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Items: 1 to 20 of 161

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093363copy number variation1nstd102humanPathogenic GRCh37 chr6: 820,000-21,700,000 , GRCh38.p12 chr6: 820,000-21,699,769 LOC101928354, CNN3P1, 321 more genes
    nsv7058053inversion1nstd229human GRCh38 chr6: 12,061,960-18,307,388 , GRCh37.p13 chr6: 12,062,193-18,307,619 RNU7-133P, CAP2, 87 more genes
    nsv7052250inversion1nstd229human GRCh38 chr6: 11,964,842-17,051,222 , GRCh37.p13 chr6: 11,965,075-17,051,453 LINC02543, ARPC3P5, 66 more genes
    nsv6792602copy number variation1nstd229human GRCh38 chr6: 16,123,701-16,130,200 , GRCh37.p13 chr6: 16,123,932-16,130,431 MYLIP
    nsv6789164copy number variation1nstd229human GRCh38 chr6: 16,128,633-16,135,051 , GRCh37.p13 chr6: 16,128,864-16,135,282 MYLIP
    nsv6784833copy number variation1nstd229human GRCh38 chr6: 16,120,254-16,128,345 , GRCh37.p13 chr6: 16,120,485-16,128,576 MYLIP
    nsv6636333copy number variation1nstd102humanPathogenic GRCh37 chr6: 12,005,630-22,849,647 , GRCh38.p12 chr6: 12,005,397-22,849,418 SOX4, MDH1P2, 136 more genes
    nsv6565072inversion1nstd223human GRCh38 chr6: 11,964,842-17,051,222 , GRCh37.p13 chr6: 11,965,075-17,051,453 GMPR, LOC105374933, 66 more genes
    nsv6408512copy number variation1nstd223human GRCh38 chr6: 16,114,201-16,240,600 , GRCh37.p13 chr6: 16,114,432-16,240,831 MIR4639, RNU6-1114P, 5 more genes
    nsv6396774copy number variation1nstd223human GRCh38 chr6: 16,120,234-16,128,324 , GRCh37.p13 chr6: 16,120,465-16,128,555 MYLIP
    nsv6135469copy number variation1nstd213human GRCh37 chr6: 11,730,000-19,840,001 , GRCh38.p12 chr6: 11,729,767-19,839,770 EDN1, GMPR, 115 more genes
    nsv5726132mobile element insertion1nstd211human GRCh38 chr6: 16,134,940-16,134,940 , GRCh37.p13 chr6: 16,135,171-16,135,171 MYLIP
    nsv5564204copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr6: 15,523,206-16,146,982 , GRCh38.p12 chr6: 15,522,975-16,146,751 MDH1P2, LINC02543, 8 more genes
    nsv5557247mobile element insertion1nstd206human GRCh38 chr6: 16,134,940-16,134,991 , GRCh37.p13 chr6: 16,135,171-16,135,222 MYLIP
    nsv5179720mobile element insertion1nstd203human GRCh38 chr6: 16,134,926-16,134,940 , GRCh37.p13 chr6: 16,135,157-16,135,171 MYLIP
    nsv5080686mobile element insertion1nstd203human GRCh38 chr6: 16,134,940-16,134,953 , GRCh37.p13 chr6: 16,135,171-16,135,184 MYLIP
    nsv4934455copy number variation1nstd200human GRCh38 chr6: 16,129,960-16,292,983 , GRCh37.p13 chr6: 16,130,191-16,293,214 MIR4639, GMPR, 5 more genes
    nsv4932862copy number variation1nstd200human GRCh38 chr6: 16,120,263-16,128,324 , GRCh37.p13 chr6: 16,120,494-16,128,555 MYLIP
    nsv4828515copy number variation1nstd200human GRCh37 chr6: 16,130,191-16,293,214 , GRCh38.p12 chr6: 16,129,960-16,292,983 MRPL42P2, MYLIP, 5 more genes
    nsv4568628mobile element insertion1nstd166human GRCh37.p13 chr6: 16,135,157-16,135,157 , GRCh38.p12 chr6: 16,134,926-16,134,926 MYLIP
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