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Items: 1 to 20 of 184

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7054037inversion1nstd229human GRCh38 chr5: 180,861,345-180,861,422 , GRCh37.p13 chr5: 180,288,345-180,288,422 ZFP62
    nsv7053423inversion1nstd229human GRCh38 chr5: 180,767,059-181,141,901 , GRCh37.p13 chr5: 180,194,059-180,568,901 HEIH, TRV-CAC1-3, 19 more genes
    nsv7045576inversion1nstd229human GRCh38 chr5: 180,805,627-181,281,045 , GRCh37.p13 chr5: 180,232,627-180,708,046 RPL13P10, TRV-AAC1-3, 46 more genes
    nsv7044540inversion1nstd229human GRCh38 chr5: 180,832,761-181,281,244 , GRCh37.p13 chr5: 180,259,761-180,708,245 LOC100128762, SNORD95, 44 more genes
    nsv6795222copy number variation1nstd229human GRCh38 chr5: 180,785,301-180,861,900 , GRCh37.p13 chr5: 180,212,301-180,288,900 ZFP62, LINC00847, 2 more genes
    nsv6794508copy number variation1nstd229human GRCh38 chr5: 180,858,454-180,858,884 , GRCh37.p13 chr5: 180,285,454-180,285,884 ZFP62
    nsv6794354copy number variation1nstd229human GRCh38 chr5: 180,767,201-180,890,800 , GRCh37.p13 chr5: 180,194,201-180,317,800 HEIH, ZFP62, 2 more genes
    nsv6791281copy number variation1nstd229human GRCh38 chr5: 180,572,466-180,861,055 , GRCh37.p13 chr5: 179,999,466-180,288,055 MGAT1, OR2Y1, 10 more genes
    nsv6784981copy number variation1nstd229human GRCh38 chr5: 180,850,968-181,155,283 , GRCh37.p13 chr5: 180,277,968-180,582,283 RNU6-1036P, LOC729707, 17 more genes
    nsv6784768copy number variation1nstd229human GRCh38 chr5: 180,843,594-180,844,724 , GRCh37.p13 chr5: 180,270,594-180,271,724 ZFP62
    nsv6636938copy number variation1nstd102humanUncertain significance GRCh37 chr5: 179,922,498-180,608,605 , GRCh38.p12 chr5: 180,495,498-181,181,605 RNU6-1036P, TRL-AAG7-1, 34 more genes
    nsv6636455copy number variation1nstd102humanUncertain significance GRCh37 chr5: 180,148,276-180,719,789 , GRCh38.p12 chr5: 180,721,276-181,292,788 OR2Y1, TRV-AAC1-2, 48 more genes
    nsv6634369copy number variation1nstd102humanPathogenic GRCh37 chr5: 170,350,336-180,719,789 , GRCh38.p12 chr5: 170,923,332-181,292,788 GFPT2, FOXO1B, 287 more genes
    nsv6407997copy number variation1nstd223human GRCh38 chr5: 180,719,401-181,088,900 , GRCh37.p13 chr5: 180,146,401-180,515,900 TMEM69P2, LOC100128762, 14 more genes
    nsv6407419copy number variation1nstd223human GRCh38 chr5: 180,603,826-181,165,321 , GRCh37.p13 chr5: 180,030,826-180,592,321 LINC02222, RNU1-17P, 28 more genes
    nsv6406595copy number variation1nstd223human GRCh38 chr5: 180,301,408-180,869,378 , GRCh37.p13 chr5: 179,728,408-180,296,378 LOC100329129, LINC02222, 14 more genes
    nsv6401030copy number variation1nstd223human GRCh38 chr5: 180,850,968-181,155,283 , GRCh37.p13 chr5: 180,277,968-180,582,283 TRV-CAC1-3, TMEM69P2, 17 more genes
    nsv6315448copy number variation1nstd102humanPathogenic GRCh37 chr5: 149,010,383-180,719,789 , GRCh38.p12 chr5: 149,630,820-181,292,788 GRM6, MIR1229, 554 more genes
    nsv6135205copy number variation1nstd213human GRCh37 chr5: 91,690,000-180,740,001 , GRCh38.p12 chr5: 92,354,293-181,313,000 ADRA1B, ASS1P10, 1378 more genes
    nsv6135164copy number variation1nstd213human GRCh37 chr5: 179,970,000-180,480,001 , GRCh38.p12 chr5: 180,543,000-181,053,001 MGAT1, SCGB3A1, 19 more genes
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