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Items: 1 to 20 of 409

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148175copy number variation1nstd102humanPathogenic GRCh38 chr1: 230,178,121-243,646,135 , GRCh37.p13 chr1: 230,313,867-243,809,437 AGT, MAP10, 221 more genes
    nsv7148158copy number variation1nstd102humanPathogenic GRCh38 chr1: 235,215,476-247,005,888 , GRCh37.p13 chr1: 235,378,791-247,169,190 RNU6-747P, LINC01139, 172 more genes
    nsv7093371copy number variation1nstd102humannot provided GRCh37 chr1: 224,230,307-243,181,599 , GRCh38.p12 chr1: 224,042,605-243,018,297 RPL36P6, MTND4LP21, 377 more genes
    nsv7054497inversion1nstd229human GRCh38 chr1: 236,163,834-236,170,703 , GRCh37.p13 chr1: 236,327,134-236,334,003 GPR137B
    nsv7053575inversion1nstd229human GRCh38 chr1: 236,166,764-236,186,364 , GRCh37.p13 chr1: 236,330,064-236,349,664 GPR137B
    nsv7051244inversion1nstd229human GRCh38 chr1: 236,179,957-236,180,064 , GRCh37.p13 chr1: 236,343,257-236,343,364 GPR137B
    nsv7044547inversion1nstd229human GRCh38 chr1: 234,053,817-240,091,334 , GRCh37.p13 chr1: 234,189,563-240,254,634 RNU6-725P, RNU6-968P, 101 more genes
    nsv7041309inversion1nstd229human GRCh38 chr1: 236,186,969-236,193,605 , GRCh37.p13 chr1: 236,350,269-236,356,905 GPR137B
    nsv7040505inversion1nstd229human GRCh38 chr1: 235,226,873-236,268,697 , GRCh37.p13 chr1: 235,390,188-236,431,997 RPS21P1, NID1, 26 more genes
    nsv6677584copy number variation1nstd229human GRCh38 chr1: 236,211,825-236,216,028 , GRCh37.p13 chr1: 236,375,125-236,379,328 ERO1B, GPR137B
    nsv6673765copy number variation1nstd229human GRCh38 chr1: 236,135,538-236,147,294 , GRCh37.p13 chr1: 236,298,838-236,310,594 GPR137B
    nsv6673582copy number variation1nstd229human GRCh38 chr1: 236,198,601-236,235,600 , GRCh37.p13 chr1: 236,361,901-236,398,900 GPR137B, ERO1B
    nsv6671415copy number variation1nstd229human GRCh38 chr1: 236,208,498-236,208,715 , GRCh37.p13 chr1: 236,371,798-236,372,015 GPR137B
    nsv6669652copy number variation1nstd229human GRCh38 chr1: 236,179,540-236,186,968 , GRCh37.p13 chr1: 236,342,840-236,350,268 GPR137B
    nsv6669535copy number variation1nstd229human GRCh38 chr1: 236,199,575-236,202,753 , GRCh37.p13 chr1: 236,362,875-236,366,053 GPR137B
    nsv6669086copy number variation1nstd229human GRCh38 chr1: 236,178,821-236,566,887 , GRCh37.p13 chr1: 236,342,121-236,730,187 LGALS8, LGALS8-AS1, 7 more genes
    nsv6668781copy number variation1nstd229human GRCh38 chr1: 236,158,620-236,168,075 , GRCh37.p13 chr1: 236,321,920-236,331,375 GPR137B
    nsv6667860copy number variation1nstd229human GRCh38 chr1: 236,198,913-236,207,204 , GRCh37.p13 chr1: 236,362,213-236,370,504 GPR137B
    nsv6666206copy number variation1nstd229human GRCh38 chr1: 236,166,461-236,166,539 , GRCh37.p13 chr1: 236,329,761-236,329,839 GPR137B
    nsv6666205copy number variation1nstd229human GRCh38 chr1: 236,169,401-236,173,300 , GRCh37.p13 chr1: 236,332,701-236,336,600 GPR137B
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