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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5903892copy number variation1nstd209human GRCh38 chr2: 241,669,018-241,669,072 , GRCh37.p13 chr2: 242,608,433-242,608,487 ATG4B
    nsv5887649copy number variation1nstd209human GRCh38 chr2: 241,662,740-241,662,792 , GRCh37.p13 chr2: 242,602,155-242,602,207 ATG4B
    nsv5580777copy number variation1nstd207human GRCh38 chr2: 241,669,018-241,669,072 , GRCh37.p13 chr2: 242,608,433-242,608,487 ATG4B
    nsv5539910insertion1nstd206human GRCh38 chr2: 241,657,669-241,657,681 , GRCh37.p13 chr2: 242,597,084-242,597,096 ATG4B
    nsv5445351copy number variation1nstd206human GRCh38 chr2: 241,662,749-241,662,843 , GRCh37.p13 chr2: 242,602,164-242,602,258 ATG4B
    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
    nsv5218955mobile element deletion1nstd204human GRCh38.p13 chr2: 241,647,328-241,647,656 , GRCh37.p13 chr2: 242,586,743-242,587,071 ATG4B
    nsv5075776mobile element insertion1nstd203human GRCh38 chr2: 241,636,174-241,636,174 , GRCh37.p13 chr2: 242,575,589-242,575,589 ATG4B, THAP4
    nsv4914168copy number variation1nstd200human GRCh38 chr2: 241,590,801-241,964,363 , GRCh37.p13 chr2: 242,530,216-242,906,514 , ING5, 13 more genes
    nsv4914165copy number variation1nstd200human GRCh38 chr2: 241,510,828-241,897,945 , GRCh37.p13 chr2: 242,450,243-242,840,096 , LINC01237, 18 more genes
    nsv4871835mobile element deletion1nstd200human GRCh38 chr2: 241,647,337-241,647,648 , GRCh37.p13 chr2: 242,586,752-242,587,063 ATG4B
    nsv4787072mobile element deletion1nstd200human GRCh37 chr2: 242,586,752-242,587,063 , GRCh38.p12 chr2: 241,647,337-241,647,648 ATG4B
    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
    nsv4746059copy number variation1nstd199human GRCh37 chr2: 242,602,169-242,602,223 , GRCh38.p12 chr2: 241,662,754-241,662,808 ATG4B
    nsv4745696copy number variation1nstd199human GRCh37 chr2: 242,608,443-242,608,497 , GRCh38.p12 chr2: 241,669,028-241,669,082 ATG4B
    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
    nsv4728153copy number variation1nstd102humanUncertain significance GRCh37 chr2: 242,471,243-242,760,670 , GRCh38.p12 chr2: 241,531,828-241,819,342 ING5, D2HGDH, 10 more genes
    nsv4684239copy number variation1nstd102humanUncertain significance GRCh37 chr2: 238,863,455-243,048,760 , GRCh38.p12 chr2: 237,954,813-242,106,609 LOC285191, MTERF4, 103 more genes
    nsv4684149copy number variation1nstd102humanUncertain significance GRCh37 chr2: 241,791,028-242,842,568 , GRCh38.p12 chr2: 240,851,611-241,900,417 LOC105373978, ANO7, 39 more genes
    nsv4684141copy number variation1nstd102humanUncertain significance GRCh37 chr2: 241,810,850-243,048,760 , GRCh38.p12 chr2: 240,871,433-242,106,609 LOC105373974, LINC01238, 44 more genes
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