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Items: 1 to 20 of 393

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7075760inversion1nstd229human GRCh38 chr19: 54,368,885-57,042,988 , GRCh37.p13 chr19: 55,595,687-57,554,356 ZSCAN5C, TMEM190, 137 more genes
    nsv7068983inversion1nstd229human GRCh38 chr19: 54,896,341-55,127,353 , GRCh37.p13 chr19|NW_004166865.1: 870,709-1,058,686 GP6-AS1, MIR7975, 8 more genes
    nsv7067331inversion1nstd229human GRCh38 chr19: 54,730,353-56,291,074 , GRCh37.p13 chr19: 55,595,687-56,802,443 NLRP2, KIR2DP1, 85 more genes
    nsv7064403inversion1nstd229human GRCh38 chr19: 55,044,292-55,044,333 , GRCh37.p13 chr19|NW_004166865.1: 1,018,660-1,018,701 RDH13
    nsv7063985inversion1nstd229human GRCh38 chr19: 54,915,834-55,058,786 , GRCh37.p13 chr19|NW_004166865.1: 890,202-1,033,154 NCR1, GP6, 5 more genes
    nsv7063630inversion1nstd229human GRCh38 chr19: 54,312,295-55,433,689 , GRCh37.p13 chr19|NW_004166865.1: 286,662-1,058,686 BRSK1, VN1R104P, 69 more genes
    nsv7062087inversion1nstd229human GRCh38 chr19: 54,368,882-57,042,981 , GRCh37.p13 chr19: 55,595,687-57,554,349 BRSK1, ZIM2, 137 more genes
    nsv7060532inversion1nstd229human GRCh38 chr19: 54,888,784-55,573,986 , GRCh37.p13 chr19: 55,595,687-56,085,352 SSC5D, MIR6804, 41 more genes
    nsv7060477inversion1nstd229human GRCh38 chr19: 54,915,805-55,057,436 , GRCh37.p13 chr19|NW_004166865.1: 890,173-1,031,804 RPL36AP50, GP6, 5 more genes
    nsv7059339inversion1nstd229human GRCh38 chr19: 54,925,072-55,050,053 , GRCh37.p13 chr19|NW_004166865.1: 899,440-1,024,421 NCR1, GP6, 5 more genes
    nsv7059172inversion1nstd229human GRCh38 chr19: 55,056,856-55,060,495 , GRCh37.p13 chr19|NW_004166865.1: 1,031,224-1,034,863 RDH13
    nsv7059060inversion1nstd229human GRCh38 chr19: 55,053,702-55,057,737 , GRCh37.p13 chr19|NW_004166865.1: 1,028,070-1,032,105 RDH13
    nsv7017714copy number variation1nstd229human GRCh38 chr19: 55,061,201-55,069,000 , GRCh37.p13 chr19|NW_004166865.1: 1,035,569-1,043,368 RDH13
    nsv7017299copy number variation1nstd229human GRCh38 chr19: 54,934,082-55,054,708 , GRCh37.p13 chr19|NW_004166865.1: 908,450-1,029,076 NCR1, NLRP7, 5 more genes
    nsv7015841copy number variation1nstd229human GRCh38 chr19: 55,068,239-55,068,808 , GRCh37.p13 chr19|NW_004166865.1: 1,042,607-1,043,176 RDH13
    nsv7014769copy number variation1nstd229human GRCh38 chr19: 55,018,959-55,148,797 , GRCh37.p13 chr19|NW_004166865.1: 993,327-1,058,686 MIR7975, TNNT1, 5 more genes
    nsv7013063copy number variation1nstd229human GRCh38 chr19: 55,064,676-55,065,781 , GRCh37.p13 chr19|NW_004166865.1: 1,039,044-1,040,149 RDH13
    nsv7011713copy number variation1nstd229human GRCh38 chr19: 54,880,948-55,059,715 , GRCh37.p13 chr19|NW_004166865.1: 855,316-1,034,083 NLRP2, RDH13, 6 more genes
    nsv7010062copy number variation1nstd229human GRCh38 chr19: 55,059,544-55,064,161 , GRCh37.p13 chr19|NW_004166865.1: 1,033,912-1,038,529 RDH13
    nsv7009346copy number variation1nstd229human GRCh38 chr19: 55,046,101-55,057,700 , GRCh37.p13 chr19|NW_004166865.1: 1,020,469-1,032,068 RDH13
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