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Items: 1 to 20 of 297

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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
    nsv5418344copy number variation1nstd206human GRCh38 chrX: 18,849,171-19,630,885 , GRCh37.p13 chrX: 18,867,289-19,649,003 SH3KBP1, PDHA1, 8 more genes
    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
    nsv4779217copy number variation1nstd200human GRCh37 chrX: 18,929,736-18,934,543 , GRCh38.p12 chrX: 18,911,618-18,916,425 PHKA2, RN7SL48P
    nsv4769248copy number variation1nstd201human GRCh37 chrX: 168,546-21,870,371 , GRCh38.p12 chrX: 251,879-21,852,253 , AMELX, 248 more genes
    nsv4728724copy number variation1nstd102humanUncertain significance GRCh37 chrX: 18,922,539-19,243,013 , GRCh38.p12 chrX: 18,904,421-19,224,895 ADGRG2, LOC101928415, 2 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
    nsv4728284copy number variation1nstd102humanUncertain significance GRCh37 chrX: 18,582,617-19,417,295 , GRCh38.p12 chrX: 18,564,497-19,399,177 MAP3K15, ADGRG2, 12 more genes
    nsv4683242copy number variation2nstd102humanPathogenic GRCh37 chrX: 18,660,114-19,377,781 , GRCh38.p12 chrX: 18,641,994-19,359,663 RS1, RN7SL48P, 12 more genes
    nsv4680867copy number variation1nstd189human GRCh37.p13 chrX: 18,662,633-19,449,407 , GRCh38.p12 chrX: 18,644,513-19,431,289 PDHA1, PHKA2, 12 more genes
    nsv4680601copy number variation1nstd189human GRCh37.p13 chrX: 18,759,932-19,266,084 , GRCh38.p12 chrX: 18,741,814-19,247,966 PHKA2, PPEF1, 6 more genes
    nsv4680356copy number variation1nstd189human GRCh37.p13 chrX: 18,724,444-19,288,007 , GRCh38.p12 chrX: 18,706,325-19,269,889 PHKA2, PPEF1, 6 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
    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
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