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Items: 1 to 20 of 137

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7060408inversion1nstd229human GRCh38 chr17: 32,053,960-32,158,173 , GRCh37.p13 chr17: 30,380,979-30,485,192 RHOT1, ARGFXP2, 4 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
    nsv6992591copy number variation1nstd229human GRCh38 chr17: 32,148,890-32,152,428 , GRCh37.p13 chr17: 30,475,909-30,479,447 ARGFXP2, RHOT1
    nsv6992022copy number variation1nstd229human GRCh38 chr17: 32,151,652-32,154,304 , GRCh37.p13 chr17: 30,478,671-30,481,323 ARGFXP2, RHOT1
    nsv6989364copy number variation1nstd229human GRCh38 chr17: 32,143,583-32,162,078 , GRCh37.p13 chr17: 30,470,602-30,489,097 LOC105371730, RHOT1, 1 more genes
    nsv6986239copy number variation1nstd229human GRCh38 chr17: 31,984,901-32,187,900 , GRCh37.p13 chr17: 30,311,920-30,514,919 LOC102724625, ARGFXP2, 6 more genes
    nsv6983541copy number variation1nstd229human GRCh38 chr17: 32,054,001-32,209,600 , GRCh37.p13 chr17: 30,381,020-30,536,619 RHOT1, ARGFXP2, 3 more genes
    nsv6980451copy number variation1nstd229human GRCh38 chr17: 29,103,792-32,176,512 , GRCh37.p13 chr17: 27,430,810-30,503,531 SMURF2P1-LRRC37BP1, RNU6-990P, 90 more genes
    nsv6513974copy number variation1nstd223human GRCh38 chr17: 32,151,703-32,154,304 , GRCh37.p13 chr17: 30,478,722-30,481,323 RHOT1, ARGFXP2
    nsv6509585copy number variation1nstd223human GRCh38 chr17: 32,148,214-32,154,820 , GRCh37.p13 chr17: 30,475,233-30,481,839 RHOT1, ARGFXP2
    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
    nsv6133048copy number variation1nstd213human GRCh37 chr17: 30,350,000-30,530,001 , GRCh38.p12 chr17: 32,022,981-32,202,982 SH3GL1P1, RHOT1, 5 more genes
    nsv6133047copy number variation1nstd213human GRCh37 chr17: 30,150,000-30,710,001 , GRCh38.p12 chr17: 31,822,981-32,382,982 SH3GL1P1, ZNF207, 16 more genes
    nsv5940381copy number variation1nstd209human GRCh38 chr17: 32,151,614-32,154,330 , GRCh37.p13 chr17: 30,478,633-30,481,349 RHOT1, ARGFXP2
    nsv5561493sequence alteration1nstd206human GRCh37.p13 chr17: 30,380,978-30,536,565 , GRCh38 chr17: 32,053,959-32,209,546 RHOT1, LRRC37B, 4 more genes
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5532625copy number variation1nstd206human GRCh38 chr17: 32,148,559-32,153,464 , GRCh37.p13 chr17: 30,475,578-30,480,483 ARGFXP2, RHOT1
    nsv5328617translocation1nstd204human GRCh37.p13 chr17: 30,480,483-30,480,483 , GRCh37.p13 chr17: 30,475,578-30,475,578 , GRCh38.p13 chr17: 32,153,464-32,153,464 , GRCh38.p13 chr17: 32,148,559-32,148,559 RHOT1, ARGFXP2
    nsv5296147copy number variation1nstd204human GRCh38.p13 chr17: 32,148,223-32,153,365 , GRCh37.p13 chr17: 30,475,242-30,480,384 RHOT1, ARGFXP2
    nsv5016042copy number variation1nstd200human GRCh38 chr17: 32,148,890-32,152,424 , GRCh37.p13 chr17: 30,475,909-30,479,443 RHOT1, ARGFXP2
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