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Items: 1 to 20 of 164

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057970inversion1nstd229human GRCh38 chr5: 39,369,727-42,623,585 , GRCh37.p13 chr5: 39,369,829-42,623,687 LINC02996, DAB2, 36 more genes
    nsv7047645inversion1nstd229human GRCh38 chr5: 41,406,025-41,420,935 , GRCh37.p13 chr5: 41,406,127-41,421,037 LOC105374740, PLCXD3
    nsv7042577inversion1nstd229human GRCh38 chr5: 41,026,178-41,542,329 , GRCh37.p13 chr5: 41,026,280-41,542,431 C6, MROH2B, 4 more genes
    nsv7041157inversion1nstd229human GRCh38 chr5: 40,200,630-42,327,400 , GRCh37.p13 chr5: 40,200,732-42,327,502 RNU7-161P, LINC02996, 26 more genes
    nsv6777724copy number variation1nstd229human GRCh38 chr5: 41,391,193-41,391,286 , GRCh37.p13 chr5: 41,391,295-41,391,388 LOC105374740, PLCXD3
    nsv6769814copy number variation1nstd229human GRCh38 chr5: 39,447,462-42,528,554 , GRCh37.p13 chr5: 39,447,564-42,528,656 RNU7-161P, OXCT1, 35 more genes
    nsv6766084copy number variation1nstd229human GRCh38 chr5: 41,393,200-41,398,125 , GRCh37.p13 chr5: 41,393,302-41,398,227 PLCXD3, LOC105374740
    nsv6765910copy number variation1nstd229human GRCh38 chr5: 41,405,122-41,407,755 , GRCh37.p13 chr5: 41,405,224-41,407,857 LOC105374740, PLCXD3
    nsv6765158copy number variation1nstd229human GRCh38 chr5: 41,401,784-41,402,470 , GRCh37.p13 chr5: 41,401,886-41,402,572 PLCXD3, LOC105374740
    nsv6764078copy number variation1nstd229human GRCh38 chr5: 41,382,372-41,396,991 , GRCh37.p13 chr5: 41,382,474-41,397,093 PLCXD3, LOC105374740
    nsv6636973copy number variation1nstd102humanPathogenic GRCh37 chr5: 29,348,753-46,389,339 , GRCh38.p12 chr5: 29,348,646-46,389,237 SUB1, LOC105374740, 210 more genes
    nsv6575329inversion1nstd223human GRCh38 chr5: 41,394,251-41,394,342 , GRCh37.p13 chr5: 41,394,353-41,394,444 LOC105374740, PLCXD3
    nsv6573070inversion1nstd223human GRCh38 chr5: 41,406,025-41,420,935 , GRCh37.p13 chr5: 41,406,127-41,421,037 PLCXD3, LOC105374740
    nsv6395581copy number variation1nstd223human GRCh38 chr5: 41,385,780-41,386,381 , GRCh37.p13 chr5: 41,385,882-41,386,483 PLCXD3, LOC105374740
    nsv6393867copy number variation1nstd223human GRCh38 chr5: 41,402,101-41,402,800 , GRCh37.p13 chr5: 41,402,203-41,402,902 PLCXD3, LOC105374740
    nsv6389209copy number variation1nstd223human GRCh38 chr5: 41,382,372-41,396,987 , GRCh37.p13 chr5: 41,382,474-41,397,089 PLCXD3, LOC105374740
    nsv6388671copy number variation1nstd223human GRCh38 chr5: 39,447,462-42,528,554 , GRCh37.p13 chr5: 39,447,564-42,528,656 SERBP1P6, TCP1P2, 35 more genes
    nsv6378891copy number variation1nstd223human GRCh38 chr5: 41,389,682-41,390,042 , GRCh37.p13 chr5: 41,389,784-41,390,144 PLCXD3, LOC105374740
    nsv6376255copy number variation1nstd223human GRCh38 chr5: 41,406,644-41,407,149 , GRCh37.p13 chr5: 41,406,746-41,407,251 PLCXD3, LOC105374740
    nsv6315368copy number variation1nstd102humanPathogenic GRCh37 chr5: 36,053,583-46,389,339 , GRCh38.p12 chr5: 36,053,481-46,389,237 C7, RIMOC1, 128 more genes
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