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Items: 1 to 20 of 297

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098118copy number variation1nstd102humanUncertain significance GRCh37 chr7: 37,934,048-37,936,694 , GRCh38.p12 chr7: 37,894,446-37,897,092 NME8
    nsv7054398inversion1nstd229human GRCh38 chr7: 37,866,117-37,866,235 , GRCh37.p13 chr7: 37,905,719-37,905,837 NME8
    nsv6837340copy number variation1nstd229human GRCh38 chr7: 37,891,470-37,897,129 , GRCh37.p13 chr7: 37,931,072-37,936,731 NME8
    nsv6834321copy number variation1nstd229human GRCh38 chr7: 37,859,139-37,859,222 , GRCh37.p13 chr7: 37,898,741-37,898,824 NME8
    nsv6833957copy number variation1nstd229human GRCh38 chr7: 37,840,989-37,859,372 , GRCh37.p13 chr7: 37,880,591-37,898,974 NME8
    nsv6832607copy number variation1nstd229human GRCh38 chr7: 37,899,413-37,902,137 , GRCh37.p13 chr7: 37,939,015-37,941,739 NME8
    nsv6830516copy number variation1nstd229human GRCh38 chr7: 37,730,544-37,851,463 , GRCh37.p13 chr7: 37,770,146-37,891,065 NME8, GPR141BP, 1 more genes
    nsv6824674copy number variation1nstd229human GRCh38 chr7: 37,895,995-37,905,859 , GRCh37.p13 chr7: 37,935,597-37,945,461 NME8, SFRP4
    nsv6822451copy number variation1nstd229human GRCh38 chr7: 37,779,518-37,947,724 , GRCh37.p13 chr7: 37,819,120-37,987,326 SFRP4, GPR141BP, 2 more genes
    nsv6821026copy number variation1nstd229human GRCh38 chr7: 37,895,300-37,925,037 , GRCh37.p13 chr7: 37,934,902-37,964,639 SFRP4, EPDR1, 1 more genes
    nsv6636700copy number variation1nstd102humanUncertain significance GRCh37 chr7: 36,374,178-37,923,116 , GRCh38.p12 chr7: 36,334,569-37,883,514 GPR141, AOAH, 14 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6619956copy number variation1nstd223human GRCh38 chr7: 37,890,112-37,890,751 , GRCh37.p13 chr7: 37,929,714-37,930,353 NME8
    nsv6614342copy number variation1nstd223human GRCh38 chr7: 37,730,544-37,851,461 , GRCh37.p13 chr7: 37,770,146-37,891,063 GPR141, NME8, 1 more genes
    nsv6610460copy number variation1nstd223human GRCh38 chr7: 37,890,401-37,897,300 , GRCh37.p13 chr7: 37,930,003-37,936,902 NME8
    nsv6609617copy number variation1nstd223human GRCh38 chr7: 37,888,401-37,890,300 , GRCh37.p13 chr7: 37,928,003-37,929,902 NME8
    nsv6608386copy number variation1nstd223human GRCh38 chr7: 37,891,301-37,895,300 , GRCh37.p13 chr7: 37,930,903-37,934,902 NME8
    nsv6608152copy number variation1nstd223human GRCh38 chr7: 37,898,020-37,898,421 , GRCh37.p13 chr7: 37,937,622-37,938,023 NME8
    nsv6607404copy number variation1nstd223human GRCh38 chr7: 37,853,048-37,853,114 , GRCh37.p13 chr7: 37,892,650-37,892,716 NME8
    nsv6606114copy number variation1nstd223human GRCh38 chr7: 37,891,018-37,891,515 , GRCh37.p13 chr7: 37,930,620-37,931,117 NME8
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