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Items: 1 to 20 of 434

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7073609inversion1nstd229human GRCh38 chr18: 63,413,869-65,236,100 , GRCh37.p13 chr18: 61,081,102-62,903,336 SERPINB8, SERPINB5, 22 more genes
    nsv7072414inversion1nstd229human GRCh38 chr18: 59,526,812-66,942,199 , GRCh37.p13 chr18: 57,194,044-64,609,436 RPIAP1, LOC105372167, 77 more genes
    nsv7069827inversion1nstd229human GRCh38 chr18: 60,254,377-67,312,517 , GRCh37.p13 chr18: 57,921,610-64,979,754 RNU6-142P, TNFRSF11A, 63 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
    nsv7059846inversion1nstd229human GRCh38 chr18: 63,368,950-69,432,892 , GRCh37.p13 chr18: 61,036,183-67,100,128 SERPINB5, SERPINB8, 51 more genes
    nsv7017022copy number variation1nstd229human GRCh38 chr18: 64,085,714-64,133,743 , GRCh37.p13 chr18: 61,752,948-61,800,977 LINC01924, LINC00305
    nsv7014511copy number variation1nstd229human GRCh38 chr18: 64,104,406-64,108,746 , GRCh37.p13 chr18: 61,771,640-61,775,980 LINC00305, LINC01924
    nsv7009902copy number variation1nstd229human GRCh38 chr18: 64,123,920-64,142,353 , GRCh37.p13 chr18: 61,791,154-61,809,587 LINC01924, LINC00305
    nsv7009067copy number variation1nstd229human GRCh38 chr18: 64,137,162-64,137,645 , GRCh37.p13 chr18: 61,804,396-61,804,879 LINC00305, LINC01924
    nsv7006412copy number variation1nstd229human GRCh38 chr18: 63,817,401-66,637,500 , GRCh37.p13 chr18: 61,484,635-64,304,737 SERPINB8, LOC105372168, 18 more genes
    nsv7000376copy number variation1nstd229human GRCh38 chr18: 63,775,316-64,080,263 , GRCh37.p13 chr18: 61,442,550-61,747,497 SERPINB10, HMSD, 6 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
    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
    nsv6637200copy number variation1nstd102humanUncertain significance GRCh37 chr18: 61,483,089-64,304,841 , GRCh38.p12 chr18: 63,815,855-66,637,604 HMSD, SERPINB2, 18 more genes
    nsv6635689copy number variation1nstd227human GRCh37 chr18: 61,496,228-62,208,248 , GRCh38.p12 chr18: 63,828,994-64,541,013 SERPINB2, SERPINB8, 8 more genes
    nsv6585293inversion1nstd223human GRCh38 chr18: 63,817,377-68,462,605 , GRCh37.p13 chr18: 61,484,611-66,129,842 LOC105372169, LINC00305, 32 more genes
    nsv6577163inversion1nstd223human GRCh38 chr18: 64,089,156-64,089,846 , GRCh37.p13 chr18: 61,756,390-61,757,080 LINC00305
    nsv6535468copy number variation1nstd223human GRCh38 chr18: 64,121,801-64,123,400 , GRCh37.p13 chr18: 61,789,035-61,790,634 LINC01924, LINC00305
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