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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6696408copy number variation1nstd229human GRCh38 chr2: 183,124,918-183,125,473 , GRCh37.p13 chr2: 183,989,646-183,990,201 NUP35
    nsv6694408copy number variation1nstd229human GRCh38 chr2: 182,991,663-184,070,054 , GRCh37.p13 chr2: 183,856,391-184,934,781 KRT8P10, NCKAP1, 4 more genes
    nsv6691127copy number variation1nstd229human GRCh38 chr2: 182,730,019-183,183,033 , GRCh37.p13 chr2: 183,594,746-184,047,761 DNAJC10, RPL31P15, 6 more genes
    nsv6690951copy number variation1nstd229human GRCh38 chr2: 183,080,601-183,128,900 , GRCh37.p13 chr2: 183,945,329-183,993,628 NUP35, DUSP19
    nsv6685517copy number variation1nstd229human GRCh38 chr2: 183,122,788-183,122,864 , GRCh37.p13 chr2: 183,987,516-183,987,592 NUP35
    nsv6683213copy number variation1nstd229human GRCh38 chr2: 183,127,433-183,127,564 , GRCh37.p13 chr2: 183,992,161-183,992,292 NUP35
    nsv6682779copy number variation1nstd229human GRCh38 chr2: 183,145,901-183,148,900 , GRCh37.p13 chr2: 184,010,629-184,013,628 NUP35
    nsv6682197copy number variation1nstd229human GRCh38 chr2: 183,120,018-183,125,190 , GRCh37.p13 chr2: 183,984,746-183,989,918 NUP35
    nsv6680835copy number variation1nstd229human GRCh38 chr2: 183,121,263-183,134,193 , GRCh37.p13 chr2: 183,985,991-183,998,921 NUP35
    nsv6636434copy number variation1nstd102humanUncertain significance GRCh37 chr2: 183,206,179-184,174,590 , GRCh38.p12 chr2: 182,341,452-183,309,862 DNAJC10, LIN28AP1, 9 more genes
    nsv6636283copy number variation1nstd102humanUncertain significance GRCh37 chr2: 183,070,475-186,717,885 , GRCh38.p12 chr2: 182,205,748-185,853,158 LOC101929976, LOC105373781, 28 more genes
    nsv6635310copy number variation1nstd227human GRCh37 chr2: 183,988,599-184,000,361 , GRCh38.p12 chr2: 183,123,871-183,135,633 NUP35
    nsv6634816copy number variation1nstd227human GRCh37 chr2: 183,988,599-183,991,266 , GRCh38.p12 chr2: 183,123,871-183,126,538 NUP35
    nsv6548079inversion1nstd223human GRCh38 chr2: 178,157,654-187,669,944 , GRCh37.p13 chr2: 179,022,381-188,534,671 RNU7-104P, RN7SKP42, 90 more genes
    nsv6547527inversion1nstd223human GRCh38 chr2: 183,137,640-183,139,309 , GRCh37.p13 chr2: 184,002,368-184,004,037 NUP35
    nsv6540358inversion1nstd223human GRCh38 chr2: 183,146,223-183,146,616 , GRCh37.p13 chr2: 184,010,951-184,011,344 NUP35
    nsv6355450copy number variation1nstd223human GRCh38 chr2: 183,121,263-183,134,192 , GRCh37.p13 chr2: 183,985,991-183,998,920 NUP35
    nsv6352732copy number variation1nstd223human GRCh38 chr2: 183,124,918-183,125,473 , GRCh37.p13 chr2: 183,989,646-183,990,201 NUP35
    nsv6344577copy number variation1nstd223human GRCh38 chr2: 183,114,883-183,116,221 , GRCh37.p13 chr2: 183,979,611-183,980,949 NUP35
    nsv6338683copy number variation1nstd223human GRCh38 chr2: 183,120,263-183,121,614 , GRCh37.p13 chr2: 183,984,991-183,986,342 NUP35
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