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Items: 1 to 20 of 477

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148161copy number variation1nstd102humanPathogenic GRCh38 chr4: 1-49,062,177 , GRCh37.p13 chr4: 507,005-49,064,194 SLIRPP2, STIM2-AS1, 659 more genes
    nsv7148157copy number variation1nstd102humanPathogenic GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396 OR7E84P, FAM193A, 764 more genes
    nsv7137196copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-34,512,694 , GRCh38.p12 chr4: 68,453-34,511,072 ECM1P2, LOC105378240, 482 more genes
    nsv7093424delins1nstd102humanUncertain significance GRCh38 chr4: 2,829,567-2,829,616 , GRCh37 chr4: 2,831,294-2,831,343 SH3BP2
    nsv7058018inversion1nstd229human GRCh38 chr4: 2,820,714-2,825,038 , GRCh37.p13 chr4: 2,822,441-2,826,765 SH3BP2
    nsv7056542inversion1nstd229human GRCh38 chr4: 2,810,870-2,830,283 , GRCh37.p13 chr4: 2,812,597-2,832,010 SH3BP2
    nsv7049289inversion1nstd229human GRCh38 chr4: 1,879,237-2,966,412 , GRCh37.p13 chr4: 1,880,964-2,968,139 RNF4, SCARNA22, 28 more genes
    nsv7043381inversion1nstd229human GRCh38 chr4: 2,806,632-2,824,415 , GRCh37.p13 chr4: 2,808,359-2,826,142 SH3BP2
    nsv7040457inversion1nstd229human GRCh38 chr4: 2,747,436-3,221,045 , GRCh37.p13 chr4: 2,749,163-3,222,772 HTT, NOP14-AS1, 10 more genes
    nsv7039441inversion1nstd229human GRCh38 chr4: 1,689,472-2,959,448 , GRCh37.p13 chr4: 1,691,199-2,961,175 NOP14-AS1, LOC112268460, 34 more genes
    nsv7038837inversion1nstd229human GRCh38 chr4: 2,818,183-2,820,887 , GRCh37.p13 chr4: 2,819,910-2,822,614 SH3BP2
    nsv6737374copy number variation1nstd229human GRCh38 chr4: 2,811,125-2,814,547 , GRCh37.p13 chr4: 2,812,852-2,816,274 SH3BP2
    nsv6734506copy number variation1nstd229human GRCh38 chr4: 2,800,703-2,806,512 , GRCh37.p13 chr4: 2,802,430-2,808,239 SH3BP2
    nsv6733497copy number variation1nstd229human GRCh38 chr4: 2,773,398-2,805,078 , GRCh37.p13 chr4: 2,775,125-2,806,805 SH3BP2, LOC102723763
    nsv6727851copy number variation1nstd229human GRCh38 chr4: 2,800,984-2,801,060 , GRCh37.p13 chr4: 2,802,711-2,802,787 SH3BP2
    nsv6727655copy number variation1nstd229human GRCh38 chr4: 2,802,616-2,802,669 , GRCh37.p13 chr4: 2,804,343-2,804,396 SH3BP2
    nsv6727233copy number variation1nstd229human GRCh38 chr4: 2,794,414-2,794,439 , GRCh37.p13 chr4: 2,796,141-2,796,166 SH3BP2
    nsv6727212copy number variation1nstd229human GRCh38 chr4: 2,817,091-2,821,990 , GRCh37.p13 chr4: 2,818,818-2,823,717 SH3BP2
    nsv6722077copy number variation1nstd229human GRCh38 chr4: 2,813,258-2,821,937 , GRCh37.p13 chr4: 2,814,985-2,823,664 SH3BP2
    nsv6721956copy number variation1nstd229human GRCh38 chr4: 2,838,060-2,843,187 , GRCh37.p13 chr4: 2,839,787-2,844,914 SH3BP2, ADD1
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