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Items: 1 to 20 of 213

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148210copy number variation1nstd102humanPathogenic GRCh38 chr15: 42,349,336-42,378,932 , GRCh37.p13 chr15: 42,641,534-42,671,130 CAPN3, GANC
    nsv7094706copy number variation1nstd102humanPathogenic GRCh37 chr15: 42,694,952-42,698,151 , GRCh38.p12 chr15: 42,402,754-42,405,953 CAPN3
    nsv7094705copy number variation1nstd102humanPathogenic GRCh37 chr15: 42,676,671-42,689,085 , GRCh38.p12 chr15: 42,384,473-42,396,887 LOC105370794, CAPN3
    nsv7094372copy number variation1nstd102humanPathogenic GRCh37 chr15: 42,691,680-42,703,981 , GRCh38.p12 chr15: 42,399,482-42,411,783 ZNF106, CAPN3
    nsv7094371copy number variation1nstd102humanPathogenic GRCh37 chr15: 42,686,444-42,697,047 , GRCh38.p12 chr15: 42,394,246-42,404,849 CAPN3
    nsv7094370copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 42,614,560-42,676,697 , GRCh38.p12 chr15: 42,322,362-42,384,499 CAPN3, GANC, 1 more genes
    nsv7094289copy number variation1nstd102humanPathogenic GRCh37 chr15: 42,651,994-42,695,985 , GRCh38.p12 chr15: 42,359,796-42,403,787 CAPN3, LOC105370794
    nsv7093616insertion1nstd102humanPathogenic GRCh37 chr15: 42,701,546-42,701,546 , GRCh38 chr15: 42,409,348-42,409,348 CAPN3
    nsv7062042inversion1nstd229human GRCh38 chr15: 38,786,391-46,534,887 , GRCh37.p13 chr15: 39,078,592-46,827,085 EHD4-AS1, PLA2G4B, 219 more genes
    nsv6973841copy number variation1nstd229human GRCh38 chr15: 41,876,434-43,470,213 , GRCh37.p13 chr15: 42,168,632-43,762,411 CAPN3, STARD9, 43 more genes
    nsv6971178copy number variation1nstd229human GRCh38 chr15: 42,314,001-42,371,300 , GRCh37.p13 chr15: 42,606,199-42,663,498 GANC, BNIP3P5, 1 more genes
    nsv6970347copy number variation1nstd229human GRCh38 chr15: 42,267,286-42,589,151 , GRCh37.p13 chr15: 42,559,484-42,881,349 LRRC57, GANC, 11 more genes
    nsv6968947copy number variation1nstd229human GRCh38 chr15: 42,396,863-42,531,333 , GRCh37.p13 chr15: 42,689,061-42,823,531 SNAP23, RNU6-188P, 3 more genes
    nsv6968879copy number variation1nstd229human GRCh38 chr15: 42,339,484-42,411,959 , GRCh37.p13 chr15: 42,631,682-42,704,157 ZNF106, CAPN3, 2 more genes
    nsv6968243copy number variation1nstd229human GRCh38 chr15: 42,370,518-42,375,196 , GRCh37.p13 chr15: 42,662,716-42,667,394 CAPN3
    nsv6962597copy number variation1nstd229human GRCh38 chr15: 42,364,582-42,395,597 , GRCh37.p13 chr15: 42,656,780-42,687,795 LOC105370794, CAPN3
    nsv6959406copy number variation1nstd229human GRCh38 chr15: 42,248,603-42,391,378 , GRCh37.p13 chr15: 42,540,801-42,683,576 LOC105370794, GANC, 3 more genes
    nsv6636133copy number variation1nstd102humanPathogenic GRCh37 chr15: 42,651,994-42,703,999 , GRCh38.p12 chr15: 42,359,796-42,411,801 ZNF106, LOC105370794, 1 more genes
    nsv6622892copy number variation1nstd224human GRCh37 chr15: 42,637,426-42,668,754 , GRCh38.p12 chr15: 42,345,228-42,376,556 CAPN3, GANC
    nsv6581724inversion1nstd223human GRCh38 chr15: 42,371,749-42,372,327 , GRCh37.p13 chr15: 42,663,947-42,664,525 CAPN3
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