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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094371copy number variation1nstd102humanPathogenic GRCh37 chr15: 42,686,444-42,697,047 , GRCh38.p12 chr15: 42,394,246-42,404,849 CAPN3
    nsv4681989copy number variation1nstd102humanPathogenic GRCh37 chr15: 42,688,988-42,697,047 , GRCh38.p12 chr15: 42,396,790-42,404,849 CAPN3
    nsv7094706copy number variation1nstd102humanPathogenic GRCh37 chr15: 42,694,952-42,698,151 , GRCh38.p12 chr15: 42,402,754-42,405,953 CAPN3
    nsv4451963copy number variation1nstd102humanPathogenic GRCh38 chr15: 42,359,796-42,360,124 , GRCh37 chr15: 42,651,994-42,652,322 CAPN3
    nsv4454674copy number variation1nstd102humanPathogenic GRCh38 chr15: 42,394,246-42,394,351 , GRCh37 chr15: 42,686,444-42,686,549 CAPN3
    nsv7093616insertion1nstd102humanPathogenic GRCh37 chr15: 42,701,546-42,701,546 , GRCh38 chr15: 42,409,348-42,409,348 CAPN3
    nsv4578639copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 42,684,837-42,686,539 , GRCh38.p12 chr15: 42,392,639-42,394,341 CAPN3
    nsv3884507copy number variation1nstd102humanLikely pathogenic GRCh38 chr15: 42,409,283-42,410,015 , GRCh37.p13 chr15: 42,701,481-42,702,213 CAPN3
    nsv5672739copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 42,695,919-42,695,985 , GRCh38.p12 chr15: 42,403,721-42,403,787 CAPN3
    nsv7094289copy number variation1nstd102humanPathogenic GRCh37 chr15: 42,651,994-42,695,985 , GRCh38.p12 chr15: 42,359,796-42,403,787 CAPN3, LOC105370794
    nsv4453398copy number variation1nstd102humanPathogenic GRCh38 chr15: 42,359,796-42,399,662 , GRCh37 chr15: 42,651,994-42,691,860 CAPN3, LOC105370794
    nsv6309726copy number variation1nstd102humanPathogenic GRCh37 chr15: 42,650,583-42,687,745 , GRCh38.p12 chr15: 42,358,385-42,395,547 CAPN3, LOC105370794
    nsv7148210copy number variation1nstd102humanPathogenic GRCh38 chr15: 42,349,336-42,378,932 , GRCh37.p13 chr15: 42,641,534-42,671,130 CAPN3, GANC
    nsv4450626copy number variation1nstd102humanPathogenic GRCh37 chr15: 42,682,131-42,703,991 , GRCh38 chr15: 42,389,933-42,411,793 CAPN3, ZNF106
    nsv7094705copy number variation1nstd102humanPathogenic GRCh37 chr15: 42,676,671-42,689,085 , GRCh38.p12 chr15: 42,384,473-42,396,887 CAPN3, LOC105370794
    nsv7094372copy number variation1nstd102humanPathogenic GRCh37 chr15: 42,691,680-42,703,981 , GRCh38.p12 chr15: 42,399,482-42,411,783 CAPN3, ZNF106
    nsv6309579copy number variation1nstd102humanPathogenic GRCh37 chr15: 42,676,661-42,686,559 , GRCh38.p12 chr15: 42,384,463-42,394,361 CAPN3, LOC105370794
    nsv4683627copy number variation1nstd102humanPathogenic GRCh37 chr15: 42,676,671-42,686,549 , GRCh38.p12 chr15: 42,384,473-42,394,351 CAPN3, LOC105370794
    nsv6309578copy number variation1nstd102humanPathogenic GRCh37 chr15: 42,676,661-42,684,940 , GRCh38.p12 chr15: 42,384,463-42,392,742 CAPN3, LOC105370794
    nsv4681325copy number variation1nstd102humanPathogenic GRCh37 chr15: 42,676,671-42,684,930 , GRCh38.p12 chr15: 42,384,473-42,392,732 CAPN3, LOC105370794
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