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Items: 1 to 20 of 564

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099200copy number variation1nstd231human GRCh38.p12 chr1: 48,332,143-48,859,618 , GRCh37 chr1: 48,797,815-49,325,290 SPATA6, BEND5, 5 more genes
    nsv7099199copy number variation1nstd231human GRCh38.p12 chr1: 47,175,123-48,269,119 , GRCh37 chr1: 47,640,795-48,734,791 FOXE3, FOXD2, 17 more genes
    nsv7057932inversion1nstd229human GRCh38 chr1: 48,394,984-48,479,828 , GRCh37.p13 chr1: 48,860,656-48,945,500 RNU4-61P, SPATA6, 1 more genes
    nsv7052650inversion1nstd229human GRCh38 chr1: 47,584,744-54,395,558 , GRCh37.p13 chr1: 48,050,416-54,861,231 ANAPC10P1, SPATA6, 137 more genes
    nsv7050558inversion1nstd229human GRCh38 chr1: 48,116,108-48,813,202 , GRCh37.p13 chr1: 48,581,780-49,278,874 RPL21P25, SKINT1L, 9 more genes
    nsv7042666inversion1nstd229human GRCh38 chr1: 48,457,197-48,501,461 , GRCh37.p13 chr1: 48,922,869-48,967,133 SPATA6, RPL21P25
    nsv6651038copy number variation1nstd229human GRCh38 chr1: 48,340,510-48,345,915 , GRCh37.p13 chr1: 48,806,182-48,811,587 RNU6-723P, SPATA6
    nsv6651037copy number variation1nstd229human GRCh38 chr1: 48,330,999-48,334,828 , GRCh37.p13 chr1: 48,796,671-48,800,500 SPATA6
    nsv6651036copy number variation1nstd229human GRCh38 chr1: 48,304,266-48,352,177 , GRCh37.p13 chr1: 48,769,938-48,817,849 RNU6-723P, PPP1R8P1, 1 more genes
    nsv6651035copy number variation1nstd229human GRCh38 chr1: 48,244,280-48,257,509 , GRCh37.p13 chr1: 48,709,952-48,723,181 SPATA6, SLC5A9
    nsv6650974copy number variation1nstd229human GRCh38 chr1: 48,472,126-48,482,505 , GRCh37.p13 chr1: 48,937,798-48,948,177 SPATA6
    nsv6650973copy number variation1nstd229human GRCh38 chr1: 48,442,001-48,447,400 , GRCh37.p13 chr1: 48,907,673-48,913,072 SPATA6, RNU4-61P
    nsv6650972copy number variation1nstd229human GRCh38 chr1: 48,416,036-48,432,889 , GRCh37.p13 chr1: 48,881,708-48,898,561 SPATA6
    nsv6650968copy number variation1nstd229human GRCh38 chr1: 48,340,805-48,349,308 , GRCh37.p13 chr1: 48,806,477-48,814,980 RNU6-723P, SPATA6
    nsv6650967copy number variation1nstd229human GRCh38 chr1: 48,339,435-48,368,473 , GRCh37.p13 chr1: 48,805,107-48,834,145 RNU6-723P, SPATA6
    nsv6650966copy number variation1nstd229human GRCh38 chr1: 48,325,451-48,325,610 , GRCh37.p13 chr1: 48,791,123-48,791,282 PPP1R8P1, SPATA6
    nsv6650965copy number variation1nstd229human GRCh38 chr1: 48,276,809-48,415,801 , GRCh37.p13 chr1: 48,742,481-48,881,473 RNU6-723P, PPP1R8P1, 1 more genes
    nsv6650964copy number variation1nstd229human GRCh38 chr1: 48,273,301-48,283,400 , GRCh37.p13 chr1: 48,738,973-48,749,072 SPATA6
    nsv6650961copy number variation1nstd229human GRCh38 chr1: 48,256,442-48,256,985 , GRCh37.p13 chr1: 48,722,114-48,722,657 SPATA6
    nsv6650960copy number variation1nstd229human GRCh38 chr1: 48,256,042-48,258,000 , GRCh37.p13 chr1: 48,721,714-48,723,672 SPATA6
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