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Items: 1 to 20 of 364

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148092copy number variation1nstd102humanPathogenic GRCh37 chr15: 75,165,490-102,520,892 , GRCh38.p12 chr15: 74,873,149-101,980,689 RPL9P8, COMMD4P1, 547 more genes
    nsv7137114copy number variation1nstd102humanPathogenic GRCh37 chr15: 98,996,113-101,211,899 , GRCh38.p12 chr15: 98,452,884-100,671,694 PGPEP1L, LOC105371017, 36 more genes
    nsv7098892copy number variation1nstd102humanPathogenic GRCh37 chr15: 84,228,005-102,264,590 , GRCh38.p12 chr15: 83,559,253-101,724,387 CIB1, RPS12P26, 326 more genes
    nsv7075901inversion1nstd229human GRCh38 chr15: 99,795,287-101,786,621 , GRCh37.p13 chr15: 100,335,492-102,326,824 GOLGA8VP, DNM1P46, 39 more genes
    nsv7074837inversion1nstd229human GRCh38 chr15: 98,618,777-101,109,346 , GRCh37.p13 chr15: 99,162,006-101,649,551 LOC440313, PRKXP1, 42 more genes
    nsv7072319inversion1nstd229human GRCh38 chr15: 99,798,704-101,768,404 , GRCh37.p13 chr15: 100,338,909-102,308,607 ADAMTS17, TARS3, 37 more genes
    nsv7071630inversion1nstd229human GRCh38 chr15: 99,746,792-101,514,499 , GRCh37.p13 chr15: 100,286,997-102,054,702 RN7SL484P, ALDH1A3, 32 more genes
    nsv7066127inversion1nstd229human GRCh38 chr15: 100,576,888-100,675,798 , GRCh37.p13 chr15: 101,117,093-101,216,003 LINS1, ASB7, 1 more genes
    nsv7065226inversion1nstd229human GRCh38 chr15: 98,338,625-100,843,802 , GRCh37.p13 chr15: 98,881,854-101,384,007 LOC102723335, LUNAR1, 39 more genes
    nsv7064682inversion1nstd229human GRCh38 chr15: 99,334,911-100,692,064 , GRCh37.p13 chr15: 99,875,116-101,232,269 LOC400464, LOC105371020, 24 more genes
    nsv7059511inversion1nstd229human GRCh38 chr15: 99,784,046-101,789,074 , GRCh37.p13 chr15: 100,324,251-102,329,277 RNA5SP402, TM2D3, 40 more genes
    nsv6977657copy number variation1nstd229human GRCh38 chr15: 100,373,283-100,781,018 , GRCh37.p13 chr15: 100,913,488-101,321,223 LOC105371024, RNU6-181P, 8 more genes
    nsv6975567copy number variation1nstd229human GRCh38 chr15: 100,567,263-100,567,361 , GRCh37.p13 chr15: 101,107,468-101,107,566 LINS1
    nsv6970396copy number variation1nstd229human GRCh38 chr15: 100,572,953-100,577,793 , GRCh37.p13 chr15: 101,113,158-101,117,998 LINS1
    nsv6970311copy number variation1nstd229human GRCh38 chr15: 100,585,078-100,585,338 , GRCh37.p13 chr15: 101,125,283-101,125,543 LINS1
    nsv6967100copy number variation1nstd229human GRCh38 chr15: 100,599,501-100,694,800 , GRCh37.p13 chr15: 101,139,706-101,235,005 LOC100419174, LINS1, 1 more genes
    nsv6637683copy number variation1nstd102humanPathogenic GRCh37 chr15: 77,512,817-102,035,027 , GRCh38.p12 chr15: 77,220,475-101,494,824 LINC02253, LOC107984790, 463 more genes
    nsv6637368copy number variation1nstd102humanUncertain significance GRCh37 chr15: 100,921,195-101,144,913 , GRCh38.p12 chr15: 100,380,990-100,604,708 CERS3-AS1, LOC102723335, 6 more genes
    nsv6635795copy number variation1nstd227human GRCh38.p12 chr15: 100,598,177-100,884,271 , GRCh37 chr15: 101,138,382-101,424,476 ALDH1A3, LINS1, 6 more genes
    nsv6593771inversion1nstd223human GRCh38 chr15: 99,795,890-101,768,715 , GRCh37.p13 chr15: 100,336,095-102,308,918 LOC107987228, SPATA41, 37 more genes
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