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Items: 1 to 20 of 468

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095086copy number variation1nstd102humanPathogenic GRCh37 chr17: 27,573,882-29,576,157 , GRCh38.p12 chr17: 29,246,864-31,249,139 LOC107984990, ADAP2, 59 more genes
    nsv7095084copy number variation1nstd102humanUncertain significance GRCh37 chr17: 26,684,694-29,701,173 , GRCh38.p12 chr17: 28,357,671-31,374,155 RNU6-1267P, PIPOX, 114 more genes
    nsv7077435inversion1nstd229human GRCh38 chr17: 30,077,121-30,079,554 , GRCh37.p13 chr17: 28,404,139-28,406,572 EFCAB5
    nsv7075227inversion1nstd229human GRCh38 chr17: 30,081,004-30,083,288 , GRCh37.p13 chr17: 28,408,022-28,410,306 EFCAB5
    nsv7065542inversion1nstd229human GRCh38 chr17: 29,976,918-29,977,009 , GRCh37.p13 chr17: 28,303,936-28,304,027 EFCAB5
    nsv7062182inversion1nstd229human GRCh38 chr17: 27,487,612-31,414,648 , GRCh37.p13 chr17: 25,814,638-29,741,666 ERAL1, SARM1, 140 more genes
    nsv7060914inversion1nstd229human GRCh38 chr17: 30,053,626-30,060,916 , GRCh37.p13 chr17: 28,380,644-28,387,934 RNY4P13, EFCAB5
    nsv7059192inversion1nstd229human GRCh38 chr17: 30,069,297-30,546,697 , GRCh37.p13 chr17: 28,396,315-28,873,715 SLC6A4, LOC105371720, 13 more genes
    nsv7058412inversion1nstd229human GRCh38 chr17: 30,021,943-32,643,975 , GRCh37.p13 chr17: 28,348,961-30,970,993 RNU6-990P, LOC105371730, 81 more genes
    nsv6996196copy number variation1nstd229human GRCh38 chr17: 30,081,593-30,087,636 , GRCh37.p13 chr17: 28,408,611-28,414,654 EFCAB5
    nsv6994136copy number variation1nstd229human GRCh38 chr17: 29,932,266-29,952,228 , GRCh37.p13 chr17: 28,259,284-28,279,246 EFCAB5
    nsv6992581copy number variation1nstd229human GRCh38 chr17: 30,018,945-30,026,727 , GRCh37.p13 chr17: 28,345,963-28,353,745 EFCAB5
    nsv6992328copy number variation1nstd229human GRCh38 chr17: 29,955,243-29,964,233 , GRCh37.p13 chr17: 28,282,261-28,291,251 EFCAB5
    nsv6992024copy number variation1nstd229human GRCh38 chr17: 30,008,268-30,012,437 , GRCh37.p13 chr17: 28,335,286-28,339,455 EFCAB5
    nsv6991728copy number variation1nstd229human GRCh38 chr17: 30,092,677-30,097,344 , GRCh37.p13 chr17: 28,419,695-28,424,362 EFCAB5
    nsv6991526copy number variation1nstd229human GRCh38 chr17: 30,018,001-30,026,400 , GRCh37.p13 chr17: 28,345,019-28,353,418 EFCAB5
    nsv6990735copy number variation1nstd229human GRCh38 chr17: 30,092,049-30,095,091 , GRCh37.p13 chr17: 28,419,067-28,422,109 EFCAB5
    nsv6990530copy number variation1nstd229human GRCh38 chr17: 29,959,405-29,967,721 , GRCh37.p13 chr17: 28,286,423-28,294,739 EFCAB5
    nsv6987789copy number variation1nstd229human GRCh38 chr17: 29,928,490-29,940,940 , GRCh37.p13 chr17: 28,255,508-28,267,958 SSH2, EFCAB5
    nsv6987664copy number variation1nstd229human GRCh38 chr17: 29,934,838-29,943,528 , GRCh37.p13 chr17: 28,261,856-28,270,546 EFCAB5
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