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Items: 1 to 20 of 393

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148195copy number variation1nstd102humanPathogenic GRCh37 chr18: 63,476,940-77,960,815 , GRCh38.p12 chr18: 65,809,704-80,202,932 LOC105372202, LINC01896, 149 more genes
    nsv7071884inversion1nstd229human GRCh38 chr18: 66,637,554-68,462,954 , GRCh37.p13 chr18: 64,304,791-66,130,191 LINC01912, AKR1B10P2, 12 more genes
    nsv7069303inversion1nstd229human GRCh38 chr18: 66,516,237-71,816,578 , GRCh37.p13 chr18: 64,183,474-69,483,814 LOC100421257, LINC01899, 48 more genes
    nsv7067725inversion1nstd229human GRCh38 chr18: 63,817,377-68,462,605 , GRCh37.p13 chr18: 61,484,611-66,129,842 LOC105372167, SERPINB10, 32 more genes
    nsv7066376inversion1nstd229human GRCh38 chr18: 61,808,565-71,004,929 , GRCh37.p13 chr18: 59,475,798-68,672,165 DSEL-AS1, LOC112268209, 84 more genes
    nsv7065377inversion1nstd229human GRCh38 chr18: 63,349,981-69,905,763 , GRCh37.p13 chr18: 61,017,214-67,572,999 LOC105372170, CD226, 55 more genes
    nsv7061093inversion1nstd229human GRCh38 chr18: 64,976,437-68,365,978 , GRCh37.p13 chr18: 62,643,673-66,033,215 LOC100129135, LOC105372169, 19 more genes
    nsv7059846inversion1nstd229human GRCh38 chr18: 63,368,950-69,432,892 , GRCh37.p13 chr18: 61,036,183-67,100,128 SERPINB5, SERPINB8, 51 more genes
    nsv7059464inversion1nstd229human GRCh38 chr18: 66,619,106-71,816,572 , GRCh37.p13 chr18: 64,286,343-69,483,808 LIVAR, LOC107985138, 47 more genes
    nsv7016743copy number variation1nstd229human GRCh38 chr18: 67,395,919-67,783,788 , GRCh37.p13 chr18: 65,063,156-65,451,025 LOC105372172, FAM32DP, 4 more genes
    nsv7012514copy number variation1nstd229human GRCh38 chr18: 67,210,350-68,285,675 , GRCh37.p13 chr18: 64,877,587-65,952,912 LOC100129135, LOC105372172, 8 more genes
    nsv7006945copy number variation1nstd229human GRCh38 chr18: 66,759,301-68,790,800 , GRCh37.p13 chr18: 64,426,538-66,458,037 DSEL-AS1, MTL3P, 15 more genes
    nsv7005883copy number variation1nstd229human GRCh38 chr18: 67,083,701-68,358,832 , GRCh37.p13 chr18: 64,750,938-66,026,069 LOC100129135, FAM32DP, 9 more genes
    nsv7005666copy number variation1nstd229human GRCh38 chr18: 67,143,533-67,551,977 , GRCh37.p13 chr18: 64,810,770-65,219,214 DSEL, DSEL-AS1
    nsv7004971copy number variation1nstd229human GRCh38 chr18: 67,454,882-67,539,614 , GRCh37.p13 chr18: 65,122,119-65,206,851 DSEL-AS1, DSEL
    nsv6999939copy number variation1nstd229human GRCh38 chr18: 66,504,332-68,638,093 , GRCh37.p13 chr18: 64,171,569-66,305,330 CDH19, MIR5011, 14 more genes
    nsv6638004copy number variation1nstd102humanPathogenic GRCh37 chr18: 61,520,071-78,014,123 , GRCh38.p12 chr18: 63,852,837-80,256,240 LOC107985151, CD226, 165 more genes
    nsv6638001copy number variation1nstd102humanUncertain significance GRCh37 chr18: 64,432,327-66,522,571 , GRCh38.p12 chr18: 66,765,090-68,855,334 RNU6-1037P, DSEL, 15 more genes
    nsv6637731copy number variation1nstd102humanUncertain significance GRCh37 chr18: 63,826,068-67,913,864 , GRCh38.p12 chr18: 66,158,832-70,246,628 LOC105372180, LOC105372174, 27 more genes
    nsv6637467copy number variation1nstd102humanPathogenic GRCh37 chr18: 53,624,405-78,014,123 , GRCh38.p12 chr18: 55,957,174-80,256,240 RPL9P31, LOC100422317, 277 more genes
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