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Items: 1 to 20 of 335

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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
    nsv7137214copy number variation1nstd102humanPathogenic GRCh37 chr18: 66,057,406-78,014,123 , GRCh38.p12 chr18: 68,390,169-80,256,240 LOC105372228, MIR548AV, 132 more genes
    nsv7099035copy number variation1nstd102humanPathogenic GRCh37 chr18: 66,434,850-78,075,000 , GRCh38.p12 chr18: 68,767,613-80,259,271 LOC107985151, CD226, 129 more genes
    nsv7077303inversion1nstd229human GRCh38 chr18: 69,163,300-69,900,667 , GRCh37.p13 chr18: 66,830,537-67,567,903 LOC105372179, LOC107985136, 5 more genes
    nsv7070240inversion1nstd229human GRCh38 chr18: 69,057,919-71,853,595 , GRCh37.p13 chr18: 66,725,156-69,520,831 GTSCR1, LOC105372188, 28 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
    nsv7068468inversion1nstd229human GRCh38 chr18: 69,402,182-71,004,393 , GRCh37.p13 chr18: 67,069,418-68,671,629 SOCS6, RTTN, 15 more genes
    nsv7067516inversion1nstd229human GRCh38 chr18: 68,954,423-69,930,317 , GRCh37.p13 chr18: 66,621,660-67,597,553 CD226, LOC100418959, 6 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
    nsv7060398inversion1nstd229human GRCh38 chr18: 68,944,123-69,928,240 , GRCh37.p13 chr18: 66,611,360-67,595,476 LOC100418959, LOC107985134, 6 more genes
    nsv7060202inversion1nstd229human GRCh38 chr18: 69,130,939-71,212,159 , GRCh37.p13 chr18: 66,798,176-68,879,395 LOC105372185, LINC01910, 20 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
    nsv6638045copy number variation1nstd102humanPathogenic GRCh37 chr18: 66,530,142-78,014,123 , GRCh38.p12 chr18: 68,862,905-80,256,240 LOC105372211, LOC105372188, 128 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
    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
    nsv6315531copy number variation1nstd102humanPathogenic GRCh37 chr18: 61,289,055-78,014,123 , GRCh38.p12 chr18: 63,621,821-80,256,240 RN7SL795P, ZNF407, 169 more genes
    nsv6315530copy number variation1nstd102humanPathogenic GRCh37 chr18: 1-78,077,248 , GRCh38.p12 chr18: 10,001-80,259,271 LOC105372145, LOC105372016, 947 more genes
    nsv6315301copy number variation1nstd102humanPathogenic GRCh38 chr18: 61,490,305-80,247,612 , GRCh37.p13 chr18: 59,157,538-78,005,495 RN7SL705P, LOC105372166, 196 more genes
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