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Items: 1 to 20 of 165

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5609646insertion1nstd207human GRCh38 chr2: 235,504,439-235,504,439 , GRCh37.p13 chr2: 236,413,083-236,413,083 AGAP1-IT1, AGAP1
    nsv5317800copy number variation1nstd204human GRCh38.p13 chr2: 235,318,836-235,576,293 , GRCh37.p13 chr2: 236,227,480-236,484,937 AGAP1-IT1, AGAP1, 2 more genes
    nsv5218666copy number variation1nstd204human GRCh38.p13 chr2: 235,186,401-236,356,900 , GRCh37.p13 chr2: 236,095,045-237,265,543 , AGAP1, 15 more genes
    nsv5208703copy number variation1nstd204human GRCh38.p13 chr2: 235,497,021-235,522,451 , GRCh37.p13 chr2: 236,405,665-236,431,095 AGAP1, AGAP1-IT1, 1 more genes
    nsv4914076copy number variation1nstd200human GRCh38 chr2: 235,361,091-235,669,537 , GRCh37.p13 chr2: 236,269,735-236,578,181 LOC105373941, AGAP1, 2 more genes
    nsv4914071copy number variation1nstd200human GRCh38 chr2: 234,976,638-235,786,206 , GRCh37.p13 chr2: 235,885,282-236,694,850 , TNRC17, 9 more genes
    nsv4804697copy number variation1nstd200human GRCh37 chr2: 236,352,371-236,439,608 , GRCh38.p12 chr2: 235,443,727-235,530,964 AGAP1, AGAP1-IT1, 1 more genes
    nsv4804695copy number variation1nstd200human GRCh37 chr2: 236,227,490-236,484,935 , GRCh38.p12 chr2: 235,318,846-235,576,291 TNRC17, AGAP1, 2 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
    nsv4762193insertion1nstd199human GRCh37 chr2: 236,412,970-236,412,970 , GRCh38.p12 chr2: 235,504,326-235,504,326 AGAP1, AGAP1-IT1
    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
    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
    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
    nsv4673913copy number variation1nstd102humanPathogenic GRCh37 chr2: 230,814,690-242,783,384 , GRCh38.p12 chr2: 229,949,974-241,841,232 MIR2467, D2HGDH, 270 more genes
    nsv4585524copy number variation1nstd183human GRCh37 chr2: 235,994,328-236,432,130 , GRCh38.p12 chr2: 235,085,684-235,523,486 TNRC17, AGAP1, 4 more genes
    nsv4454839copy number variation1nstd102humanUncertain significance GRCh37 chr2: 236,201,133-236,510,465 , GRCh38.p12 chr2: 235,292,489-235,601,821 AGAP1-IT1, TNRC17, 2 more genes
    nsv4450331copy number variation1nstd102humanUncertain significance GRCh37 chr2: 235,992,185-236,431,911 , GRCh38.p12 chr2: 235,083,541-235,523,267 LOC105373940, AGAP1, 4 more genes
    nsv4435891copy number variation1nstd102humanPathogenic GRCh37 chr2: 210,779,657-239,879,183 , GRCh38.p12 chr2: 209,914,933-238,957,487 XRCC5, LINC01173, 494 more genes
    nsv4372512copy number variation1nstd173human GRCh37 chr2: 236,208,664-236,514,150 , GRCh38.p12 chr2: 235,300,020-235,605,506 LOC105373941, AGAP1, 2 more genes
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