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Items: 1 to 20 of 574

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112816copy number variation1nstd102humanPathogenic GRCh37 chr16: 14,887,031-16,308,753 , GRCh38.p12 chr16: 14,793,174-16,214,896 , GRCh38.p12 chr16|NT_187607.1: 326,909-1,872,893 NTAN1, MIR3179-1, 50 more genes
    nsv6112786copy number variation1nstd102humanPathogenic GRCh37 chr16: 15,124,782-16,291,779 , GRCh38.p12 chr16: 15,030,925-16,197,922 , GRCh38.p12 chr16|NT_187607.1: 1,015,619-1,855,918 RNU6-213P, LOC105371102, 25 more genes
    nsv5967951inversion1nstd209human GRCh38 chr16: 13,469,401-22,726,308 , GRCh37.p13 chr16: 13,563,258-22,737,629 , ABCC6, 214 more genes
    nsv5942665copy number variation1nstd209human GRCh38 chr16: 15,376,746-15,376,817 , GRCh37.p13 chr16: 15,470,603-15,470,674 , NPIPA5
    nsv5928138copy number variation1nstd209human GRCh38 chr16: 15,180,124-18,091,718 , GRCh37.p13 chr16: 15,273,981-18,185,575 , LOC102723692, 42 more genes
    nsv5660770insertion1nstd207human GRCh38 chr16: 15,363,664-15,363,664 , GRCh37.p13 chr16: 15,457,521-15,457,521 , NPIPA5
    nsv5660613insertion1nstd207human GRCh38 chr16: 15,376,783-15,376,783 , GRCh37.p13 chr16: 15,470,640-15,470,640 , NPIPA5
    nsv5648357insertion1nstd207human GRCh38 chr16: 15,379,735-15,379,735 , GRCh37.p13 chr16: 15,473,592-15,473,592 , NPIPA5
    nsv5644600insertion1nstd207human GRCh38 chr16: 15,363,772-15,363,772 , GRCh37.p13 chr16: 15,457,629-15,457,629 , NPIPA5
    nsv5601235copy number variation1nstd207human GRCh38 chr16: 15,379,959-15,380,462 , GRCh37.p13 chr16: 15,473,816-15,474,319 , NPIPA5
    nsv5601024copy number variation1nstd207human GRCh38 chr16: 15,378,822-15,379,677 , GRCh37.p13 chr16: 15,472,679-15,473,534 , NPIPA5
    nsv5599532copy number variation1nstd207human GRCh38 chr16: 15,376,745-15,376,816 , GRCh37.p13 chr16: 15,470,602-15,470,673 , NPIPA5
    nsv5594732copy number variation1nstd207human GRCh38 chr16: 15,363,749-15,363,818 , GRCh37.p13 chr16: 15,457,606-15,457,675 , NPIPA5
    nsv5587728copy number variation1nstd207human GRCh38 chr16: 15,379,960-15,380,128 , GRCh37.p13 chr16: 15,473,817-15,473,985 , NPIPA5
    nsv5527878copy number variation1nstd206human GRCh38 chr16: 15,354,000-15,362,000 , GRCh37.p13 chr16: 15,447,857-15,455,857 , NPIPA5
    nsv5524792copy number variation1nstd206human GRCh38 chr16: 15,366,000-15,380,000 , GRCh37.p13 chr16: 15,459,857-15,473,857 , NPIPA5
    nsv5521901copy number variation1nstd206human GRCh38 chr16: 15,366,000-15,372,000 , GRCh37.p13 chr16: 15,459,857-15,465,857 , NPIPA5
    nsv5517977copy number variation1nstd206human GRCh38 chr16: 15,344,000-15,362,000 , GRCh37.p13 chr16: 15,437,857-15,455,857 , NPIPA5
    nsv5381790copy number variation1nstd102humanPathogenic GRCh37 chr16: 15,126,890-16,293,190 , GRCh38.p12 chr16: 15,033,033-16,199,333 , GRCh38.p12 chr16|NT_187607.1: 1,015,619-1,857,331 RRN3, CEP20, 25 more genes
    nsv5380983copy number variation1nstd102humanPathogenic GRCh37 chr16: 14,968,859-16,363,239 , GRCh38.p12 chr16: 14,875,002-16,269,382 , GRCh38.p12 chr16|NT_187607.1: 531,831-1,927,385 LOC102724984, LOC728138, 50 more genes
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