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Items: 1 to 20 of 140

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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
    nsv5650365insertion2nstd207human GRCh38 chr19: 13,764,287-13,764,287 , GRCh37.p13 chr19: 13,875,101-13,875,101 MRI1
    nsv5588503copy number variation1nstd207human GRCh38 chr19: 13,764,725-13,764,780 , GRCh37.p13 chr19: 13,875,539-13,875,594 MRI1
    nsv5530348copy number variation1nstd206human GRCh38 chr19: 13,769,650-13,770,366 , GRCh37.p13 chr19: 13,880,464-13,881,180 MRI1
    nsv5523710copy number variation1nstd206human GRCh38 chr19: 13,772,666-13,780,552 , GRCh37.p13 chr19: 13,883,480-13,891,366 MRI1, C19orf53
    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
    nsv5286173copy number variation1nstd204human GRCh38.p13 chr19: 13,764,801-14,012,000 , GRCh37.p13 chr19: 13,875,615-14,122,812 , MIR181C, 16 more genes
    nsv5282203copy number variation1nstd204human GRCh38.p13 chr19: 13,639,101-13,799,100 , GRCh37.p13 chr19: 13,749,915-13,909,914 YJU2B, ZSWIM4, 3 more genes
    nsv5175136mobile element insertion1nstd203human GRCh38 chr19: 13,767,861-13,767,885 , GRCh37.p13 chr19: 13,878,675-13,878,699 MRI1
    nsv5173279mobile element insertion1nstd203human GRCh38 chr19: 13,770,693-13,770,729 , GRCh37.p13 chr19: 13,881,507-13,881,543 MRI1
    nsv5041043inversion1nstd200human GRCh38 chr19: 11,963,569-20,150,886 , GRCh37.p13 chr19: 12,074,384-20,193,556 , USE1, 369 more genes
    nsv5011895copy number variation1nstd200human GRCh38 chr19: 13,772,832-13,774,815 , GRCh37.p13 chr19: 13,883,646-13,885,629 C19orf53, MRI1
    nsv4860393copy number variation1nstd200human GRCh37 chr19: 13,883,646-13,885,629 , GRCh38.p12 chr19: 13,772,832-13,774,815 MRI1, C19orf53
    nsv4755830insertion1nstd199human GRCh37 chr19: 13,875,132-13,875,132 , GRCh38.p12 chr19: 13,764,318-13,764,318 MRI1
    nsv3924466copy number variation1nstd102humanPathogenic NCBI36 chr19: 11,496,978-14,126,833 , GRCh38 chr19: 11,525,163-14,155,021 , GRCh37 chr19: 11,635,978-14,265,833 JUNB, ZNF442, 135 more genes
    nsv3923415copy number variation1nstd102humanPathogenic NCBI36 chr19: 10,286,934-14,020,806 , GRCh37 chr19: 10,425,934-14,159,806 , GRCh38 chr19: 10,315,258-14,048,994 MAN2B1, SWSAP1, 182 more genes
    nsv3922964copy number variation1nstd102humanPathogenic GRCh38 chr19: 10,319,474-13,777,860 , NCBI36 chr19: 10,291,150-13,749,674 , GRCh37 chr19: 10,430,150-13,888,674 SWSAP1, LOC105372284, 164 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
    nsv3913955copy number variation1nstd102humanUncertain significance GRCh37 chr19: 13,644,739-14,369,645 , GRCh38 chr19: 13,533,925-14,258,833 , NCBI36 chr19: 13,505,739-14,230,645 YJU2B, RN7SL619P, 30 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
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