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Items: 1 to 20 of 105

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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
    nsv5884143copy number variation2nstd209human GRCh38 chr19: 14,584,580-14,589,613 , GRCh37.p13 chr19: 14,695,392-14,700,425 RN7SL842P, CLEC17A, 1 more genes
    nsv5598009copy number variation1nstd207human GRCh38 chr19: 14,583,366-14,587,619 , GRCh37.p13 chr19: 14,694,178-14,698,431 CLEC17A, RN7SL842P, 1 more genes
    nsv5518896copy number variation1nstd206human GRCh38 chr19: 14,584,000-14,589,500 , GRCh37.p13 chr19: 14,694,812-14,700,312 CLEC17A, RN7SL337P, 1 more genes
    nsv5300223copy number variation1nstd204human GRCh38.p13 chr19: 13,638,301-14,767,500 , GRCh37.p13 chr19: 13,749,115-14,878,312 , SNORA104, 53 more genes
    nsv5290575copy number variation1nstd204human GRCh38.p13 chr19: 14,584,480-14,587,741 , GRCh37.p13 chr19: 14,695,292-14,698,553 RN7SL842P, RN7SL337P, 1 more genes
    nsv5282493copy number variation1nstd204human GRCh38.p13 chr19: 14,399,601-14,623,200 , GRCh37.p13 chr19: 14,510,413-14,734,012 , DNAJB1, 15 more genes
    nsv5041043inversion1nstd200human GRCh38 chr19: 11,963,569-20,150,886 , GRCh37.p13 chr19: 12,074,384-20,193,556 , USE1, 369 more genes
    nsv5014572copy number variation1nstd200human GRCh38 chr19: 14,547,922-14,593,702 , GRCh37.p13 chr19: 14,658,734-14,704,514 , TECR, 4 more genes
    nsv5011960copy number variation1nstd200human GRCh38 chr19: 14,583,351-14,587,928 , GRCh37.p13 chr19: 14,694,163-14,698,740 RN7SL337P, CLEC17A, 1 more genes
    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
    nsv4676112copy number variation1nstd102humanPathogenic GRCh37 chr19: 14,368,330-15,712,368 , GRCh38.p12 chr19: 14,257,518-15,601,557 GIPC1, LOC100422106, 52 more genes
    nsv4632204copy number variation2nstd183human GRCh37 chr19: 14,695,453-14,704,392 , GRCh38.p12 chr19: 14,584,641-14,593,580 CLEC17A, RN7SL842P, 1 more genes
    nsv4426284copy number variation1nstd174human GRCh37 chr19: 14,695,453-14,704,392 , GRCh38.p12 chr19: 14,584,641-14,593,580 RN7SL337P, CLEC17A, 1 more genes
    nsv3963151insertion1nstd168human GRCh38 chr19: 14,529,813-14,600,316 , GRCh37.p13 chr19: 14,640,625-14,711,128 , DNAJB1, 7 more genes
    nsv3922457copy number variation1nstd102humanPathogenic GRCh37 chr19: 14,085,489-28,330,584 , GRCh38 chr19: 13,974,677-27,839,676 , NCBI36 chr19: 13,946,489-33,022,424 REX1BD, ZNF92P2, 416 more genes
    nsv3915094copy number variation1nstd102humanPathogenic GRCh38 chr19: 12,132,052-14,751,798 , NCBI36 chr19: 12,103,867-14,723,610 , GRCh37 chr19: 12,242,867-14,862,610 RN7SL619P, ZNF625-ZNF20, 123 more genes
    nsv3913730copy number variation1nstd102humanPathogenic NCBI36 chr19: 11,199,618-49,821,491 , GRCh37 chr19: 11,338,618-45,129,651 , GRCh38 chr19: 11,227,942-44,626,354 BCKDHA, ADGRE5, 1102 more genes
    nsv3912480copy number variation1nstd102humanPathogenic GRCh38 chr19: 12,580,427-14,742,673 , GRCh37 chr19: 12,691,241-14,853,485 , NCBI36 chr19: 12,552,241-14,714,485 GET3, ADGRE3, 100 more genes
    nsv3910918copy number variation1nstd102humanUncertain significance GRCh37 chr19: 14,588,573-15,244,464 , NCBI36 chr19: 14,449,573-15,105,464 , GRCh38 chr19: 14,477,761-15,133,653 GIPC1, TECR, 31 more genes
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