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Items: 1 to 20 of 335

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5428292copy number variation1nstd206human GRCh38 chrX: 17,798,390-17,798,803 , GRCh37.p13 chrX: 17,816,510-17,816,923 RAI2
    nsv5381747copy number variation5nstd102humanUncertain significance GRCh37 chrX: 17,393,881-20,284,750 , GRCh38.p12 chrX: 17,375,758-20,266,632 TMSB10P2, BLOC1S6P1, 37 more genes
    nsv5059968copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-56,457,794 , GRCh38.p12 chrX: 251,879-56,431,361 PAGE3, METTL15P3, 785 more genes
    nsv4779196copy number variation1nstd200human GRCh37 chrX: 17,857,694-17,858,277 , GRCh38.p12 chrX: 17,839,574-17,840,157 RAI2
    nsv4769248copy number variation1nstd201human GRCh37 chrX: 168,546-21,870,371 , GRCh38.p12 chrX: 251,879-21,852,253 , AMELX, 248 more genes
    nsv4728486copy number variation1nstd102humanPathogenic GRCh37 chrX: 219,609-55,466,476 , GRCh38.p12 chrX: 302,942-55,440,043 CDK16, WASF4P, 772 more genes
    nsv4674687copy number variation1nstd102humanUncertain significance GRCh37 chrX: 15,415,636-18,339,030 , GRCh38.p12 chrX: 15,397,514-18,320,910 ZRSR2, HNRNPDLP5, 45 more genes
    nsv4674655copy number variation1nstd102humanPathogenic GRCh37 chrX: 16,194,993-20,640,014 , GRCh38.p12 chrX: 16,176,870-20,621,896 LOC101928389, LOC729609, 54 more genes
    nsv4674615copy number variation1nstd102humanPathogenic GRCh37 chrX: 1,240,318-20,986,848 , GRCh38.p12 chrX: 1,140,165-20,968,730 RNA5SP499, GS1-600G8.3, 217 more genes
    nsv4674588copy number variation1nstd102humanPathogenic GRCh37 chrX: 539,722-55,509,385 , GRCh38.p12 chrX: 578,987-55,482,952 LOC392440, SSX4, 769 more genes
    nsv4674458copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-34,753,512 , GRCh38.p12 chrX: 251,879-34,735,395 P2RY8, CA5BP1-CA5B, 344 more genes
    nsv4674282copy number variation1nstd102humanPathogenic GRCh37 chrX: 537,158-22,883,547 , GRCh38.p12 chrX: 576,423-22,865,430 NHS, EGFL6, 236 more genes
    nsv4577397mobile element insertion1nstd166human GRCh37.p13 chrX: 17,863,054-17,863,054 , GRCh38.p12 chrX: 17,844,934-17,844,934 RAI2
    nsv4454863copy number variation1nstd102humanUncertain significance GRCh37 chrX: 17,557,444-19,260,546 , GRCh38.p12 chrX: 17,539,322-19,242,428 CDKL5, NHS-AS1, 24 more genes
    nsv4454842copy number variation1nstd102humanPathogenic GRCh37 chrX: 2,190,434-23,795,839 , GRCh38.p12 chrX: 2,272,393-23,777,722 MBTPS2, LOC101928389, 224 more genes
    nsv4454143copy number variation1nstd102humanPathogenic GRCh37 chrX: 15,330,714-21,915,234 , GRCh38.p12 chrX: 15,312,592-21,897,116 LOC105373146, ZRSR2, 83 more genes
    nsv4452472copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-61,877,279 , GRCh38.p12 chrX: 251,879-62,657,809 MIR660, RNU6-1321P, 802 more genes
    nsv4452333copy number variation2nstd102humanPathogenic GRCh37 chrX: 13,962,918-22,148,232 , GRCh38.p12 chrX: 13,944,799-22,130,115 SETP15, RNU5F-7P, 96 more genes
    nsv4451246copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-38,054,739 , GRCh38.p12 chrX: 251,879-38,195,486 H3P43, CA5B, 381 more genes
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