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Items: 1 to 20 of 211

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7074645inversion1nstd229human GRCh38 chr18: 30,537,670-35,063,371 , GRCh37.p13 chr18: 28,117,636-32,643,335 DSC1, RN7SKP44, 46 more genes
    nsv7071971inversion1nstd229human GRCh38 chr18: 31,938,930-32,318,381 , GRCh37.p13 chr18: 29,518,893-29,898,344 TRAPPC8, RNA5SP453, 9 more genes
    nsv7004076copy number variation1nstd229human GRCh38 chr18: 31,888,813-32,220,544 , GRCh37.p13 chr18: 29,468,776-29,800,507 TRAPPC8, RNU6-1050P, 9 more genes
    nsv7003751copy number variation1nstd229human GRCh38 chr18: 32,126,701-32,318,400 , GRCh37.p13 chr18: 29,706,664-29,898,363 GAREM1, RNF138, 3 more genes
    nsv6624149copy number variation1nstd224human GRCh37 chr18: 29,731,080-29,806,853 , GRCh38.p12 chr18: 32,151,117-32,226,890 MEP1B, CLUHP6, 1 more genes
    nsv6586488inversion1nstd223human GRCh38 chr18: 31,938,930-32,318,379 , GRCh37.p13 chr18: 29,518,893-29,898,342 MEP1B, RNF138, 9 more genes
    nsv6586126inversion1nstd223human GRCh38 chr18: 31,785,259-32,556,165 , GRCh37.p13 chr18: 29,365,222-30,136,128 WBP11P1, LOC100421591, 13 more genes
    nsv6534515copy number variation1nstd223human GRCh38 chr18: 32,151,901-32,231,000 , GRCh37.p13 chr18: 29,731,864-29,810,963 MEP1B, CLUHP6, 1 more genes
    nsv6518564copy number variation1nstd223human GRCh38 chr18: 32,120,858-32,508,311 , GRCh37.p13 chr18: 29,700,821-30,088,274 MEP1B, RNF138, 4 more genes
    nsv6315530copy number variation1nstd102humanPathogenic GRCh37 chr18: 1-78,077,248 , GRCh38.p12 chr18: 10,001-80,259,271 LOC105372145, LOC105372016, 947 more genes
    nsv6314722copy number variation1nstd102humanPathogenic GRCh37 chr18: 1,262,334-53,254,751 , GRCh38.p12 chr18: 1,262,333-55,587,520 LOC107985176, ZNF521, 632 more genes
    nsv6291549copy number variation1nstd102humanLikely benign GRCh37 chr18: 29,734,579-29,807,636 , GRCh38.p12 chr18: 32,154,616-32,227,673 MEP1B, CLUHP6, 1 more genes
    nsv6133439copy number variation1nstd213human GRCh37 chr18: 28,680,000-49,600,001 , GRCh38.p12 chr18: 31,100,037-52,073,631 ATP5F1A, DSC1, 240 more genes
    nsv6133333copy number variation1nstd213human GRCh37 chr18: 27,400,000-52,060,001 , GRCh38.p12 chr18: 29,820,035-54,532,766 ATP5F1A, DCC, 259 more genes
    nsv6133332copy number variation1nstd213human GRCh37 chr18: 24,970,000-32,810,001 , GRCh38.p12 chr18: 27,390,036-35,230,037 DSC2, DTNA, 61 more genes
    nsv6112802copy number variation1nstd102humanPathogenic GRCh37 chr18: 23,626,739-78,014,976 , GRCh38.p12 chr18: 26,046,775-80,257,093 RPL9P31, LINC02582, 595 more genes
    nsv5321444copy number variation1nstd204human GRCh37.p13 chr18: 29,731,981-29,810,913 , GRCh38.p13 chr18: 32,152,018-32,230,950 MEP1B, CLUHP6, 1 more genes
    nsv5289333copy number variation1nstd204human GRCh38.p13 chr18: 32,152,401-32,230,900 , GRCh37.p13 chr18: 29,732,364-29,810,863 RNA5SP453, MEP1B, 1 more genes
    nsv5287981copy number variation1nstd204human GRCh38.p13 chr18: 32,190,075-32,197,224 , GRCh37.p13 chr18: 29,770,038-29,777,187 CLUHP6, MEP1B
    nsv5282232copy number variation1nstd204human GRCh38.p13 chr18: 32,193,301-32,231,000 , GRCh37.p13 chr18: 29,773,264-29,810,963 MEP1B, CLUHP6
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