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Items: 1 to 20 of 143

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974799inversion1nstd209human GRCh38 chr19: 12,342,936-19,691,231 , GRCh37.p13 chr19: 12,453,750-19,802,040 , GET3, 322 more genes
    nsv5932340copy number variation1nstd209human GRCh38 chr19: 16,160,057-16,164,081 , GRCh37.p13 chr19: 16,270,868-16,274,892 CIB3
    nsv5885517copy number variation1nstd209human GRCh38 chr19: 16,160,131-16,164,030 , GRCh37.p13 chr19: 16,270,942-16,274,841 CIB3
    nsv5532593copy number variation1nstd206human GRCh38 chr19: 16,149,437-16,169,997 , GRCh37.p13 chr19: 16,260,247-16,280,808 HSH2D, CIB3
    nsv5515415copy number variation1nstd206human GRCh38 chr19: 16,170,753-16,177,257 , GRCh37.p13 chr19: 16,281,564-16,288,068 CIB3
    nsv5041043inversion1nstd200human GRCh38 chr19: 11,963,569-20,150,886 , GRCh37.p13 chr19: 12,074,384-20,193,556 , USE1, 369 more genes
    nsv5014594copy number variation1nstd200human GRCh38 chr19: 16,169,078-16,172,340 , GRCh37.p13 chr19: 16,279,889-16,283,151 CIB3
    nsv5014593copy number variation1nstd200human GRCh38 chr19: 16,166,850-16,170,717 , GRCh37.p13 chr19: 16,277,661-16,281,528 CIB3
    nsv5012073copy number variation1nstd200human GRCh38 chr19: 16,167,918-16,175,501 , GRCh37.p13 chr19: 16,278,729-16,286,312 CIB3
    nsv5012072copy number variation1nstd200human GRCh38 chr19: 16,166,267-16,167,156 , GRCh37.p13 chr19: 16,277,078-16,277,967 CIB3
    nsv5012071copy number variation1nstd200human GRCh38 chr19: 16,160,096-16,164,083 , GRCh37.p13 chr19: 16,270,907-16,274,894 CIB3
    nsv5012070copy number variation1nstd200human GRCh38 chr19: 16,159,631-16,170,694 , GRCh37.p13 chr19: 16,270,442-16,281,505 CIB3
    nsv4864965copy number variation1nstd200human GRCh37 chr19: 16,277,661-16,281,528 , GRCh38.p12 chr19: 16,166,850-16,170,717 CIB3
    nsv4860502copy number variation1nstd200human GRCh37 chr19: 16,278,728-16,286,313 , GRCh38.p12 chr19: 16,167,917-16,175,502 CIB3
    nsv4860501copy number variation1nstd200human GRCh37 chr19: 16,270,907-16,274,894 , GRCh38.p12 chr19: 16,160,096-16,164,083 CIB3
    nsv4860500copy number variation1nstd200human GRCh37 chr19: 16,270,442-16,281,505 , GRCh38.p12 chr19: 16,159,631-16,170,694 CIB3
    nsv4729750copy number variation1nstd102humanPathogenic GRCh37 chr19: 14,286,624-20,956,753 , GRCh38.p12 chr19: 14,175,812-20,773,947 LOC105372309, RAB8A, 269 more genes
    nsv4632165copy number variation1nstd183human GRCh37 chr19: 16,164,883-16,303,015 , GRCh38.p12 chr19: 16,054,073-16,192,204 RAB8A, TPM4, 4 more genes
    nsv4457713copy number variation1nstd102humanUncertain significance GRCh37 chr19: 15,623,742-16,301,544 , GRCh38.p12 chr19: 15,512,931-16,190,733 CIB3, UCA1-AS1, 34 more genes
    nsv4268690copy number variation1nstd166human GRCh37.p13 chr19: 16,273,070-16,273,474 , GRCh38.p12 chr19: 16,162,259-16,162,663 CIB3
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