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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148056copy number variation1nstd102humanPathogenic GRCh37 chr2: 186,698,504-223,918,111 , GRCh38.p12 chr2: 185,833,777-223,053,393 DNAJB1P1, MTCO2P17, 580 more genes
    nsv7137033copy number variation1nstd102humanUncertain significance GRCh37 chr2: 219,204,506-219,222,815 , GRCh38.p12 chr2: 218,339,783-218,358,092 MIR6810, PNKD, 3 more genes
    nsv7096608copy number variation1nstd102humanUncertain significance GRCh37 chr2: 219,135,259-219,209,704 , GRCh38.p12 chr2: 218,270,536-218,344,981 LOC105373881, AAMP, 6 more genes
    nsv7096400copy number variation2nstd102humanUncertain significance GRCh37 chr2: 219,204,486-219,209,704 , GRCh38.p12 chr2: 218,339,763-218,344,981 PNKD, CATIP-AS2, 1 more genes
    nsv7048316inversion1nstd229human GRCh38 chr2: 217,690,925-222,070,373 , GRCh37.p13 chr2: 218,555,648-222,935,092 LOC105373895, CXCR2P1, 119 more genes
    nsv6697737copy number variation1nstd229human GRCh38 chr2: 218,278,917-218,284,815 , GRCh37.p13 chr2: 219,143,640-219,149,538 TMBIM1, MIR6513, 1 more genes
    nsv6697340copy number variation1nstd229human GRCh38 chr2: 218,271,805-218,271,903 , GRCh37.p13 chr2: 219,136,528-219,136,626 PNKD
    nsv6693999copy number variation1nstd229human GRCh38 chr2: 218,307,740-218,311,163 , GRCh37.p13 chr2: 219,172,463-219,175,886 PNKD, LOC105373881
    nsv6693617copy number variation1nstd229human GRCh38 chr2: 218,287,541-218,291,550 , GRCh37.p13 chr2: 219,152,264-219,156,273 TMBIM1, PNKD
    nsv6692655copy number variation1nstd229human GRCh38 chr2: 218,306,638-218,311,392 , GRCh37.p13 chr2: 219,171,361-219,176,115 LOC105373881, PNKD
    nsv6689222copy number variation1nstd229human GRCh38 chr2: 218,273,501-218,280,500 , GRCh37.p13 chr2: 219,138,224-219,145,223 TMBIM1, PNKD, 1 more genes
    nsv6685864copy number variation1nstd229human GRCh38 chr2: 216,932,763-218,687,760 , GRCh37.p13 chr2: 217,797,486-219,552,483 LOC105373872, IGFBP-AS1, 45 more genes
    nsv6684963copy number variation1nstd229human GRCh38 chr2: 218,333,116-218,389,815 , GRCh37.p13 chr2: 219,197,839-219,254,538 SLC11A1, CATIP-AS1, 5 more genes
    nsv6682539copy number variation1nstd229human GRCh38 chr2: 218,243,701-218,286,200 , GRCh37.p13 chr2: 219,108,424-219,150,923 TMBIM1, MIR6513, 5 more genes
    nsv6678705copy number variation1nstd229human GRCh38 chr2: 218,337,085-218,360,622 , GRCh37.p13 chr2: 219,201,808-219,225,345 RPL19P5, PNKD, 3 more genes
    nsv6554515inversion1nstd223human GRCh38 chr2: 218,309,765-218,310,305 , GRCh37.p13 chr2: 219,174,488-219,175,028 PNKD, LOC105373881
    nsv6542142inversion1nstd223human GRCh38 chr2: 218,296,778-218,297,685 , GRCh37.p13 chr2: 219,161,501-219,162,408 PNKD
    nsv6355557copy number variation1nstd223human GRCh38 chr2: 218,287,541-218,291,547 , GRCh37.p13 chr2: 219,152,264-219,156,270 TMBIM1, PNKD
    nsv6350590copy number variation1nstd223human GRCh38 chr2: 218,309,039-218,369,142 , GRCh37.p13 chr2: 219,173,762-219,233,865 PNKD, CATIP, 6 more genes
    nsv6349844copy number variation1nstd223human GRCh38 chr2: 218,315,341-218,319,175 , GRCh37.p13 chr2: 219,180,064-219,183,898 LOC105373880, PNKD, 1 more genes
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