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Items: 1 to 20 of 370

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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
    nsv7069303inversion1nstd229human GRCh38 chr18: 66,516,237-71,816,578 , GRCh37.p13 chr18: 64,183,474-69,483,814 LOC100421257, LINC01899, 48 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
    nsv7061078inversion1nstd229human GRCh38 chr18: 68,840,470-69,158,584 , GRCh37.p13 chr18: 66,507,707-66,825,821 SDHCP1, CCDC102B, 3 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
    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
    nsv7017592copy number variation1nstd229human GRCh38 chr18: 68,980,907-69,107,187 , GRCh37.p13 chr18: 66,648,144-66,774,424 CCDC102B, LOC100418959
    nsv7017252copy number variation1nstd229human GRCh38 chr18: 68,937,126-69,081,612 , GRCh37.p13 chr18: 66,604,363-66,748,849 CCDC102B, LOC100418959
    nsv7011688copy number variation1nstd229human GRCh38 chr18: 68,848,595-69,158,583 , GRCh37.p13 chr18: 66,515,832-66,825,820 CCDC102B, SDHCP1, 3 more genes
    nsv7007972copy number variation1nstd229human GRCh38 chr18: 68,937,081-68,994,228 , GRCh37.p13 chr18: 66,604,318-66,661,465 CCDC102B, LOC100418959
    nsv7005789copy number variation1nstd229human GRCh38 chr18: 68,928,060-69,046,237 , GRCh37.p13 chr18: 66,595,297-66,713,474 LOC100418959, CCDC102B
    nsv7001174copy number variation1nstd229human GRCh38 chr18: 68,992,506-68,992,702 , GRCh37.p13 chr18: 66,659,743-66,659,939 CCDC102B, LOC100418959
    nsv7000925copy number variation1nstd229human GRCh38 chr18: 68,961,001-69,085,000 , GRCh37.p13 chr18: 66,628,238-66,752,237 CCDC102B, LOC100418959
    nsv6999207copy number variation1nstd229human GRCh38 chr18: 68,797,476-69,078,381 , GRCh37.p13 chr18: 66,464,713-66,745,618 CCDC102B, LOC100418959, 2 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
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