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Items: 1 to 20 of 473

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137045copy number variation1nstd102humanPathogenic GRCh37 chr1: 536,777-6,012,896 , GRCh38.p12 chr1: 601,397-5,952,836 MIR200B, LOC105378608, 172 more genes
    nsv7099170copy number variation1nstd231human GRCh38.p12 chr1: 1,558,660-2,125,257 , GRCh37 chr1: 1,494,040-2,056,696 CDK11B, GABRD, 23 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
    nsv7044661inversion1nstd229human GRCh38 chr1: 1,842,037-1,948,127 , GRCh37.p13 chr1: 1,773,476-1,879,566 GNB1, CALML6, 3 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
    nsv7041794inversion1nstd229human GRCh38 chr1: 1,706,341-1,930,482 , GRCh37.p13 chr1: 1,637,780-1,861,921 SLC35E2A, CDK11A, 8 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
    nsv6646788copy number variation1nstd229human GRCh38 chr1: 1,916,826-1,919,242 , GRCh37.p13 chr1: 1,848,265-1,850,681 TMEM52, CALML6
    nsv6646784copy number variation1nstd229human GRCh38 chr1: 1,910,717-1,918,022 , GRCh37.p13 chr1: 1,842,156-1,849,461 TMEM52, CALML6
    nsv6646592copy number variation1nstd229human GRCh38 chr1: 1,878,328-2,037,158 , GRCh37.p13 chr1: 1,809,767-1,968,597 GABRD, CALML6, 7 more genes
    nsv6646485copy number variation1nstd229human GRCh38 chr1: 1,875,866-1,950,875 , GRCh37.p13 chr1: 1,807,305-1,882,314 GNB1-DT, CFAP74, 3 more genes
    nsv6645994copy number variation1nstd229human GRCh38 chr1: 1,834,972-2,057,979 , GRCh37.p13 chr1: 1,766,411-1,989,418 LOC105378589, CALML6, 9 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
    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
    nsv6636682copy number variation1nstd102humanUncertain significance GRCh37 chr1: 1,732,310-2,040,647 , GRCh38.p12 chr1: 1,800,871-2,109,208 LOC105378590, TMEM52, 9 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
    nsv6636496copy number variation1nstd102humanUncertain significance GRCh37 chr1: 1,751,300-2,107,605 , GRCh38.p12 chr1: 1,819,861-2,176,166 LOC105378589, LOC107984872, 9 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
    nsv6626057copy number variation1nstd224human GRCh37 chr1: 1,804,302-2,040,936 , GRCh38.p12 chr1: 1,872,863-2,109,497 GABRD, TMEM52, 9 more genes
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