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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5369036translocation1nstd200human GRCh38 chr5: 160,479,390-160,479,390 , GRCh38 chr5: 160,483,381-160,483,381 , GRCh37.p13 chr5: 159,910,388-159,910,388 , GRCh37.p13 chr5: 159,906,397-159,906,397 MIR3142HG, MIR146A
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv4939541copy number variation1nstd200human GRCh38 chr5: 160,482,848-160,485,026 , GRCh37.p13 chr5: 159,909,855-159,912,033 MIR3142HG, MIR146A
    nsv4939540copy number variation1nstd200human GRCh38 chr5: 160,479,374-160,483,380 , GRCh37.p13 chr5: 159,906,381-159,910,387 MIR3142HG, MIR146A
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4815221copy number variation1nstd200human GRCh37 chr5: 159,912,879-159,913,348 , GRCh38.p12 chr5: 160,485,872-160,486,341 MIR146A, MIR3142HG
    nsv4676086copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 159,714,197-161,313,217 , GRCh38.p12 chr5: 160,287,190-161,886,211 GABRA1, GABRA6, 16 more genes
    nsv4675397copy number variation1nstd102humanPathogenic GRCh37 chr5: 157,801,321-162,780,186 , GRCh38.p12 chr5: 158,374,313-163,353,180 MIR146A, SNRPEP1, 52 more genes
    nsv4674945copy number variation1nstd102humanPathogenic GRCh37 chr5: 156,347,980-169,959,880 , GRCh38.p12 chr5: 156,920,969-170,532,876 LINC02227, LINC01932, 146 more genes
    nsv4674838copy number variation1nstd102humanUncertain significance GRCh37 chr5: 159,623,973-160,000,962 , GRCh38.p12 chr5: 160,196,966-160,573,955 PTTG1, SNRPEP1, 12 more genes
    nsv4455586copy number variation1nstd102humanPathogenic GRCh37 chr5: 156,597,181-171,166,353 , GRCh38.p12 chr5: 157,170,170-171,739,349 LOC105377677, GABRA6, 164 more genes
    nsv4126056copy number variation1nstd166human GRCh37.p13 chr5: 159,698,170-166,152,496 , GRCh38.p12 chr5: 160,271,163-166,725,491 , MIR3142, 49 more genes
    nsv3924400copy number variation1nstd102humanPathogenic NCBI36 chr5: 156,185,101-180,629,412 , GRCh37 chr5: 156,252,523-180,696,806 , GRCh38 chr5: 156,825,512-181,269,805 CEP192P1, ARL2BPP6, 443 more genes
    nsv3922783copy number variation1nstd102humanPathogenic GRCh38 chr5: 152,761,187-167,248,053 , NCBI36 chr5: 152,120,940-166,607,636 , GRCh37 chr5: 152,140,747-166,675,058 APOOP1, LOC102724458, 151 more genes
    nsv3921182copy number variation1nstd102humanPathogenic GRCh37 chr5: 149,094,155-180,699,152 , GRCh38 chr5: 149,714,592-181,272,151 , NCBI36 chr5: 149,074,348-180,631,758 RN7SKP148, TCOF1, 553 more genes
    nsv3915958copy number variation1nstd102humanPathogenic GRCh38 chr5: 152,443,869-166,104,392 , NCBI36 chr5: 151,803,623-165,463,975 , GRCh37 chr5: 151,823,430-165,531,397 C5orf52, FAM114A2, 147 more genes
    nsv3915259copy number variation1nstd102humanPathogenic GRCh37 chr5: 158,368,362-163,813,766 , NCBI36 chr5: 158,300,940-163,746,344 , GRCh38 chr5: 158,941,354-164,386,760 ATP10B, LINC01845, 61 more genes
    nsv3914878copy number variation1nstd102humanPathogenic NCBI36 chr5: 146,520,648-163,194,778 , GRCh37.p13 chr5: 146,540,455-163,262,200 , GRCh38.p12 chr5: 147,160,892-163,835,194 LOC105378231, RN7SKP232, 247 more genes
    nsv3912593copy number variation1nstd102humanUncertain significance NCBI36 chr5: 332,389-180,837,866 , GRCh37.p13 chr5: 279,389-180,905,260 , GRCh38.p12 chr5: 279,274-181,478,259 LOC105378993, LOC107986375, 2492 more genes
    nsv3889848copy number variation1nstd102humanPathogenic GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719 MEGF10, LOC100128407, 2080 more genes
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