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Items: 1 to 20 of 203

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094547copy number variation1nstd102humanPathogenic GRCh37 chr15: 62,146,656-64,747,263 , GRCh38.p12 chr15: 61,854,457-64,455,064 C2CD4A, SNX22, 40 more genes
    nsv7063733inversion1nstd229human GRCh38 chr15: 63,479,684-65,571,065 , GRCh37.p13 chr15: 63,771,883-65,863,403 TRIP4, RNU5B-1, 45 more genes
    nsv7058713inversion1nstd229human GRCh38 chr15: 64,026,984-64,154,910 , GRCh37.p13 chr15: 64,319,183-64,447,109 PPIB, SNX1, 3 more genes
    nsv6975693copy number variation1nstd229human GRCh38 chr15: 63,942,232-64,243,600 , GRCh37.p13 chr15: 64,234,431-64,535,799 CSNK1G1, DAPK2, 4 more genes
    nsv6968844copy number variation1nstd229human GRCh38 chr15: 64,141,835-64,147,266 , GRCh37.p13 chr15: 64,434,034-64,439,465 SNX1
    nsv6963105copy number variation1nstd229human GRCh38 chr15: 64,075,301-64,120,600 , GRCh37.p13 chr15: 64,367,500-64,412,799 SNX1, CIAO2A
    nsv6595488inversion1nstd223human GRCh38 chr15: 64,026,983-64,154,909 , GRCh37.p13 chr15: 64,319,182-64,447,108 PPIB, SNX1, 3 more genes
    nsv6583366inversion1nstd223human GRCh38 chr15: 64,125,331-64,126,765 , GRCh37.p13 chr15: 64,417,530-64,418,964 SNX1
    nsv6502608copy number variation1nstd223human GRCh38 chr15: 64,104,491-64,109,654 , GRCh37.p13 chr15: 64,396,690-64,401,853 SNX1
    nsv6501116copy number variation1nstd223human GRCh38 chr15: 64,100,398-64,107,990 , GRCh37.p13 chr15: 64,392,597-64,400,189 SNX1
    nsv6133150copy number variation1nstd213human GRCh37 chr15: 59,870,000-66,270,001 , GRCh38.p12 chr15: 59,577,801-65,977,663 GTF2A2, OAZ2, 115 more genes
    nsv6113311mobile element insertion1nstd186human GRCh37 chr15: 64,411,193-64,411,193 , GRCh38.p12 chr15: 64,118,994-64,118,994 SNX1
    nsv5867046copy number variation1nstd209human GRCh38 chr15: 64,109,130-64,111,704 , GRCh37.p13 chr15: 64,401,329-64,403,903 SNX1
    nsv5703873mobile element insertion2nstd211human GRCh38 chr15: 64,119,009-64,119,009 , GRCh37.p13 chr15: 64,411,208-64,411,208 SNX1
    nsv5647046insertion1nstd207human GRCh38 chr15: 64,118,994-64,118,994 , GRCh37.p13 chr15: 64,411,193-64,411,193 SNX1
    nsv5414096mobile element insertion1nstd206human GRCh38 chr15: 64,118,994-64,118,994 , GRCh37.p13 chr15: 64,411,193-64,411,193 SNX1
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5155173mobile element insertion1nstd203human GRCh38 chr15: 64,131,365-64,131,378 , GRCh37.p13 chr15: 64,423,564-64,423,577 SNX1
    nsv5153603mobile element insertion1nstd203human GRCh38 chr15: 64,119,005-64,119,005 , GRCh37.p13 chr15: 64,411,204-64,411,204 SNX1
    nsv5152609mobile element insertion1nstd203human GRCh38 chr15: 64,118,994-64,119,009 , GRCh37.p13 chr15: 64,411,193-64,411,208 SNX1
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