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Items: 1 to 20 of 89

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5532986copy number variation1nstd206human GRCh38 chr19: 8,695,984-8,696,314 , GRCh37.p13 chr19|NW_003871094.1: 125,954-126,284 , GRCh37.p13 chr19: 8,806,334-8,806,664 ACTL9
    nsv5526569copy number variation1nstd206human GRCh38 chr19: 8,345,242-8,989,493 , GRCh37.p13 chr19: 8,410,126-9,100,169 MIR4999, OR2Z1, 16 more genes
    nsv5359456translocation1nstd200human GRCh38 chr19: 8,695,984-8,695,984 , GRCh38 chr19: 8,696,314-8,696,314 , GRCh37.p13 chr19|NW_003871094.1: 125,954-125,954 , GRCh37.p13 chr19: 8,806,334-8,806,334 , GRCh37.p13 chr19|NW_003871094.1: 126,284-126,284 , GRCh37.p13 chr19: 8,806,664-8,806,664 ACTL9
    nsv5332210translocation1nstd200human GRCh37 chr19: 8,806,664-8,806,664 , GRCh37 chr19: 8,806,334-8,806,334 , GRCh38.p12 chr19: 8,695,984-8,695,984 , GRCh38.p12 chr19: 8,696,314-8,696,314 ACTL9
    nsv5297344copy number variation1nstd204human GRCh38.p13 chr19: 8,188,901-8,707,200 , GRCh37.p13 chr19: 8,253,785-8,634,914 RAB11B, HNRNPM, 17 more genes
    nsv5171694mobile element insertion1nstd203human GRCh38 chr19: 8,696,807-8,696,821 , GRCh37.p13 chr19|NW_003871094.1: 126,777-126,791 , GRCh37.p13 chr19: 8,807,157-8,807,171 ACTL9
    nsv5014477copy number variation1nstd200human GRCh38 chr19: 8,677,004-8,710,593 , GRCh37.p13 chr19: 8,786,839-8,820,946 , GRCh37.p13 chr19|NW_003871094.1: 106,974-140,563 NFILZ, ACTL9
    nsv5014467copy number variation1nstd200human GRCh37.p13 chr19|NW_003871094.1: 1-135,281 , GRCh38 chr19: 8,478,963-8,705,311 , GRCh37.p13 chr19: 8,634,912-8,815,660 PRAM1, ACTL9, 5 more genes
    nsv4864901copy number variation1nstd200human GRCh37 chr19: 8,786,839-8,820,946 , GRCh38.p12 chr19: 8,677,004-8,710,593 NFILZ, ACTL9
    nsv4864896copy number variation1nstd200human GRCh37 chr19: 8,543,847-8,815,660 , GRCh38.p12 chr19: 8,478,963-8,705,311 HNRNPM, ADAMTS10, 5 more genes
    nsv4729804copy number variation1nstd102humanUncertain significance GRCh37 chr19: 8,680,063-9,273,676 , GRCh38.p12 chr19: 8,615,177-9,163,000 OR7G1, OR7G2, 14 more genes
    nsv4729799copy number variation1nstd102humanUncertain significance GRCh37 chr19: 8,518,395-10,053,298 , GRCh38.p12 chr19: 8,453,511-9,942,622 ZNF426-DT, ADAMTS10, 61 more genes
    nsv4628826copy number variation1nstd183human GRCh37 chr19: 8,661,516-8,820,867 , GRCh38.p12 chr19: 8,596,632-8,710,514 ACTL9, NFILZ, 1 more genes
    nsv4536065copy number variation1nstd166human GRCh37.p13 chr19: 8,805,976-8,806,664 , GRCh38.p12 chr19: 8,695,626-8,696,314 ACTL9
    nsv4269019copy number variation1nstd166human GRCh37.p13 chr19: 8,799,185-9,251,695 , GRCh38.p12 chr19: 8,688,936-9,141,019 OR7G15P, OR7G1, 13 more genes
    nsv4263378copy number variation1nstd166human GRCh37.p13 chr19: 8,806,334-8,806,666 , GRCh38.p12 chr19: 8,695,984-8,696,316 ACTL9
    nsv4253019copy number variation1nstd166human GRCh37.p13 chr19: 8,788,500-8,830,100 , GRCh38.p12 chr19: 8,678,239-8,719,756 NFILZ, ACTL9
    nsv3970040copy number variation1nstd168human GRCh37.p13 chr19|NW_003871094.1: 6,822-128,895 , GRCh38 chr19: 8,576,852-8,698,925 , GRCh37.p13 chr19: 8,641,736-8,809,275 NFILZ, MYO1F, 2 more genes
    nsv3960012insertion1nstd168human GRCh38 chr19: 8,698,925-8,931,204 , GRCh37.p13 chr19: 8,809,275-8,926,179 , GRCh37.p13 chr19|NW_003871094.1: 128,895-245,473 MBD3L1, MUC16, 4 more genes
    nsv3914351copy number variation1nstd102humanPathogenic NCBI36 chr19: 1,923,244-9,620,555 , GRCh38 chr19: 1,972,245-9,648,879 , GRCh37 chr19: 1,972,244-9,759,555 SEMA6B, RANBP3-DT, 299 more genes
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