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Items: 1 to 20 of 107

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137133copy number variation1nstd102humanUncertain significance GRCh37 chr6: 159,006,336-170,713,678 , GRCh38.p12 chr6: 158,585,304-170,404,590 LOC101929460, GPR31, 199 more genes
    nsv7097050copy number variation2nstd102humanPathogenic GRCh37 chr6: 158,532,398-162,868,359 , GRCh38.p12 chr6: 158,111,366-162,447,327 LOC107986665, HNRNPH1P1, 64 more genes
    nsv7057653inversion1nstd229human GRCh38 chr6: 155,088,001-159,627,095 , GRCh37.p13 chr6: 155,409,135-160,048,127 SNORD28B, NMTRV-TAC1-1, 62 more genes
    nsv7053022inversion1nstd229human GRCh38 chr6: 153,431,159-160,785,697 , GRCh37.p13 chr6: 153,752,294-161,206,729 OPRM1, FNDC1-AS1, 106 more genes
    nsv7052273inversion1nstd229human GRCh38 chr6: 153,428,141-160,785,922 , GRCh37.p13 chr6: 153,749,276-161,206,954 LOC442272, CACYBPP3, 106 more genes
    nsv7050008inversion1nstd229human GRCh38 chr6: 153,421,054-160,785,901 , GRCh37.p13 chr6: 153,742,189-161,206,933 SLC22A2, IGF2R, 108 more genes
    nsv6816570copy number variation1nstd229human GRCh38 chr6: 159,133,367-159,632,143 , GRCh37.p13 chr6: 159,554,399-160,053,175 LINC02529, FNDC1, 5 more genes
    nsv6813463copy number variation1nstd229human GRCh38 chr6: 159,354,290-159,552,111 , GRCh37.p13 chr6: 159,775,322-159,973,143 LOC101929142, RPL21P69, 2 more genes
    nsv6813225copy number variation1nstd229human GRCh38 chr6: 159,325,010-159,409,310 , GRCh37.p13 chr6: 159,746,042-159,830,342 LINC02529, LOC105378084
    nsv6810510copy number variation1nstd229human GRCh38 chr6: 159,383,446-159,384,263 , GRCh37.p13 chr6: 159,804,478-159,805,295 LINC02529, LOC105378084
    nsv6804859copy number variation1nstd229human GRCh38 chr6: 159,379,478-159,386,885 , GRCh37.p13 chr6: 159,800,510-159,807,917 LOC105378084, LINC02529
    nsv6801502copy number variation1nstd229human GRCh38 chr6: 159,372,101-159,543,000 , GRCh37.p13 chr6: 159,793,133-159,964,032 RPL21P69, LOC105378084, 2 more genes
    nsv6634356copy number variation1nstd102humanPathogenic GRCh37 chr6: 157,318,401-165,233,548 , GRCh38.p12 chr6: 156,997,267-164,820,059 LOC105378097, LOC105378094, 103 more genes
    nsv6618794copy number variation1nstd223human GRCh38 chr6: 159,133,367-159,632,139 , GRCh37.p13 chr6: 159,554,399-160,053,171 LOC105378085, FNDC1, 5 more genes
    nsv6573818inversion1nstd223human GRCh38 chr6: 153,431,058-160,785,713 , GRCh37.p13 chr6: 153,752,193-161,206,745 MTRES1P1, SOD2-OT1, 106 more genes
    nsv6564527inversion1nstd223human GRCh38 chr6: 150,782,887-160,100,808 , GRCh37.p13 chr6: 151,104,023-160,521,840 RPL31P29, RPL17P24, 139 more genes
    nsv6562231inversion1nstd223human GRCh38 chr6: 150,783,018-160,100,808 , GRCh37.p13 chr6: 151,104,154-160,521,840 ARMT1, LOC102723831, 139 more genes
    nsv6558878inversion1nstd223human GRCh38 chr6: 153,428,103-160,785,918 , GRCh37.p13 chr6: 153,749,238-161,206,950 IGF2R, SOD2-OT1, 106 more genes
    nsv6315428copy number variation1nstd102humanPathogenic GRCh37 chr6: 159,121,459-170,919,482 , GRCh38.p12 chr6: 158,700,427-170,610,394 TBP, LOC105378130, 200 more genes
    nsv6313530copy number variation1nstd102humanPathogenic GRCh37 chr6: 153,207,930-164,322,346 , GRCh38.p12 chr6: 152,886,795-163,901,314 RSPH3, FBXO5, 144 more genes
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