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Items: 1 to 20 of 111

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148088copy number variation1nstd102humanUncertain significance GRCh37 chr17: 25,263,507-27,829,791 , GRCh38.p12 chr17: 26,936,481-29,502,773 RNU4-34P, RNU6-711P, 95 more genes
    nsv7074961inversion1nstd229human GRCh38 chr17: 27,844,654-28,046,896 , GRCh37.p13 chr17: 26,171,680-26,373,922 LYRM9, LOC102724517, 3 more genes
    nsv7065837inversion1nstd229human GRCh38 chr17: 27,878,514-27,878,558 , GRCh37.p13 chr17: 26,205,540-26,205,584 LYRM9
    nsv7062182inversion1nstd229human GRCh38 chr17: 27,487,612-31,414,648 , GRCh37.p13 chr17: 25,814,638-29,741,666 ERAL1, SARM1, 140 more genes
    nsv6994311copy number variation1nstd229human GRCh38 chr17: 27,868,958-27,882,458 , GRCh37.p13 chr17: 26,195,984-26,209,484 LYRM9
    nsv6989262copy number variation1nstd229human GRCh38 chr17: 27,707,909-27,908,716 , GRCh37.p13 chr17: 26,034,935-26,235,742 LYRM9, LGALS9DP, 1 more genes
    nsv6980392copy number variation1nstd229human GRCh38 chr17: 27,875,901-27,886,500 , GRCh37.p13 chr17: 26,202,927-26,213,526 LYRM9
    nsv6501028copy number variation1nstd223human GRCh38 chr17: 27,881,264-27,883,837 , GRCh37.p13 chr17: 26,208,290-26,210,863 LYRM9
    nsv6314042copy number variation1nstd102humanPathogenic GRCh37 chr17: 21,690,653-28,281,232 , GRCh38.p12 chr17: 22,164,047-29,954,214 TAOK1, TNFAIP1, 131 more genes
    nsv6291821copy number variation1nstd102humanUncertain significance GRCh37 chr17: 25,439,781-26,267,997 , GRCh38.p12 chr17: 27,112,755-27,940,971 ITM2BP1, CPDP1, 17 more genes
    nsv6291525copy number variation1nstd102humanUncertain significance GRCh37 chr17: 25,761,228-26,385,329 , GRCh38.p12 chr17: 27,434,202-28,058,303 LOC102724517, MSANTD3P1, 12 more genes
    nsv6133231copy number variation1nstd213human GRCh37 chr17: 25,820,000-26,720,001 , GRCh38.p12 chr17: 27,492,974-28,392,982 LGALS9, NOS2, 30 more genes
    nsv6133229copy number variation1nstd213human GRCh37 chr17: 25,300,000-32,120,001 , GRCh38.p12 chr17: 26,972,974-33,792,982 BLMH, CPD, 197 more genes
    nsv6133228copy number variation1nstd213human GRCh37 chr17: 25,300,000-27,290,001 , GRCh38.p12 chr17: 26,972,974-28,962,983 LGALS9, RPL23A, 82 more genes
    nsv6095930insertion1nstd212human GRCh38 chr17: 27,887,133-27,887,133 , GRCh37.p13 chr17: 26,214,159-26,214,159 LYRM9
    nsv5550046insertion1nstd206human GRCh38 chr17: 27,887,133-27,887,133 , GRCh37.p13 chr17: 26,214,159-26,214,159 LYRM9
    nsv5377788translocation1nstd200human GRCh38 chr4: 179,342,521-179,342,521 , GRCh38 chr17: 27,887,133-27,887,133 , GRCh37.p13 chr17: 26,214,159-26,214,159 , GRCh37.p13 chr4: 180,263,675-180,263,675 LYRM9
    nsv5334748translocation1nstd200human GRCh37 chr17: 26,214,160-26,214,160 , GRCh37 chr4: 180,263,044-180,263,044 , GRCh38.p12 chr4: 179,341,890-179,341,890 , GRCh38.p12 chr17: 27,887,134-27,887,134 LYRM9
    nsv5333662translocation1nstd200human GRCh37 chr17: 26,214,159-26,214,159 , GRCh37 chr4: 180,263,676-180,263,676 , GRCh38.p12 chr4: 179,342,522-179,342,522 , GRCh38.p12 chr17: 27,887,133-27,887,133 LYRM9
    nsv5141727mobile element insertion1nstd203human GRCh38 chr17: 27,888,687-27,888,700 , GRCh37.p13 chr17: 26,215,713-26,215,726 LYRM9
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