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Items: 1 to 20 of 602

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137191copy number variation1nstd102humanPathogenic GRCh37 chr1: 1,957,148-6,553,454 , GRCh38.p12 chr1: 2,025,709-6,493,394 LOC102724429, TNFRSF14, 86 more genes
    nsv7137045copy number variation1nstd102humanPathogenic GRCh37 chr1: 536,777-6,012,896 , GRCh38.p12 chr1: 601,397-5,952,836 MIR200B, LOC105378608, 172 more genes
    nsv7099018copy number variation1nstd102humanPathogenic GRCh37 chr1: 1-2,580,976 , GRCh38.p12 chr1: 10,001-2,649,537 DVL1, LOC100129534, 148 more genes
    nsv7058041inversion1nstd229human GRCh38 chr1: 1,845,355-9,534,096 , GRCh37.p13 chr1: 1,776,794-9,594,155 RPL37P9, TMEM52, 152 more genes
    nsv7044270inversion1nstd229human GRCh38 chr1: 1,133,718-2,842,494 , GRCh37.p13 chr1: 1,069,098-2,759,059 LOC105378586, MIR6726, 91 more genes
    nsv6647368copy number variation1nstd229human GRCh38 chr1: 2,211,693-2,212,194 , GRCh37.p13 chr1: 2,143,132-2,143,633 FAAP20
    nsv6647358copy number variation1nstd229human GRCh38 chr1: 2,193,358-2,196,994 , GRCh37.p13 chr1: 2,124,797-2,128,433 FAAP20
    nsv6647355copy number variation1nstd229human GRCh38 chr1: 2,185,459-2,190,829 , GRCh37.p13 chr1: 2,116,898-2,122,268 PRKCZ, FAAP20, 1 more genes
    nsv6647125copy number variation1nstd229human GRCh38 chr1: 2,159,969-2,230,688 , GRCh37.p13 chr1: 2,091,408-2,162,127 LOC105378593, PRKCZ-AS1, 4 more genes
    nsv6647095copy number variation1nstd229human GRCh38 chr1: 2,088,922-2,212,456 , GRCh37.p13 chr1: 2,020,361-2,143,895 LOC112268219, PRKCZ-AS1, 3 more genes
    nsv6646981copy number variation1nstd229human GRCh38 chr1: 2,181,779-2,186,830 , GRCh37.p13 chr1: 2,113,218-2,118,269 PRKCZ-AS1, PRKCZ, 1 more genes
    nsv6646938copy number variation1nstd229human GRCh38 chr1: 1,902,798-2,318,810 , GRCh37.p13 chr1: 1,834,237-2,250,249 TMEM52, GABRD, 12 more genes
    nsv6646456copy number variation1nstd229human GRCh38 chr1: 2,007,501-2,204,900 , GRCh37.p13 chr1: 1,938,940-2,136,339 PRKCZ-DT, LOC112268219, 6 more genes
    nsv6637093copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,467-12,448,956 , GRCh38.p12 chr1: 914,087-12,388,897 VWA1, CEP104, 311 more genes
    nsv6637082copy number variation1nstd102humanPathogenic GRCh37 chr1: 2,056,695-2,447,725 , GRCh38.p12 chr1: 2,125,256-2,516,286 PRKCZ, PRKCZ-AS1, 10 more genes
    nsv6636801copy number variation1nstd102humanPathogenic GRCh37 chr1: 1,335,011-2,302,755 , GRCh38.p12 chr1: 1,399,631-2,371,316 SSU72, MRPL20, 44 more genes
    nsv6636661copy number variation1nstd102humanUncertain significance GRCh37 chr1: 1,130,311-2,397,177 , GRCh38.p12 chr1: 1,194,931-2,465,738 ATAD3C, ACAP3, 69 more genes
    nsv6636292copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,467-2,972,435 , GRCh38.p12 chr1: 914,087-3,055,871 LOC105378602, LOC105378599, 108 more genes
    nsv6626162copy number variation7nstd224human GRCh37 chr1: 2,142,496-2,160,488 , GRCh38.p12 chr1: 2,211,057-2,229,049 SKI, FAAP20
    nsv6626161copy number variation1nstd224human GRCh37 chr1: 2,139,916-2,160,552 , GRCh38.p12 chr1: 2,208,477-2,229,113 SKI, FAAP20, 1 more genes
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