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Items: 1 to 20 of 1122

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5965281insertion1nstd209human GRCh38 chr4: 89,044,095-89,044,095 , GRCh37.p13 chr4: 89,965,246-89,965,246 FAM13A
    nsv5963049insertion1nstd209human GRCh38 chr4: 89,042,101-89,042,101 , GRCh37.p13 chr4: 89,963,252-89,963,252 FAM13A
    nsv5951485insertion1nstd209human GRCh38 chr4: 88,995,140-88,995,140 , GRCh37.p13 chr4: 89,916,291-89,916,291 FAM13A
    nsv5949105insertion1nstd209human GRCh38 chr4: 88,856,681-88,856,681 , GRCh37.p13 chr4: 89,777,832-89,777,832 FAM13A
    nsv5907258copy number variation1nstd209human GRCh38 chr4: 87,165,110-92,683,258 , GRCh37.p13 chr4: 88,086,262-93,604,409 HSP90AB3P, SPP1, 61 more genes
    nsv5903721copy number variation1nstd209human GRCh38 chr4: 88,893,479-88,893,673 , GRCh37.p13 chr4: 89,814,630-89,814,824 FAM13A
    nsv5898468copy number variation1nstd209human GRCh38 chr4: 88,760,309-88,760,630 , GRCh37.p13 chr4: 89,681,460-89,681,781 FAM13A
    nsv5895554copy number variation1nstd209human GRCh38 chr4: 88,912,214-88,912,265 , GRCh37.p13 chr4: 89,833,365-89,833,416 FAM13A
    nsv5894280copy number variation1nstd209human GRCh38 chr4: 88,852,240-88,852,563 , GRCh37.p13 chr4: 89,773,391-89,773,714 FAM13A
    nsv5891353copy number variation1nstd209human GRCh38 chr4: 89,096,880-89,097,269 , GRCh37.p13 chr4: 90,018,031-90,018,420 FAM13A
    nsv5887678copy number variation1nstd209human GRCh38 chr4: 88,913,107-88,913,390 , GRCh37.p13 chr4: 89,834,258-89,834,541 FAM13A
    nsv5840483copy number variation1nstd209human GRCh38 chr4: 88,955,419-89,012,746 , GRCh37.p13 chr4: 89,876,570-89,933,897 FAM13A, LOC105377327
    nsv5840430copy number variation1nstd209human GRCh38 chr4: 89,047,670-89,084,742 , GRCh37.p13 chr4: 89,968,821-90,005,893 FAM13A
    nsv5840170copy number variation1nstd209human GRCh38 chr4: 89,016,263-89,068,953 , GRCh37.p13 chr4: 89,937,414-89,990,104 FAM13A
    nsv5840169copy number variation1nstd209human GRCh38 chr4: 88,980,974-89,012,996 , GRCh37.p13 chr4: 89,902,125-89,934,147 FAM13A
    nsv5730573mobile element insertion1nstd211human GRCh38 chr4: 89,096,750-89,096,750 , GRCh37.p13 chr4: 90,017,901-90,017,901 FAM13A
    nsv5726869mobile element insertion1nstd211human GRCh38 chr4: 88,774,052-88,774,052 , GRCh37.p13 chr4: 89,695,203-89,695,203 FAM13A
    nsv5721989mobile element insertion2nstd211human GRCh38 chr4: 88,806,391-88,806,391 , GRCh37.p13 chr4: 89,727,542-89,727,542 FAM13A
    nsv5714861mobile element insertion2nstd211human GRCh38 chr4: 89,052,278-89,052,278 , GRCh37.p13 chr4: 89,973,429-89,973,429 FAM13A
    nsv5690352mobile element insertion2nstd211human GRCh38 chr4: 88,837,431-88,837,431 , GRCh37.p13 chr4: 89,758,582-89,758,582 FAM13A
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