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Items: 1 to 20 of 256

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057662inversion1nstd229human GRCh38 chr6: 46,317,415-46,326,181 , GRCh37.p13 chr6: 46,285,152-46,293,918 LOC101926915, RCAN2
    nsv6794027copy number variation1nstd229human GRCh38 chr6: 46,282,383-46,282,441 , GRCh37.p13 chr6: 46,250,120-46,250,178 LOC101926915, RCAN2
    nsv6789661copy number variation1nstd229human GRCh38 chr6: 46,294,316-46,294,404 , GRCh37.p13 chr6: 46,262,053-46,262,141 LOC101926915, RCAN2
    nsv6787201copy number variation1nstd229human GRCh38 chr6: 46,283,915-46,286,695 , GRCh37.p13 chr6: 46,251,652-46,254,432 LOC101926915, RCAN2
    nsv6787011copy number variation1nstd229human GRCh38 chr6: 46,280,843-46,281,427 , GRCh37.p13 chr6: 46,248,580-46,249,164 LOC101926915, RCAN2
    nsv6783961copy number variation1nstd229human GRCh38 chr6: 46,315,454-46,322,365 , GRCh37.p13 chr6: 46,283,191-46,290,102 RCAN2, LOC101926915
    nsv6783642copy number variation1nstd229human GRCh38 chr6: 46,317,369-46,317,936 , GRCh37.p13 chr6: 46,285,106-46,285,673 LOC101926915, RCAN2
    nsv6783056copy number variation1nstd229human GRCh38 chr6: 46,296,359-46,423,008 , GRCh37.p13 chr6: 46,264,096-46,390,745 RCAN2, LOC101926915
    nsv6781705copy number variation1nstd229human GRCh38 chr6: 46,319,777-46,334,969 , GRCh37.p13 chr6: 46,287,514-46,302,706 RCAN2, LOC101926915
    nsv6778089copy number variation1nstd229human GRCh38 chr6: 46,300,530-46,306,749 , GRCh37.p13 chr6: 46,268,267-46,274,486 RCAN2, LOC101926915
    nsv6414063copy number variation1nstd223human GRCh38 chr6: 46,361,501-46,362,600 , GRCh37.p13 chr6: 46,329,238-46,330,337 RCAN2, LOC101926915
    nsv6410341copy number variation1nstd223human GRCh38 chr6: 46,280,201-46,280,900 , GRCh37.p13 chr6: 46,247,938-46,248,637 LOC101926915, RCAN2
    nsv6406949copy number variation1nstd223human GRCh38 chr6: 46,306,188-46,306,660 , GRCh37.p13 chr6: 46,273,925-46,274,397 RCAN2, LOC101926915
    nsv6402995copy number variation1nstd223human GRCh38 chr6: 46,319,777-46,334,968 , GRCh37.p13 chr6: 46,287,514-46,302,705 LOC101926915, RCAN2
    nsv6396660copy number variation1nstd223human GRCh38 chr6: 46,299,601-46,301,200 , GRCh37.p13 chr6: 46,267,338-46,268,937 LOC101926915, RCAN2
    nsv6314749copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 43,636,308-64,947,206 , GRCh38.p12 chr6: 43,668,571-64,237,313 ACTG1P9, CRISP1, 245 more genes
    nsv6282347insertion1nstd214human GRCh38 chr6: 46,282,383-46,282,383 , GRCh37.p13 chr6: 46,250,120-46,250,120 RCAN2, LOC101926915
    nsv6245100mobile element insertion1nstd215human GRCh38 chr6: 46,319,417-46,319,417 , GRCh37.p13 chr6: 46,287,154-46,287,154 RCAN2, LOC101926915
    nsv6135921copy number variation1nstd213human GRCh37 chr6: 34,700,000-52,650,001 , GRCh38.p12 chr6: 34,732,223-52,785,203 ACTG1P9, CRISP1, 361 more genes
    nsv6073407insertion1nstd212human GRCh38 chr6: 46,346,580-46,346,580 , GRCh37.p13 chr6: 46,314,317-46,314,317 LOC101926915, RCAN2
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