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Items: 1 to 20 of 145

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148229copy number variation1nstd102humanPathogenic GRCh38 chr4: 2,904,667-42,963,232 , GRCh37.p13 chr4: 2,906,394-42,965,249 LINC01587, RN7SKP82, 509 more genes
    nsv7148161copy number variation1nstd102humanPathogenic GRCh38 chr4: 1-49,062,177 , GRCh37.p13 chr4: 507,005-49,064,194 SLIRPP2, STIM2-AS1, 659 more genes
    nsv7148157copy number variation1nstd102humanPathogenic GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396 OR7E84P, FAM193A, 764 more genes
    nsv7096849copy number variation1nstd102humanUncertain significance GRCh37 chr4: 38,765,721-39,478,735 , GRCh38.p12 chr4: 38,764,100-39,477,115 TMEM156, TLR6, 14 more genes
    nsv7049186inversion1nstd229human GRCh38 chr4: 38,135,041-40,245,309 , GRCh37.p13 chr4: 38,136,662-40,246,929 SMIM14, RNU6-887P, 42 more genes
    nsv7038584inversion1nstd229human GRCh38 chr4: 38,474,718-40,416,508 , GRCh37.p13 chr4: 38,476,339-40,418,525 RPL9, UBE2K, 41 more genes
    nsv6737735copy number variation1nstd229human GRCh38 chr4: 38,785,961-38,791,330 , GRCh37.p13 chr4: 38,787,582-38,792,951 TLR1
    nsv6720334copy number variation1nstd229human GRCh38 chr4: 38,712,201-38,790,500 , GRCh37.p13 chr4: 38,713,822-38,792,121 TLR1, RNA5SP158, 2 more genes
    nsv6720085copy number variation1nstd229human GRCh38 chr4: 38,701,501-39,003,800 , GRCh37.p13 chr4: 38,703,122-39,005,420 TLR1, LOC105374413, 7 more genes
    nsv6636898copy number variation1nstd102humanUncertain significance GRCh37 chr4: 38,589,565-38,926,476 , GRCh38.p12 chr4: 38,587,944-38,924,855 TLR10, MIR574, 7 more genes
    nsv6634358copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-49,089,361 , GRCh38.p12 chr4: 68,453-49,087,344 LINC02475, LOC105374344, 658 more genes
    nsv6629863copy number variation1nstd224human GRCh37 chr4: 38,799,162-38,829,111 , GRCh38.p12 chr4: 38,797,541-38,827,490 TLR1, TLR6
    nsv6387241copy number variation1nstd223human GRCh38 chr4: 38,800,701-38,839,500 , GRCh37.p13 chr4: 38,802,322-38,841,121 TLR6, TLR1
    nsv6386068copy number variation1nstd223human GRCh38 chr4: 38,790,832-38,791,247 , GRCh37.p13 chr4: 38,792,453-38,792,868 TLR1
    nsv6380603copy number variation1nstd223human GRCh38 chr4: 38,796,089-38,798,462 , GRCh37.p13 chr4: 38,797,710-38,800,083 TLR1
    nsv6315440copy number variation1nstd102humanPathogenic GRCh37 chr4: 114,784-47,569,569 , GRCh38.p12 chr4: 114,902-47,567,552 FAM86KP, ENPP7P11, 631 more genes
    nsv6312251copy number variation1nstd102humanUncertain significance GRCh37 chr4: 38,765,721-41,750,627 , GRCh38.p12 chr4: 38,764,100-41,748,610 RNU6-32P, SMIM14-DT, 52 more genes
    nsv6296852copy number variation1nstd186human GRCh37 chr4: 38,798,621-38,829,621 , GRCh38.p12 chr4: 38,797,000-38,828,000 TLR6, TLR1
    nsv6243979mobile element insertion1nstd215human GRCh38 chr4: 38,802,301-38,802,301 , GRCh37.p13 chr4: 38,803,922-38,803,922 TLR1
    nsv6243978mobile element insertion1nstd215human GRCh38 chr4: 38,798,692-38,798,692 , GRCh37.p13 chr4: 38,800,313-38,800,313 TLR1
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