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Items: 1 to 20 of 175

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095478copy number variation1nstd102humanUncertain significance GRCh37 chr19: 33,167,170-36,643,309 , GRCh38.p12 chr19: 32,676,264-36,152,407 NFKBID, LRP3, 141 more genes
    nsv7070292inversion1nstd229human GRCh38 chr19: 36,142,842-36,168,669 , GRCh37.p13 chr19: 36,633,744-36,659,571 COX7A1, CAPNS1
    nsv7014713copy number variation1nstd229human GRCh38 chr19: 36,146,315-36,149,577 , GRCh37.p13 chr19: 36,637,217-36,640,479 CAPNS1, COX7A1
    nsv7011859copy number variation1nstd229human GRCh38 chr19: 36,129,095-36,144,329 , GRCh37.p13 chr19: 36,619,997-36,635,231 CAPNS1, LOC105372385
    nsv7011562copy number variation1nstd229human GRCh38 chr19: 36,143,128-36,145,805 , GRCh37.p13 chr19: 36,634,030-36,636,707 CAPNS1
    nsv7005713copy number variation1nstd229human GRCh38 chr19: 33,458,650-39,721,746 , GRCh37.p13 chr19: 33,949,556-40,212,386 , TYROBP, 259 more genes
    nsv7005456copy number variation1nstd229human GRCh38 chr19: 35,863,391-36,727,332 , GRCh37.p13 chr19: 36,354,293-37,218,234 ZNF146, CLIP3, 39 more genes
    nsv6999792copy number variation1nstd229human GRCh38 chr19: 36,044,743-36,166,690 , GRCh37.p13 chr19: 36,535,645-36,657,592 LOC105372385, COX7A1, 8 more genes
    nsv6624463copy number variation1nstd224human GRCh37 chr19: 36,636,905-36,728,088 , GRCh38.p12 chr19: 36,146,003-36,237,186 CAPNS1, ZNF565, 3 more genes
    nsv6534970copy number variation1nstd223human GRCh38 chr19: 36,126,631-36,143,766 , GRCh37.p13 chr19: 36,617,533-36,634,668 CAPNS1, LOC105372385
    nsv6527959copy number variation1nstd223human GRCh38 chr19: 36,138,059-36,138,496 , GRCh37.p13 chr19: 36,628,961-36,629,398 LOC105372385, CAPNS1
    nsv6518805copy number variation1nstd223human GRCh38 chr19: 36,129,094-36,144,328 , GRCh37.p13 chr19: 36,619,996-36,635,230 LOC105372385, CAPNS1
    nsv6517221copy number variation1nstd223human GRCh38 chr19: 36,147,580-36,148,528 , GRCh37.p13 chr19: 36,638,482-36,639,430 CAPNS1
    nsv6310629copy number variation1nstd102humanUncertain significance GRCh37 chr19: 35,521,725-36,643,309 , GRCh38.p12 chr19: 35,030,821-36,152,407 KRTDAP, WDR62, 78 more genes
    nsv6290300copy number variation1nstd102humanPathogenic GRCh37 chr19: 19,546,923-41,313,229 , GRCh38.p12 chr19: 19,436,114-40,807,324 ZNF420, LOC105372330, 574 more genes
    nsv6133701copy number variation1nstd213human GRCh37 chr19: 36,490,000-36,640,001 , GRCh38.p12 chr19: 35,999,098-36,149,099 CAPNS1, TBCB, 11 more genes
    nsv6133523copy number variation1nstd213human GRCh37 chr19: 34,000,000-42,200,001 , GRCh38.p12 chr19: 33,509,094-41,696,083 , ACTN4, 345 more genes
    nsv5935874copy number variation1nstd209human GRCh38 chr19: 36,129,530-36,153,993 , GRCh37.p13 chr19: 36,620,432-36,644,895 CAPNS1, COX7A1, 1 more genes
    nsv5935442copy number variation1nstd209human GRCh38 chr19: 36,140,368-36,144,022 , GRCh37.p13 chr19: 36,631,270-36,634,924 CAPNS1, LOC105372385
    nsv5874844copy number variation1nstd209human GRCh38 chr19: 36,140,329-36,144,073 , GRCh37.p13 chr19: 36,631,231-36,634,975 LOC105372385, CAPNS1
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