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Items: 1 to 20 of 157

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5962716insertion1nstd209human GRCh38 chr2: 236,542,914-236,542,914 , GRCh37.p13 chr2: 237,451,557-237,451,557 ACKR3
    nsv5730703mobile element insertion1nstd211human GRCh38 chr2: 236,547,266-236,547,266 , GRCh37.p13 chr2: 237,455,909-237,455,909 ACKR3
    nsv5673218copy number variation1nstd102humanPathogenic GRCh37 chr2: 237,481,970-238,305,470 , GRCh38.p12 chr2: 236,573,327-237,396,827 LOC105373946, LOC105373949, 13 more genes
    nsv5619708insertion1nstd207human GRCh38 chr2: 236,542,914-236,542,914 , GRCh37.p13 chr2: 237,451,557-237,451,557 ACKR3
    nsv5557270mobile element insertion1nstd206human GRCh38 chr2: 236,547,266-236,547,317 , GRCh37.p13 chr2: 237,455,909-237,455,960 ACKR3
    nsv5548656insertion1nstd206human GRCh38 chr2: 236,542,914-236,542,914 , GRCh37.p13 chr2: 237,451,557-237,451,557 ACKR3
    nsv5381323copy number variation1nstd102humanPathogenic GRCh37 chr2: 237,201,756-243,048,760 , GRCh38.p12 chr2: 236,293,113-242,106,609 LRRFIP1, GPR35, 133 more genes
    nsv5366896translocation1nstd200human GRCh38 chr2: 236,570,913-236,570,913 , GRCh38 chr2: 236,571,285-236,571,285 , GRCh37.p13 chr2: 237,479,556-237,479,556 , GRCh37.p13 chr2: 237,479,928-237,479,928 ACKR3
    nsv5366895translocation1nstd200human GRCh38 chr2: 236,570,655-236,570,655 , GRCh38 chr2: 236,571,292-236,571,292 , GRCh37.p13 chr2: 237,479,935-237,479,935 , GRCh37.p13 chr2: 237,479,298-237,479,298 ACKR3
    nsv5318856copy number variation1nstd204human GRCh38.p13 chr2: 236,094,899-237,206,460 , GRCh37.p13 chr2: 237,003,543-238,115,103 , LOC105373948, 20 more genes
    nsv5212471copy number variation1nstd204human GRCh38.p13 chr2: 236,557,632-236,580,623 , GRCh37.p13 chr2: 237,466,275-237,489,266 , ACKR3
    nsv5208976copy number variation1nstd204human GRCh38.p13 chr2: 236,358,901-237,206,400 , GRCh37.p13 chr2: 237,267,544-238,115,043 , LOC105373950, 14 more genes
    nsv4804707copy number variation1nstd200human GRCh37 chr2: 237,003,550-238,115,096 , GRCh38.p12 chr2: 236,094,906-237,206,453 , LOC105373949, 20 more genes
    nsv4790036copy number variation1nstd200human GRCh37 chr2: 237,473,202-237,473,286 , GRCh38.p12 chr2: 236,564,559-236,564,643 , ACKR3
    nsv4768328copy number variation1nstd102humanPathogenic GRCh37 chr2: 233,110,452-243,028,452 , GRCh38.p12 chr2: 232,245,742-242,086,301 LOC107985836, LOC105373980, 217 more genes
    nsv4753496insertion1nstd199human GRCh37 chr2: 237,451,553-237,451,553 , GRCh38.p12 chr2: 236,542,910-236,542,910 ACKR3
    nsv4728725copy number variation1nstd102humanPathogenic GRCh37 chr2: 178,397,959-243,007,457 , GRCh38.p12 chr2: 177,533,231-242,065,306 LOC105376755, FZD7, 1013 more genes
    nsv4724159insertion2nstd186human GRCh37 chr2: 237,451,557-237,451,557 , GRCh38.p12 chr2: 236,542,914-236,542,914 ACKR3
    nsv4685307insertion1nstd194human GRCh37 chr2: 237,451,557-237,451,557 , GRCh38.p12 chr2: 236,542,914-236,542,914 ACKR3
    nsv4683272copy number variation1nstd102humanUncertain significance GRCh37 chr2: 237,481,970-238,296,837 , GRCh38.p12 chr2: 236,573,327-237,388,194 COPS8-DT, RNU6-1051P, 13 more genes
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