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Items: 1 to 20 of 1642

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6131552mobile element insertion1nstd186human GRCh37 chr12: 67,443,914-67,443,937 , GRCh38.p12 chr12: 67,050,134-67,050,157 GRIP1
    nsv6114250mobile element insertion1nstd186human GRCh37 chr12: 67,011,588-67,011,639 , GRCh38.p12 chr12: 66,617,808-66,617,859 GRIP1
    nsv6114194mobile element insertion1nstd186human GRCh37 chr12: 66,906,361-66,906,412 , GRCh38.p12 chr12: 66,512,581-66,512,632 GRIP1
    nsv6112755copy number variation1nstd102humanPathogenic GRCh37 chr12: 65,251,705-75,263,379 , GRCh38.p12 chr12: 64,857,925-74,869,599 LINC02421, TBC1D15, 144 more genes
    nsv5977800insertion1nstd209human GRCh38 chr12: 66,826,746-66,826,746 , GRCh37.p13 chr12: 67,220,526-67,220,526 GRIP1
    nsv5973737insertion1nstd209human GRCh38 chr12: 66,617,790-66,617,790 , GRCh37.p13 chr12: 67,011,570-67,011,570 GRIP1
    nsv5970566insertion1nstd209human GRCh38 chr12: 66,512,565-66,512,565 , GRCh37.p13 chr12: 66,906,345-66,906,345 GRIP1
    nsv5968912insertion1nstd209human GRCh38 chr12: 66,414,935-66,414,935 , GRCh37.p13 chr12: 66,808,715-66,808,715 GRIP1
    nsv5947480copy number variation1nstd209human GRCh38 chr12: 66,628,547-66,640,711 , GRCh37.p13 chr12: 67,022,327-67,034,491 GRIP1
    nsv5947034copy number variation1nstd209human GRCh38 chr12: 66,832,281-66,834,725 , GRCh37.p13 chr12: 67,226,061-67,228,505 GRIP1
    nsv5945282copy number variation1nstd209human GRCh38 chr12: 66,723,221-66,723,282 , GRCh37.p13 chr12: 67,117,001-67,117,062 GRIP1
    nsv5944060copy number variation1nstd209human GRCh38 chr12: 66,362,372-66,363,208 , GRCh37.p13 chr12: 66,756,152-66,756,988 LOC105369811, GRIP1
    nsv5942664copy number variation1nstd209human GRCh38 chr12: 66,412,233-66,414,658 , GRCh37.p13 chr12: 66,806,013-66,808,438 GRIP1
    nsv5941834copy number variation1nstd209human GRCh38 chr12: 67,055,351-67,055,441 , GRCh37.p13 chr12: 67,449,131-67,449,221 GRIP1
    nsv5939040copy number variation1nstd209human GRCh38 chr12: 66,690,736-66,691,599 , GRCh37.p13 chr12: 67,084,516-67,085,379 GRIP1
    nsv5938082copy number variation1nstd209human GRCh38 chr12: 66,726,230-66,726,353 , GRCh37.p13 chr12: 67,120,010-67,120,133 GRIP1
    nsv5935390copy number variation1nstd209human GRCh38 chr12: 66,481,816-66,509,565 , GRCh37.p13 chr12: 66,875,596-66,903,345 GRIP1
    nsv5934052copy number variation1nstd209human GRCh38 chr12: 66,398,194-66,400,349 , GRCh37.p13 chr12: 66,791,974-66,794,129 GRIP1
    nsv5933425copy number variation1nstd209human GRCh38 chr12: 66,437,698-66,438,000 , GRCh37.p13 chr12: 66,831,478-66,831,780 GRIP1
    nsv5932826copy number variation1nstd209human GRCh38 chr12: 66,424,548-66,424,679 , GRCh37.p13 chr12: 66,818,328-66,818,459 GRIP1
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