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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098859copy number variation1nstd102humanUncertain significance GRCh37 chr4: 169,669,584-172,013,457 , GRCh38.p12 chr4: 168,748,433-171,092,306 RNY4P17, LOC105377529, 27 more genes
    nsv7097242copy number variation1nstd102humanLikely pathogenic GRCh37 chr4: 170,482,611-170,483,367 , GRCh38.p12 chr4: 169,561,460-169,562,216 NEK1
    nsv7096843copy number variation1nstd102humanUncertain significance GRCh37 chr4: 170,482,611-170,523,781 , GRCh38.p12 chr4: 169,561,460-169,602,630 NEK1
    nsv7096842copy number variation1nstd102humanPathogenic GRCh37 chr4: 169,433,478-170,523,781 , GRCh38.p12 chr4: 168,512,327-169,602,630 RNU6-853P, SH3RF1, 14 more genes
    nsv7057820inversion1nstd229human GRCh38 chr4: 169,433,479-169,446,061 , GRCh37.p13 chr4: 170,354,630-170,367,212 NEK1
    nsv7057078inversion1nstd229human GRCh38 chr4: 169,248,940-169,514,277 , GRCh37.p13 chr4: 170,170,091-170,435,428 SH3RF1, LOC105377529, 1 more genes
    nsv7056217inversion1nstd229human GRCh38 chr4: 166,607,935-172,500,612 , GRCh37.p13 chr4: 167,529,086-173,421,763 DDX60, LOC105377529, 50 more genes
    nsv7052667inversion1nstd229human GRCh38 chr4: 169,479,838-169,486,041 , GRCh37.p13 chr4: 170,400,989-170,407,192 NEK1
    nsv7047158inversion1nstd229human GRCh38 chr4: 169,433,982-169,544,143 , GRCh37.p13 chr4: 170,355,133-170,465,294 NEK1
    nsv7046092inversion1nstd229human GRCh38 chr4: 169,526,682-169,530,753 , GRCh37.p13 chr4: 170,447,833-170,451,904 NEK1
    nsv7043365inversion1nstd229human GRCh38 chr4: 169,526,680-169,534,400 , GRCh37.p13 chr4: 170,447,831-170,455,551 NEK1
    nsv6757636copy number variation1nstd229human GRCh38 chr4: 169,486,324-169,523,263 , GRCh37.p13 chr4: 170,407,475-170,444,414 NEK1
    nsv6757430copy number variation1nstd229human GRCh38 chr4: 169,561,409-169,638,984 , GRCh37.p13 chr4: 170,482,560-170,560,135 CLCN3, NEK1
    nsv6756655copy number variation1nstd229human GRCh38 chr4: 169,462,982-169,474,667 , GRCh37.p13 chr4: 170,384,133-170,395,818 NEK1
    nsv6755981copy number variation1nstd229human GRCh38 chr4: 169,483,645-169,483,859 , GRCh37.p13 chr4: 170,404,796-170,405,010 NEK1
    nsv6755802copy number variation1nstd229human GRCh38 chr4: 169,450,701-169,455,300 , GRCh37.p13 chr4: 170,371,852-170,376,451 NEK1
    nsv6754434copy number variation1nstd229human GRCh38 chr4: 169,389,832-169,393,916 , GRCh37.p13 chr4: 170,310,983-170,315,067 NEK1
    nsv6754057copy number variation1nstd229human GRCh38 chr4: 169,422,401-169,436,700 , GRCh37.p13 chr4: 170,343,552-170,357,851 NEK1
    nsv6753806copy number variation1nstd229human GRCh38 chr4: 169,524,767-169,530,875 , GRCh37.p13 chr4: 170,445,918-170,452,026 NEK1
    nsv6753296copy number variation1nstd229human GRCh38 chr4: 169,387,043-169,397,391 , GRCh37.p13 chr4: 170,308,194-170,318,542 NEK1
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