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Items: 1 to 20 of 246

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7074210inversion1nstd229human GRCh38 chr18: 45,861,287-52,164,943 , GRCh37.p13 chr18: 43,441,252-49,691,313 LOC105372100, RNA5SP458, 103 more genes
    nsv7069854inversion1nstd229human GRCh38 chr18: 47,098,958-47,099,001 , GRCh37.p13 chr18: 44,625,329-44,625,372 LOC105372098, KATNAL2
    nsv7065765inversion1nstd229human GRCh38 chr18: 46,426,327-48,440,063 , GRCh37.p13 chr18: 44,006,290-45,966,434 ZBTB7C, MIR4527, 29 more genes
    nsv7062073inversion1nstd229human GRCh38 chr18: 42,140,183-50,368,023 , GRCh37.p13 chr18: 39,720,147-47,894,393 ACAA2, MIR4320, 105 more genes
    nsv7060607inversion1nstd229human GRCh38 chr18: 46,563,922-48,670,215 , GRCh37.p13 chr18: 44,143,885-46,196,586 SKOR2, ELOA3DP, 32 more genes
    nsv7016782copy number variation1nstd229human GRCh38 chr18: 47,084,555-47,089,853 , GRCh37.p13 chr18: 44,610,926-44,616,224 KATNAL2, LOC105372098
    nsv7014203copy number variation1nstd229human GRCh38 chr18: 47,101,267-47,101,434 , GRCh37.p13 chr18: 44,627,638-44,627,805 LOC105372098, KATNAL2
    nsv7006151copy number variation1nstd229human GRCh38 chr18: 47,075,270-47,091,938 , GRCh37.p13 chr18: 44,601,641-44,618,309 KATNAL2, LOC105372098
    nsv7005545copy number variation1nstd229human GRCh38 chr18: 47,078,467-47,096,057 , GRCh37.p13 chr18: 44,604,838-44,622,428 KATNAL2, LOC105372098
    nsv7003766copy number variation1nstd229human GRCh38 chr18: 47,039,656-47,076,306 , GRCh37.p13 chr18: 44,566,027-44,602,677 LOC105372098, KATNAL2
    nsv6998773copy number variation1nstd229human GRCh38 chr18: 44,716,377-50,773,277 , GRCh37.p13 chr18: 42,296,342-48,299,647 LOC105372101, MTCO2P2, 95 more genes
    nsv6998560copy number variation1nstd229human GRCh38 chr18: 46,921,465-47,196,235 , GRCh37.p13 chr18: 44,501,428-44,722,606 ELOA3CP, ELOA2, 8 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
    nsv6291497copy number variation1nstd102humanUncertain significance GRCh37 chr18: 44,552,943-44,605,249 , GRCh38.p12 chr18: 47,026,572-47,078,878 ELOA2, KATNAL2, 2 more genes
    nsv6133445copy number variation1nstd213human GRCh37 chr18: 44,060,000-45,480,001 , GRCh38.p12 chr18: 46,480,037-47,953,630 SMAD2, PIAS2, 24 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
    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
    nsv6103971insertion1nstd212human GRCh38 chr18: 47,089,501-47,089,501 , GRCh37.p13 chr18: 44,615,872-44,615,872 KATNAL2, LOC105372098
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