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Items: 1 to 20 of 515

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099241copy number variation1nstd231human GRCh38.p12 chr1: 161,703,753-165,575,316 , GRCh37 chr1: 161,673,543-165,544,553 LMX1A, DDR2, 49 more genes
    nsv7057537inversion1nstd229human GRCh38 chr1: 161,493,525-166,518,262 , GRCh37.p13 chr1: 161,463,315-166,487,499 LOC107985451, ALDH9A1, 88 more genes
    nsv7048323inversion1nstd229human GRCh38 chr1: 163,200,695-163,200,783 , GRCh37.p13 chr1: 163,170,485-163,170,573 RGS5-AS1, RGS5
    nsv7043397inversion1nstd229human GRCh38 chr1: 163,317,150-163,318,906 , GRCh37.p13 chr1: 163,286,940-163,288,696 RGS5
    nsv7042802inversion1nstd229human GRCh38 chr1: 159,324,839-163,640,188 , GRCh37.p13 chr1: 159,294,629-163,609,919 TRG-GCC2-1, LOC107985220, 178 more genes
    nsv7039884inversion1nstd229human GRCh38 chr1: 159,817,036-167,858,499 , GRCh37.p13 chr1: 159,786,826-167,827,737 TRP-AGG2-1, FCGR2C, 228 more genes
    nsv6643657copy number variation1nstd229human GRCh38 chr1: 163,251,001-163,269,000 , GRCh37.p13 chr1: 163,220,791-163,238,790 RGS5
    nsv6643656copy number variation1nstd229human GRCh38 chr1: 163,226,186-163,226,214 , GRCh37.p13 chr1: 163,195,976-163,196,004 RGS5
    nsv6643653copy number variation1nstd229human GRCh38 chr1: 163,219,880-163,225,501 , GRCh37.p13 chr1: 163,189,670-163,195,291 RGS5
    nsv6643651copy number variation1nstd229human GRCh38 chr1: 163,177,036-163,189,982 , GRCh37.p13 chr1: 163,146,826-163,159,772 RGS5-AS1, RGS5
    nsv6643650copy number variation1nstd229human GRCh38 chr1: 163,171,006-163,171,747 , GRCh37.p13 chr1: 163,140,796-163,141,537 RGS5-AS1, RGS5
    nsv6643648copy number variation1nstd229human GRCh38 chr1: 163,147,501-163,152,547 , GRCh37.p13 chr1: 163,117,291-163,122,337 RGS5
    nsv6643620copy number variation1nstd229human GRCh38 chr1: 162,606,455-163,662,918 , GRCh37.p13 chr1: 162,576,245-163,632,647 RGS4, RGS5-AS1, 12 more genes
    nsv6643561copy number variation1nstd229human GRCh38 chr1: 163,287,957-163,312,299 , GRCh37.p13 chr1: 163,257,747-163,282,089 RGS5
    nsv6643560copy number variation1nstd229human GRCh38 chr1: 163,272,115-163,278,179 , GRCh37.p13 chr1: 163,241,905-163,247,969 RGS5
    nsv6643558copy number variation1nstd229human GRCh38 chr1: 163,217,381-163,226,052 , GRCh37.p13 chr1: 163,187,171-163,195,842 RGS5
    nsv6643557copy number variation1nstd229human GRCh38 chr1: 163,201,729-163,209,441 , GRCh37.p13 chr1: 163,171,519-163,179,231 RGS5, RGS5-AS1
    nsv6643556copy number variation1nstd229human GRCh38 chr1: 163,195,956-163,199,943 , GRCh37.p13 chr1: 163,165,746-163,169,733 RGS5-AS1, RGS5
    nsv6643555copy number variation1nstd229human GRCh38 chr1: 163,138,947-163,142,266 , GRCh37.p13 chr1: 163,108,737-163,112,056 RGS5
    nsv6643199copy number variation1nstd229human GRCh38 chr1: 163,285,084-163,341,171 , GRCh37.p13 chr1: 163,254,874-163,310,961 NUF2, RGS5
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