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Items: 1 to 20 of 284

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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
    nsv7049186inversion1nstd229human GRCh38 chr4: 38,135,041-40,245,309 , GRCh37.p13 chr4: 38,136,662-40,246,929 SMIM14, RNU6-887P, 42 more genes
    nsv7044761inversion1nstd229human GRCh38 chr4: 38,652,543-38,653,462 , GRCh37.p13 chr4: 38,654,164-38,655,083 KLF3-AS1
    nsv7038584inversion1nstd229human GRCh38 chr4: 38,474,718-40,416,508 , GRCh37.p13 chr4: 38,476,339-40,418,525 RPL9, UBE2K, 41 more genes
    nsv6736556copy number variation1nstd229human GRCh38 chr4: 38,629,536-38,632,557 , GRCh37.p13 chr4: 38,631,157-38,634,178 KLF3-AS1
    nsv6729152copy number variation1nstd229human GRCh38 chr4: 38,623,035-38,626,542 , GRCh37.p13 chr4: 38,624,656-38,628,163 KLF3-AS1
    nsv6726948copy number variation1nstd229human GRCh38 chr4: 38,625,243-38,628,596 , GRCh37.p13 chr4: 38,626,864-38,630,217 KLF3-AS1
    nsv6720211copy number variation1nstd229human GRCh38 chr4: 38,662,721-38,662,807 , GRCh37.p13 chr4: 38,664,342-38,664,428 KLF3-AS1, KLF3
    nsv6719125copy number variation1nstd229human GRCh38 chr4: 38,661,210-38,661,241 , GRCh37.p13 chr4: 38,662,831-38,662,862 KLF3-AS1
    nsv6718880copy number variation1nstd229human GRCh38 chr4: 38,639,698-38,639,750 , GRCh37.p13 chr4: 38,641,319-38,641,371 KLF3-AS1
    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
    nsv6567537inversion1nstd223human GRCh38 chr4: 38,654,948-38,655,621 , GRCh37.p13 chr4: 38,656,569-38,657,242 KLF3-AS1
    nsv6567528inversion1nstd223human GRCh38 chr4: 38,651,510-38,651,867 , GRCh37.p13 chr4: 38,653,131-38,653,488 KLF3-AS1
    nsv6564446inversion1nstd223human GRCh38 chr4: 38,618,376-38,618,944 , GRCh37.p13 chr4: 38,619,997-38,620,565 KLF3-AS1
    nsv6560589inversion1nstd223human GRCh38 chr4: 38,649,724-38,650,222 , GRCh37.p13 chr4: 38,651,345-38,651,843 KLF3-AS1
    nsv6560519inversion1nstd223human GRCh38 chr4: 38,655,234-38,655,715 , GRCh37.p13 chr4: 38,656,855-38,657,336 KLF3-AS1
    nsv6394887copy number variation1nstd223human GRCh38 chr4: 38,645,599-38,648,454 , GRCh37.p13 chr4: 38,647,220-38,650,075 KLF3-AS1
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