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Items: 1 to 20 of 188

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5906411copy number variation1nstd209human GRCh38 chr2: 237,094,514-237,094,587 , GRCh37.p13 chr2: 238,003,157-238,003,230 COPS8
    nsv5678372mobile element insertion2nstd211human GRCh38 chr2: 237,085,636-237,085,636 , GRCh37.p13 chr2: 237,994,279-237,994,279 COPS8
    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
    nsv5606880insertion1nstd207human GRCh38 chr2: 237,088,360-237,088,360 , GRCh37.p13 chr2: 237,997,003-237,997,003 COPS8
    nsv5406882mobile element insertion1nstd206human GRCh38 chr2: 237,085,636-237,085,687 , GRCh37.p13 chr2: 237,994,279-237,994,330 COPS8
    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
    nsv5351242translocation1nstd200human GRCh38 chr2: 237,094,514-237,094,514 , GRCh38 chr2: 237,094,588-237,094,588 , GRCh37.p13 chr2: 238,003,157-238,003,157 , GRCh37.p13 chr2: 238,003,231-238,003,231 COPS8
    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
    nsv5217541copy number variation1nstd204human GRCh38.p13 chr2: 237,085,647-237,101,528 , GRCh37.p13 chr2: 237,994,290-238,010,171 COPS8
    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
    nsv5068936mobile element insertion1nstd203human GRCh38 chr2: 237,085,618-237,085,636 , GRCh37.p13 chr2: 237,994,261-237,994,279 COPS8
    nsv4914095copy number variation1nstd200human GRCh38 chr2: 236,653,819-237,181,967 , GRCh37.p13 chr2: 237,562,462-238,090,610 , COPS8, 7 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
    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
    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
    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
    nsv4674624copy number variation1nstd102humanPathogenic GRCh37 chr2: 234,791,927-242,783,384 , GRCh38.p12 chr2: 233,883,281-241,841,232 LOC93463, DUSP28, 151 more genes
    nsv4674620copy number variation1nstd102humanPathogenic GRCh37 chr2: 237,265,271-242,783,384 , GRCh38.p12 chr2: 236,356,628-241,841,232 OR6B2, COPS8, 122 more genes
    nsv4674274copy number variation1nstd102humanPathogenic GRCh37 chr2: 234,090,049-239,494,702 , GRCh38.p12 chr2: 233,181,403-238,586,061 LOC105373933, CEP19P1, 105 more genes
    nsv4674036copy number variation1nstd102humanPathogenic GRCh37 chr2: 236,172,348-241,611,309 , GRCh38.p12 chr2: 235,263,704-240,671,892 ILKAP, MLPH, 95 more genes
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