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Items: 1 to 20 of 578

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5965567insertion1nstd209human GRCh38 chr2: 165,617,311-165,617,311 , GRCh37.p13 chr2: 166,473,821-166,473,821 CSRNP3
    nsv5954062insertion1nstd209human GRCh38 chr2: 165,666,934-165,666,934 , GRCh37.p13 chr2: 166,523,444-166,523,444 CSRNP3
    nsv5902959copy number variation1nstd209human GRCh38 chr2: 165,666,449-165,666,630 , GRCh37.p13 chr2: 166,522,959-166,523,140 CSRNP3
    nsv5901177copy number variation1nstd209human GRCh38 chr2: 165,652,172-165,652,845 , GRCh37.p13 chr2: 166,508,682-166,509,355 CSRNP3
    nsv5889026copy number variation1nstd209human GRCh38 chr2: 165,662,127-165,662,176 , GRCh37.p13 chr2: 166,518,637-166,518,686 CSRNP3
    nsv5888779copy number variation1nstd209human GRCh38 chr2: 165,625,863-165,626,154 , GRCh37.p13 chr2: 166,482,373-166,482,664 CSRNP3
    nsv5831417copy number variation1nstd209human GRCh38 chr2: 165,629,844-165,632,115 , GRCh37.p13 chr2: 166,486,354-166,488,625 CSRNP3
    nsv5682822mobile element insertion2nstd211human GRCh38 chr2: 165,544,526-165,544,526 , GRCh37.p13 chr2: 166,401,036-166,401,036 CSRNP3
    nsv5675098mobile element insertion1nstd211human GRCh38 chr2: 165,562,126-165,562,126 , GRCh37.p13 chr2: 166,418,636-166,418,636 CSRNP3
    nsv5623096insertion1nstd207human GRCh38 chr2: 165,477,483-165,477,483 , GRCh37.p13 chr2: 166,333,993-166,333,993 CSRNP3
    nsv5613694insertion1nstd207human GRCh38 chr2: 165,544,512-165,544,512 , GRCh37.p13 chr2: 166,401,022-166,401,022 CSRNP3
    nsv5611894insertion1nstd207human GRCh38 chr2: 165,590,959-165,590,959 , GRCh37.p13 chr2: 166,447,469-166,447,469 CSRNP3
    nsv5610706insertion1nstd207human GRCh38 chr2: 165,482,057-165,482,057 , GRCh37.p13 chr2: 166,338,567-166,338,567 CSRNP3
    nsv5565899copy number variation1nstd207human GRCh38 chr2: 165,625,863-165,626,154 , GRCh37.p13 chr2: 166,482,373-166,482,664 CSRNP3
    nsv5564252copy number variation5nstd102humanPathogenic GRCh37 chr2: 165,946,660-167,168,266 , GRCh38.p12 chr2: 165,090,150-166,311,756 TTC21B-AS1, RN7SKP152, 11 more genes
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5543689insertion1nstd206human GRCh38 chr2: 165,617,326-165,617,362 , GRCh37.p13 chr2: 166,473,836-166,473,872 CSRNP3
    nsv5450622copy number variation1nstd206human GRCh38 chr2: 165,484,829-165,485,102 , GRCh37.p13 chr2: 166,341,339-166,341,612 CSRNP3
    nsv5449889copy number variation1nstd206human GRCh38 chr2: 165,658,195-165,658,257 , GRCh37.p13 chr2: 166,514,705-166,514,767 CSRNP3
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