054,900 CDC42, CELA3A, 5 more genes
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