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Items: 1 to 20 of 437

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5965910insertion1nstd209human GRCh38 chr4: 88,577,605-88,577,605 , GRCh37.p13 chr4: 89,498,756-89,498,756 HERC3
    nsv5963717insertion1nstd209human GRCh38 chr4: 88,545,430-88,545,430 , GRCh37.p13 chr4: 89,466,581-89,466,581 HERC3
    nsv5949136insertion1nstd209human GRCh38 chr4: 88,699,313-88,699,313 , GRCh37.p13 chr4: 89,620,464-89,620,464 HERC3
    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
    nsv5893328copy number variation1nstd209human GRCh38 chr4: 88,601,757-88,602,071 , GRCh37.p13 chr4: 89,522,908-89,523,222 HERC3
    nsv5891156copy number variation1nstd209human GRCh38 chr4: 88,573,718-88,573,991 , GRCh37.p13 chr4: 89,494,869-89,495,142 HERC3
    nsv5840168copy number variation1nstd209human GRCh38 chr4: 88,572,599-88,574,998 , GRCh37.p13 chr4: 89,493,750-89,496,149 HERC3
    nsv5840167copy number variation1nstd209human GRCh38 chr4: 88,548,277-88,585,952 , GRCh37.p13 chr4: 89,469,428-89,507,103 RN7SKP244, HERC3
    nsv5692959mobile element insertion1nstd211human GRCh38 chr4: 88,524,516-88,524,516 , GRCh37.p13 chr4: 89,445,667-89,445,667 PIGY-DT, HERC3
    nsv5675942mobile element insertion1nstd211human GRCh38 chr4: 88,643,643-88,643,643 , GRCh37.p13 chr4: 89,564,794-89,564,794 HERC3
    nsv5675453mobile element insertion1nstd211human GRCh38 chr4: 88,609,531-88,609,531 , GRCh37.p13 chr4: 89,530,682-89,530,682 HERC3
    nsv5623383insertion1nstd207human GRCh38 chr4: 88,577,605-88,577,605 , GRCh37.p13 chr4: 89,498,756-89,498,756 HERC3
    nsv5616626insertion1nstd207human GRCh38 chr4: 88,699,308-88,699,308 , GRCh37.p13 chr4: 89,620,459-89,620,459 HERC3
    nsv5615416insertion2nstd207human GRCh38 chr4: 88,698,989-88,698,989 , GRCh37.p13 chr4: 89,620,140-89,620,140 HERC3
    nsv5614767insertion1nstd207human GRCh38 chr4: 88,577,616-88,577,616 , GRCh37.p13 chr4: 89,498,767-89,498,767 HERC3
    nsv5611069insertion2nstd207human GRCh38 chr4: 88,699,285-88,699,285 , GRCh37.p13 chr4: 89,620,436-89,620,436 HERC3
    nsv5570536copy number variation1nstd207human GRCh38 chr4: 88,601,757-88,602,071 , GRCh37.p13 chr4: 89,522,908-89,523,222 HERC3
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5547030insertion1nstd206human GRCh38 chr4: 68,996,170-113,894,177 , GRCh37.p13 chr4: 69,861,888-114,815,333 , MIR548AH, 616 more genes
    nsv5469351copy number variation1nstd206human GRCh38 chr4: 88,539,274-88,539,369 , GRCh37.p13 chr4: 89,460,425-89,460,520 HERC3
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