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Items: 1 to 20 of 495

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098991copy number variation1nstd102humanLikely pathogenic GRCh37 chr18: 44,098,220-44,104,428 , GRCh38.p12 chr18: 46,518,257-46,524,465 LOXHD1
    nsv7098772copy number variation1nstd102humanLikely benign GRCh37 chr18: 44,222,000-44,236,997 , GRCh38.p12 chr18: 46,642,037-46,657,034 LOXHD1
    nsv7095444copy number variation1nstd102humanPathogenic GRCh37 chr18: 42,281,312-44,236,996 , GRCh38.p12 chr18: 44,701,347-46,657,033 HAUS1, ARK2C, 21 more genes
    nsv7095381copy number variation1nstd102humanPathogenic GRCh37 chr18: 44,190,729-44,190,897 , GRCh38.p12 chr18: 46,610,766-46,610,934 LOXHD1
    nsv7095380copy number variation1nstd102humanPathogenic GRCh37 chr18: 44,139,401-44,143,198 , GRCh38.p12 chr18: 46,559,438-46,563,235 LOXHD1
    nsv7095011copy number variation1nstd102humanPathogenic GRCh37 chr18: 44,143,018-44,143,198 , GRCh38.p12 chr18: 46,563,055-46,563,235 LOXHD1
    nsv7095010copy number variation1nstd102humanPathogenic GRCh37 chr18: 44,125,270-44,184,202 , GRCh38.p12 chr18: 46,545,307-46,604,239 LOXHD1
    nsv7095009copy number variation1nstd102humanPathogenic GRCh37 chr18: 44,121,729-44,127,031 , GRCh38.p12 chr18: 46,541,766-46,547,068 LOXHD1
    nsv7094935copy number variation1nstd102humanLikely pathogenic GRCh37 chr18: 44,104,661-44,109,304 , GRCh38.p12 chr18: 46,524,698-46,529,341 LOXHD1
    nsv7074210inversion1nstd229human GRCh38 chr18: 45,861,287-52,164,943 , GRCh37.p13 chr18: 43,441,252-49,691,313 LOC105372100, RNA5SP458, 103 more genes
    nsv7065765inversion1nstd229human GRCh38 chr18: 46,426,327-48,440,063 , GRCh37.p13 chr18: 44,006,290-45,966,434 ZBTB7C, MIR4527, 29 more genes
    nsv7062073inversion1nstd229human GRCh38 chr18: 42,140,183-50,368,023 , GRCh37.p13 chr18: 39,720,147-47,894,393 ACAA2, MIR4320, 105 more genes
    nsv7060607inversion1nstd229human GRCh38 chr18: 46,563,922-48,670,215 , GRCh37.p13 chr18: 44,143,885-46,196,586 SKOR2, ELOA3DP, 32 more genes
    nsv7016762copy number variation1nstd229human GRCh38 chr18: 46,604,057-46,628,913 , GRCh37.p13 chr18: 44,184,020-44,208,876 LOXHD1
    nsv7016027copy number variation1nstd229human GRCh38 chr18: 46,570,779-46,571,111 , GRCh37.p13 chr18: 44,150,742-44,151,074 LOXHD1
    nsv7015759copy number variation1nstd229human GRCh38 chr18: 46,490,990-46,500,603 , GRCh37.p13 chr18: 44,070,953-44,080,566 LOXHD1
    nsv7015474copy number variation1nstd229human GRCh38 chr18: 46,521,174-46,527,180 , GRCh37.p13 chr18: 44,101,137-44,107,143 LOXHD1
    nsv7015390copy number variation1nstd229human GRCh38 chr18: 46,550,774-46,556,741 , GRCh37.p13 chr18: 44,130,737-44,136,704 LOXHD1
    nsv7014519copy number variation1nstd229human GRCh38 chr18: 46,642,833-46,683,992 , GRCh37.p13 chr18: 44,222,796-44,263,955 LOC105372096, LOXHD1, 1 more genes
    nsv7013738copy number variation1nstd229human GRCh38 chr18: 46,581,101-46,621,700 , GRCh37.p13 chr18: 44,161,064-44,201,663 LOXHD1
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