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Items: 1 to 20 of 123

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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
    nsv7056117inversion1nstd229human GRCh38 chr6: 16,000,248-16,036,547 , GRCh37.p13 chr6: 16,000,479-16,036,778 LINC02543
    nsv7052250inversion1nstd229human GRCh38 chr6: 11,964,842-17,051,222 , GRCh37.p13 chr6: 11,965,075-17,051,453 LINC02543, ARPC3P5, 66 more genes
    nsv6791050copy number variation1nstd229human GRCh38 chr6: 15,996,738-16,000,018 , GRCh37.p13 chr6: 15,996,969-16,000,249 LINC02543
    nsv6790204copy number variation1nstd229human GRCh38 chr6: 16,000,401-16,107,200 , GRCh37.p13 chr6: 16,000,632-16,107,431 MDH1P2, LINC02543
    nsv6781790copy number variation1nstd229human GRCh38 chr6: 15,965,034-16,056,334 , GRCh37.p13 chr6: 15,965,265-16,056,565 LOC105374949, LINC02543
    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
    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
    nsv5689802mobile element insertion1nstd211human GRCh38 chr6: 15,995,650-15,995,650 , GRCh37.p13 chr6: 15,995,881-15,995,881 LINC02543
    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
    nsv5464122copy number variation1nstd206human GRCh38 chr6: 15,998,331-15,998,398 , GRCh37.p13 chr6: 15,998,562-15,998,629 LINC02543
    nsv5397408mobile element insertion1nstd206human GRCh38 chr6: 15,995,650-15,995,701 , GRCh37.p13 chr6: 15,995,881-15,995,932 LINC02543
    nsv4729080copy number variation1nstd102humanUncertain significance GRCh37 chr6: 14,590,996-16,067,315 , GRCh38.p12 chr6: 14,590,765-16,067,084 LOC105374946, LOC105374949, 16 more genes
    nsv4457139copy number variation1nstd102humanUncertain significance GRCh37 chr6: 14,715,955-17,223,929 , GRCh38.p12 chr6: 14,715,724-17,223,698 MDH1P2, ATXN1, 28 more genes
    nsv4456780copy number variation1nstd102humanPathogenic GRCh37 chr6: 156,974-23,221,621 , GRCh38.p12 chr6: 156,974-23,221,393 LOC105374960, LOC101928573, 342 more genes
    nsv4456299copy number variation1nstd102humanPathogenic GRCh37 chr6: 13,910,125-22,000,204 , GRCh38.p12 chr6: 13,909,894-21,999,975 LOC101928354, MBOAT1, 101 more genes
    nsv4455888copy number variation1nstd102humanUncertain significance GRCh37 chr6: 13,248,587-18,083,552 , GRCh38.p12 chr6: 13,248,355-18,083,321 RNU6-522P, LOC105374942, 70 more genes
    nsv3922769copy number variation1nstd102humanUncertain significance NCBI36 chr6: 14,653,555-16,171,002 , GRCh38 chr6: 14,545,345-16,062,792 , GRCh37 chr6: 14,545,576-16,063,023 ARPC3P5, RNU6-522P, 16 more genes
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