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Items: 1 to 20 of 155

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5896722copy number variation1nstd209human GRCh38 chr2: 203,728,538-203,729,552 , GRCh37.p13 chr2: 204,593,261-204,594,275 CD28
    nsv5690635mobile element insertion1nstd211human GRCh38 chr2: 203,738,242-203,738,242 , GRCh37.p13 chr2: 204,602,965-204,602,965 CD28
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5398223mobile element insertion1nstd206human GRCh38 chr2: 203,738,242-203,738,293 , GRCh37.p13 chr2: 204,602,965-204,603,016 CD28
    nsv5077679mobile element insertion1nstd203human GRCh38 chr2: 203,723,336-203,723,336 , GRCh37.p13 chr2: 204,588,059-204,588,059 CD28
    nsv5077442mobile element insertion1nstd203human GRCh38 chr2: 203,723,332-203,723,337 , GRCh37.p13 chr2: 204,588,055-204,588,060 CD28
    nsv4913848copy number variation1nstd200human GRCh38 chr2: 203,739,051-203,749,909 , GRCh37.p13 chr2: 204,603,774-204,614,632 CD28
    nsv4913844copy number variation1nstd200human GRCh38 chr2: 203,378,193-203,769,525 , GRCh37.p13 chr2: 204,242,916-204,634,248 CD28, ABI2, 4 more genes
    nsv4804557copy number variation1nstd200human GRCh37 chr2: 204,242,916-204,634,248 , GRCh38.p12 chr2: 203,378,193-203,769,525 LOC729532, LOC100287498, 4 more genes
    nsv4795611copy number variation1nstd200human GRCh37 chr2: 204,593,263-204,594,276 , GRCh38.p12 chr2: 203,728,540-203,729,553 CD28
    nsv4769348copy number variation1nstd102humanUncertain significance GRCh37 chr2: 204,312,776-208,235,204 , GRCh38.p12 chr2: 203,448,053-207,370,480 PARD3B, DSTNP5, 50 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
    nsv4728545copy number variation1nstd102humanPathogenic GRCh37 chr2: 204,445,619-212,580,788 , GRCh38.p12 chr2: 203,580,896-211,716,063 FASTKD2, MYL6BP1, 110 more genes
    nsv4681433copy number variation1nstd102humanPathogenic GRCh37 chr2: 204,309,591-204,822,606 , GRCh38.p12 chr2: 203,444,868-203,957,883 RAPH1, CD28, 8 more genes
    nsv4674597copy number variation1nstd102humanPathogenic GRCh37 chr2: 201,106,432-204,901,548 , GRCh38.p12 chr2: 200,241,709-204,036,825 KIAA2012-AS1, SNORD11, 113 more genes
    nsv4674491copy number variation1nstd102humanPathogenic GRCh37 chr2: 202,772,963-205,218,660 , GRCh38.p12 chr2: 201,908,240-204,353,937 LOC100287425, WDR12, 55 more genes
    nsv4674383copy number variation1nstd102humanPathogenic GRCh37 chr2: 163,233,162-211,927,188 , GRCh38.p12 chr2: 162,376,652-211,062,464 SNORA41, LOC101929633, 663 more genes
    nsv4595277copy number variation1nstd183human GRCh37 chr2: 203,773,467-206,480,054 , GRCh38.p12 chr2: 202,908,744-205,615,330 MRPL50P2, RNU6-474P, 27 more genes
    nsv4436532copy number variation1nstd102humanPathogenic GRCh37 chr2: 188,926,928-225,298,653 , GRCh38.p12 chr2: 188,062,201-224,433,936 MARS2, KRT18P19, 575 more genes
    nsv4316119inversion1nstd166human GRCh37.p13 chr2: 187,130,612-218,396,189 , GRCh38.p12 chr2: 186,265,885-217,531,466 , ACADL, 453 more genes
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