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Items: 1 to 20 of 511

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7075760inversion1nstd229human GRCh38 chr19: 54,368,885-57,042,988 , GRCh37.p13 chr19: 55,595,687-57,554,356 ZSCAN5C, TMEM190, 137 more genes
    nsv7067331inversion1nstd229human GRCh38 chr19: 54,730,353-56,291,074 , GRCh37.p13 chr19: 55,595,687-56,802,443 NLRP2, KIR2DP1, 85 more genes
    nsv7063630inversion1nstd229human GRCh38 chr19: 54,312,295-55,433,689 , GRCh37.p13 chr19|NW_004166865.1: 286,662-1,058,686 BRSK1, VN1R104P, 69 more genes
    nsv7062087inversion1nstd229human GRCh38 chr19: 54,368,882-57,042,981 , GRCh37.p13 chr19: 55,595,687-57,554,349 BRSK1, ZIM2, 137 more genes
    nsv7016915copy number variation1nstd229human GRCh38 chr19: 54,865,130-54,865,232 , GRCh37.p13 chr19|NW_004166865.1: 839,498-839,600 KIR3DL2
    nsv7016121copy number variation1nstd229human GRCh38 chr19: 54,824,601-54,858,700 , GRCh37.p13 chr19|NW_004166865.1: 798,969-833,068 KIR2DS4, KIR3DL2, 1 more genes
    nsv7015941copy number variation1nstd229human GRCh38 chr19: 54,820,101-54,858,700 , GRCh37.p13 chr19|NW_004166865.1: 794,469-833,068 KIR3DL2, KIR2DS4, 1 more genes
    nsv7015177copy number variation1nstd229human GRCh38 chr19: 54,857,442-54,857,494 , GRCh37.p13 chr19|NW_004166865.1: 831,810-831,862 KIR3DL2
    nsv7014980copy number variation1nstd229human GRCh38 chr19: 54,852,601-54,869,400 , GRCh37.p13 chr19|NW_004166865.1: 826,969-843,768 RNU6-222P, KIR3DL2
    nsv7014849copy number variation1nstd229human GRCh38 chr19: 54,824,501-54,857,800 , GRCh37.p13 chr19|NW_004166865.1: 798,869-832,168 KIR2DS4, KIR3DL2, 1 more genes
    nsv7014788copy number variation1nstd229human GRCh38 chr19: 54,824,901-54,859,000 , GRCh37.p13 chr19|NW_004166865.1: 799,269-833,368 KIR3DL1, KIR3DL2, 1 more genes
    nsv7012300copy number variation1nstd229human GRCh38 chr19: 54,749,087-54,860,882 , GRCh37.p13 chr19|NW_004166865.1: 723,454-835,250 KIR2DS4, KIR3DL2, 7 more genes
    nsv7011666copy number variation1nstd229human GRCh38 chr19: 54,810,268-54,879,279 , GRCh37.p13 chr19|NW_004166865.1: 784,636-853,647 KIR2DS4, KIR3DL2, 4 more genes
    nsv7011326copy number variation1nstd229human GRCh38 chr19: 54,821,701-54,859,000 , GRCh37.p13 chr19|NW_004166865.1: 796,069-833,368 KIR3DL1, KIR2DS4, 1 more genes
    nsv7009130copy number variation1nstd229human GRCh38 chr19: 54,824,701-54,860,000 , GRCh37.p13 chr19|NW_004166865.1: 799,069-834,368 KIR3DL1, KIR3DL2, 1 more genes
    nsv7006844copy number variation1nstd229human GRCh38 chr19: 54,731,601-54,922,000 , GRCh37.p13 chr19|NW_004166865.1: 705,968-896,368 LOC101928804, KIR3DL3, 12 more genes
    nsv7005495copy number variation1nstd229human GRCh38 chr19: 54,850,801-54,867,500 , GRCh37.p13 chr19|NW_004166865.1: 825,169-841,868 RNU6-222P, KIR3DL2
    nsv7005357copy number variation1nstd229human GRCh38 chr19: 54,851,101-54,867,500 , GRCh37.p13 chr19|NW_004166865.1: 825,469-841,868 RNU6-222P, KIR3DL2
    nsv7004650copy number variation1nstd229human GRCh38 chr19: 54,852,578-54,867,528 , GRCh37.p13 chr19|NW_004166865.1: 826,946-841,896 RNU6-222P, KIR3DL2
    nsv7003016copy number variation1nstd229human GRCh38 chr19: 54,822,601-54,858,700 , GRCh37.p13 chr19|NW_004166865.1: 796,969-833,068 KIR3DL1, KIR3DL2, 1 more genes
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