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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148157copy number variation1nstd102humanPathogenic GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396 OR7E84P, FAM193A, 764 more genes
    nsv6733455copy number variation1nstd229human GRCh38 chr4: 52,712,269-52,714,384 , GRCh37.p13 chr4: 53,578,436-53,580,551 DANCR, MIR4449, 1 more genes
    nsv6732675copy number variation1nstd229human GRCh38 chr4: 52,191,024-52,824,366 , GRCh37.p13 chr4: 53,057,190-53,690,533 LOC107986279, USP46-DT, 9 more genes
    nsv6727947copy number variation1nstd229human GRCh38 chr4: 52,698,577-52,798,901 , GRCh37.p13 chr4: 53,564,744-53,665,068 SNORA26, ERVMER34-1, 4 more genes
    nsv6724910copy number variation1nstd229human GRCh38 chr4: 52,549,568-52,825,492 , GRCh37.p13 chr4: 53,415,734-53,691,659 DANCR, SNORA26, 6 more genes
    nsv6637063copy number variation1nstd102humanUncertain significance GRCh37 chr4: 52,685,980-59,272,025 , GRCh38.p12 chr4: 51,819,814-58,405,859 SPINK2, RN7SL492P, 100 more genes
    nsv6637004copy number variation1nstd102humanUncertain significance GRCh37 chr4: 53,098,544-53,949,065 , GRCh38.p12 chr4: 52,232,378-53,082,898 LINC01618, LOC107986279, 12 more genes
    nsv6636907copy number variation1nstd102humanUncertain significance GRCh37 chr4: 53,434,611-54,079,547 , GRCh38.p12 chr4: 52,568,445-53,213,380 USP46, LOC107986281, 9 more genes
    nsv6629927copy number variation1nstd224human GRCh37 chr4: 53,578,009-53,646,007 , GRCh38.p12 chr4: 52,711,842-52,779,840 MIR4449, LOC107986281, 3 more genes
    nsv6313624copy number variation1nstd102humanUncertain significance GRCh37 chr4: 53,091,609-53,953,124 , GRCh38.p12 chr4: 52,225,443-53,086,957 LOC100419861, RASL11B, 12 more genes
    nsv6313491copy number variation1nstd102humanUncertain significance GRCh37 chr4: 53,435,144-54,091,178 , GRCh38.p12 chr4: 52,568,978-53,225,011 USP46-DT, RASL11B, 9 more genes
    nsv6291432copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354 SNHG27, TNIP3, 1091 more genes
    nsv6291206copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,685,685-58,104,722 , GRCh38.p12 chr4: 51,819,519-57,238,556 SRD5A3, DCUN1D4, 96 more genes
    nsv5674237copy number variation1nstd102humanPathogenic GRCh38 chr4: 51,891,814-76,009,719 , GRCh37.p13 chr4: 52,757,980-76,930,872 FTLP10, RNU6-410P, 335 more genes
    nsv5341397translocation1nstd200human GRCh37 chr4: 53,580,032-53,580,032 , GRCh37 chr22: 17,714,953-17,714,953 , GRCh38.p12 chr22: 17,234,063-17,234,063 , GRCh38.p12 chr4: 52,713,865-52,713,865 DANCR, SNORA26
    nsv5039232inversion1nstd200human GRCh38 chr4: 9,660,225-57,055,279 , GRCh37.p13 chr4: 9,661,849-57,921,445 , KRT18P63, 533 more genes
    nsv5034204inversion1nstd200human GRCh38 chr4: 45,103,677-117,623,076 , GRCh37.p13 chr4: 45,105,694-118,544,231 , LOC100129728, 913 more genes
    nsv4878267inversion1nstd200human GRCh37 chr4: 45,105,694-118,544,231 , GRCh38.p12 chr4: 45,103,677-117,623,076 , MIR367, 913 more genes
    nsv4791811copy number variation1nstd200human GRCh37 chr4: 53,578,843-53,584,262 , GRCh38.p12 chr4: 52,712,676-52,718,095 MIR4449, DANCR, 1 more genes
    nsv4761770inversion1nstd199human GRCh37 chr4: 34,988-191,015,248 , GRCh38.p12 chr4: 34,988-190,094,093 , ADD1, 2433 more genes
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