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Items: 1 to 20 of 178

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148088copy number variation1nstd102humanUncertain significance GRCh37 chr17: 25,263,507-27,829,791 , GRCh38.p12 chr17: 26,936,481-29,502,773 RNU4-34P, RNU6-711P, 95 more genes
    nsv7095084copy number variation1nstd102humanUncertain significance GRCh37 chr17: 26,684,694-29,701,173 , GRCh38.p12 chr17: 28,357,671-31,374,155 RNU6-1267P, PIPOX, 114 more genes
    nsv7094962copy number variation1nstd102humanUncertain significance GRCh37 chr17: 26,684,694-27,581,367 , GRCh38.p12 chr17: 28,357,671-29,254,349 FLOT2, SPAG5-AS1, 50 more genes
    nsv7062182inversion1nstd229human GRCh38 chr17: 27,487,612-31,414,648 , GRCh37.p13 chr17: 25,814,638-29,741,666 ERAL1, SARM1, 140 more genes
    nsv6995753copy number variation1nstd229human GRCh38 chr17: 28,929,052-28,930,915 , GRCh37.p13 chr17: 27,256,070-27,257,933 LOC101927018, PHF12
    nsv6981917copy number variation1nstd229human GRCh38 chr17: 28,805,032-28,929,082 , GRCh37.p13 chr17: 27,132,050-27,256,100 MIR451A, FAM222B, 8 more genes
    nsv6978294copy number variation1nstd229human GRCh38 chr17: 28,938,989-28,971,764 , GRCh37.p13 chr17: 27,266,007-27,298,782 SEZ6, PHF12, 2 more genes
    nsv6498281copy number variation1nstd223human GRCh38 chr17: 28,888,293-28,925,540 , GRCh37.p13 chr17: 27,215,311-27,252,558 LOC101927018, FLOT2, 2 more genes
    nsv6314042copy number variation1nstd102humanPathogenic GRCh37 chr17: 21,690,653-28,281,232 , GRCh38.p12 chr17: 22,164,047-29,954,214 TAOK1, TNFAIP1, 131 more genes
    nsv6133232copy number variation1nstd213human GRCh37 chr17: 26,970,000-27,750,001 , GRCh38.p12 chr17: 28,642,982-29,422,983 CRYBA1, FLOT2, 37 more genes
    nsv6133229copy number variation1nstd213human GRCh37 chr17: 25,300,000-32,120,001 , GRCh38.p12 chr17: 26,972,974-33,792,982 BLMH, CPD, 197 more genes
    nsv6133228copy number variation1nstd213human GRCh37 chr17: 25,300,000-27,290,001 , GRCh38.p12 chr17: 26,972,974-28,962,983 LGALS9, RPL23A, 82 more genes
    nsv5709876mobile element insertion2nstd211human GRCh38 chr17: 28,912,071-28,912,071 , GRCh37.p13 chr17: 27,239,089-27,239,089 PHF12
    nsv5645374insertion1nstd207human GRCh38 chr17: 28,923,162-28,923,162 , GRCh37.p13 chr17: 27,250,180-27,250,180 PHF12
    nsv5432672mobile element insertion1nstd206human GRCh38 chr17: 28,912,071-28,912,122 , GRCh37.p13 chr17: 27,239,089-27,239,140 PHF12
    nsv5358778translocation1nstd200human GRCh38 chr17: 28,918,742-28,918,742 , GRCh38 chr17: 28,918,236-28,918,236 , GRCh37.p13 chr17: 27,245,760-27,245,760 , GRCh37.p13 chr17: 27,245,254-27,245,254 PHF12
    nsv5298255copy number variation1nstd204human GRCh38.p13 chr17: 28,914,739-28,916,738 , GRCh37.p13 chr17: 27,241,757-27,243,756 PHF12
    nsv5154969mobile element insertion1nstd203human GRCh38 chr17: 28,912,057-28,912,071 , GRCh37.p13 chr17: 27,239,075-27,239,089 PHF12
    nsv5140318mobile element insertion1nstd203human GRCh38 chr17: 28,915,063-28,915,078 , GRCh37.p13 chr17: 27,242,081-27,242,096 PHF12
    nsv5023917copy number variation1nstd200human GRCh38 chr17: 28,904,662-28,909,207 , GRCh37.p13 chr17: 27,231,680-27,236,225 PHF12
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