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Items: 1 to 20 of 128

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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
    nsv7067331inversion1nstd229human GRCh38 chr19: 54,730,353-56,291,074 , GRCh37.p13 chr19: 55,595,687-56,802,443 NLRP2, KIR2DP1, 85 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
    nsv7014954copy number variation1nstd229human GRCh38 chr19: 55,350,963-55,356,185 , GRCh37.p13 chr19: 55,862,331-55,867,553 COX6B2, GARIN5B
    nsv7014855copy number variation1nstd229human GRCh38 chr19: 55,312,701-55,384,200 , GRCh37.p13 chr19: 55,824,069-55,895,568 GARIN5B, IL11, 7 more genes
    nsv7005052copy number variation1nstd229human GRCh38 chr19: 55,227,001-55,384,200 , GRCh37.p13 chr19: 55,738,369-55,895,568 PPP6R1, GARIN5B, 13 more genes
    nsv7003652copy number variation1nstd229human GRCh38 chr19: 55,352,068-55,352,629 , GRCh37.p13 chr19: 55,863,436-55,863,997 COX6B2
    nsv6998458copy number variation1nstd229human GRCh38 chr19: 55,266,101-55,489,000 , GRCh37.p13 chr19: 55,777,469-56,000,367 TMEM150B, BRSK1, 17 more genes
    nsv6637813copy number variation1nstd102humanUncertain significance GRCh37 chr19: 55,642,778-55,932,200 , GRCh38.p12 chr19: 55,131,410-55,420,833 TMEM150B, TNNI3, 23 more genes
    nsv6596657inversion1nstd223human GRCh38 chr19: 54,888,785-55,573,993 , GRCh37.p13 chr19: 55,595,687-56,085,359 SBK2, BRSK1, 41 more genes
    nsv6529975copy number variation1nstd223human GRCh38 chr19: 55,307,661-55,545,550 , GRCh37.p13 chr19: 55,819,029-56,056,916 BRSK1, SBK2, 18 more genes
    nsv6516967copy number variation1nstd223human GRCh38 chr19: 55,332,147-55,405,383 , GRCh37.p13 chr19: 55,843,515-55,916,751 TMEM150B, RPL28, 9 more genes
    nsv6515862copy number variation1nstd223human GRCh38 chr19: 55,346,595-55,385,047 , GRCh37.p13 chr19: 55,857,963-55,896,415 TMEM190, GARIN5B, 5 more genes
    nsv6315178copy number variation1nstd102humanUncertain significance GRCh37 chr19: 55,434,660-56,463,734 , GRCh38.p12 chr19: 54,923,292-55,952,368 RDH13, SSC5D, 62 more genes
    nsv6306186copy number variation1nstd186human GRCh37 chr19: 55,856,242-55,862,242 , GRCh38.p12 chr19: 55,344,874-55,350,874 COX6B2, KMT5C
    nsv6291483copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 55,247,893-56,503,347 , GRCh38.p12 chr19: 54,911,986-55,991,981 IL11, PTPRH, 62 more genes
    nsv6229757insertion1nstd214human GRCh38 chr19: 55,354,273-55,354,273 , GRCh37.p13 chr19: 55,865,641-55,865,641 GARIN5B, COX6B2
    nsv6146485copy number variation1nstd206human GRCh38 chr19: 55,348,874-55,354,874 , GRCh37.p13 chr19: 55,860,242-55,866,242 GARIN5B, COX6B2
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