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Items: 1 to 20 of 275

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5648627insertion1nstd207human GRCh38 chr15: 90,871,538-90,871,538 , GRCh37.p13 chr15: 91,414,768-91,414,768 FURIN
    nsv5527727copy number variation1nstd206human GRCh38 chr15: 90,875,107-90,875,216 , GRCh37.p13 chr15: 91,418,337-91,418,446 FURIN
    nsv5380768copy number variation1nstd102humanUncertain significance GRCh37 chr15: 91,290,623-91,512,067 , GRCh38.p12 chr15: 90,747,393-90,968,837 BLM, MAN2A2, 9 more genes
    nsv4769196insertion1nstd186human GRCh37 chr15: 91,414,769-91,414,769 , GRCh38.p12 chr15: 90,871,539-90,871,539 FURIN
    nsv4760515insertion1nstd199human GRCh37 chr15: 91,414,764-91,414,764 , GRCh38.p12 chr15: 90,871,534-90,871,534 FURIN
    nsv4729092copy number variation1nstd102humanPathogenic GRCh37 chr15: 86,962,053-102,531,392 , GRCh38.p12 chr15: 86,418,822-101,981,189 CHD2, MIR11181, 272 more genes
    nsv4685560insertion1nstd194human GRCh37 chr15: 91,414,769-91,414,769 , GRCh38.p12 chr15: 90,871,539-90,871,539 FURIN
    nsv4681314copy number variation1nstd102humanUncertain significance GRCh37 chr15: 91,326,042-91,512,067 , GRCh38.p12 chr15: 90,782,812-90,968,837 MAN2A2, UNC45A, 9 more genes
    nsv4675917copy number variation1nstd102humanUncertain significance GRCh37 chr15: 91,347,599-91,491,931 , GRCh38.p12 chr15: 90,804,369-90,948,701 FES, MAN2A2, 6 more genes
    nsv4675149copy number variation1nstd102humanPathogenic GRCh37 chr15: 87,189,245-102,429,112 , GRCh38.p12 chr15: 86,646,014-101,888,909 TTLL13, LINC00052, 264 more genes
    nsv4627887copy number variation1nstd183human GRCh37 chr15: 91,414,412-91,415,668 , GRCh38.p12 chr15: 90,871,182-90,872,438 FURIN
    nsv4457347copy number variation1nstd102humanUncertain significance GRCh37 chr15: 91,276,782-91,550,953 , GRCh38.p12 chr15: 90,733,551-91,007,723 BLM, MAN2A2, 10 more genes
    nsv4456778copy number variation1nstd102humanPathogenic GRCh37 chr15: 91,229,877-93,677,014 , GRCh38.p12 chr15: 90,686,646-93,133,785 H2AZ2P1, MAN2A2, 44 more genes
    nsv4456430copy number variation1nstd102humanPathogenic GRCh37 chr15: 90,288,175-102,429,112 , GRCh38.p12 chr15: 89,744,944-101,888,909 IQGAP1, LOC400464, 210 more genes
    nsv4414930copy number variation1nstd174human GRCh37 chr15: 91,414,234-91,415,668 , GRCh38.p12 chr15: 90,871,004-90,872,438 FURIN
    nsv4385824copy number variation1nstd173human GRCh37 chr15: 90,250,919-91,461,024 , GRCh38.p12 chr15: 89,707,688-90,917,794 , LOC100631255, 44 more genes
    nsv4377776copy number variation1nstd173human GRCh37 chr15: 86,980,083-93,499,239 , GRCh38.p12 chr15: 86,436,852-92,956,009 , RNU6-1111P, 136 more genes
    nsv4375224copy number variation1nstd173human GRCh37 chr15: 90,246,823-91,461,537 , GRCh38.p12 chr15: 89,703,592-90,918,307 , RNU6-1111P, 44 more genes
    nsv4350274copy number variation1nstd102humanPathogenic GRCh37 chr15: 83,883,823-92,165,844 , GRCh38.p12 chr15: 83,215,071-91,622,614 AKAP13, LOC105370972, 184 more genes
    nsv4250121copy number variation1nstd166human GRCh37.p13 chr15: 91,406,952-91,413,560 , GRCh38.p12 chr15: 90,863,722-90,870,330 FURIN
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