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Items: 1 to 20 of 172

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097560copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr6: 107,019,871-110,266,416 , GRCh38.p12 chr6: 106,571,996-109,945,213 ZPR1P1, OSTM1, 60 more genes
    nsv7050372inversion1nstd229human GRCh38 chr6: 107,280,655-111,259,922 , GRCh37.p13 chr6: 107,601,859-111,581,125 SNORA40C, PPIL6, 77 more genes
    nsv7044587inversion1nstd229human GRCh38 chr6: 107,042,208-108,316,831 , GRCh37.p13 chr6: 107,495,575-108,638,035 RPL3P7, MTHFD2P3, 19 more genes
    nsv7043260inversion1nstd229human GRCh38 chr6: 107,500,793-111,264,842 , GRCh37.p13 chr6: 107,821,997-111,586,045 ZBTB24-DT, RNU6-906P, 76 more genes
    nsv6817729copy number variation1nstd229human GRCh38 chr6: 108,135,696-108,149,176 , GRCh37.p13 chr6: 108,456,900-108,470,380 OSTM1-AS1
    nsv6814658copy number variation1nstd229human GRCh38 chr6: 108,140,678-108,150,505 , GRCh37.p13 chr6: 108,461,882-108,471,709 OSTM1-AS1
    nsv6810483copy number variation1nstd229human GRCh38 chr6: 108,144,373-108,152,302 , GRCh37.p13 chr6: 108,465,577-108,473,506 OSTM1-AS1
    nsv6810126copy number variation1nstd229human GRCh38 chr6: 108,133,892-108,137,943 , GRCh37.p13 chr6: 108,455,096-108,459,147 OSTM1-AS1
    nsv6809159copy number variation1nstd229human GRCh38 chr6: 107,970,989-108,121,645 , GRCh37.p13 chr6: 108,292,193-108,442,849 OSTM1-AS1, LOC105377929, 3 more genes
    nsv6804847copy number variation1nstd229human GRCh38 chr6: 105,481,597-109,225,980 , GRCh37.p13 chr6: 105,929,472-109,547,183 LINC02836, SOBP, 61 more genes
    nsv6802730copy number variation1nstd229human GRCh38 chr6: 108,153,687-108,158,768 , GRCh37.p13 chr6: 108,474,891-108,479,972 OSTM1-AS1
    nsv6637047copy number variation1nstd102humanUncertain significance GRCh37 chr6: 108,189,941-108,498,389 , GRCh38.p12 chr6: 107,868,737-108,177,185 RNU6-437P, RPL3P7, 7 more genes
    nsv6636921copy number variation1nstd102humanUncertain significance GRCh37 chr6: 108,195,840-108,498,389 , GRCh38.p12 chr6: 107,874,636-108,177,185 MTHFD2P3, RPL3P7, 7 more genes
    nsv6618866copy number variation1nstd223human GRCh38 chr6: 108,133,892-108,137,941 , GRCh37.p13 chr6: 108,455,096-108,459,145 OSTM1-AS1
    nsv6604596copy number variation1nstd223human GRCh38 chr6: 108,152,701-108,183,000 , GRCh37.p13 chr6: 108,473,905-108,504,204 NR2E1, OSTM1-AS1
    nsv6603806copy number variation1nstd223human GRCh38 chr6: 108,154,101-108,159,100 , GRCh37.p13 chr6: 108,475,305-108,480,304 OSTM1-AS1
    nsv6571485inversion1nstd223human GRCh38 chr6: 108,151,613-108,152,241 , GRCh37.p13 chr6: 108,472,817-108,473,445 OSTM1-AS1
    nsv6555943inversion1nstd223human GRCh38 chr6: 108,144,469-108,144,940 , GRCh37.p13 chr6: 108,465,673-108,466,144 OSTM1-AS1
    nsv6313858copy number variation1nstd102humanPathogenic GRCh37 chr6: 92,054,891-118,329,651 , GRCh38.p12 chr6: 91,345,173-118,008,488 RN7SL509P, LAMA4, 311 more genes
    nsv6257007mobile element insertion1nstd215human GRCh38 chr6: 108,151,463-108,151,463 , GRCh37.p13 chr6: 108,472,667-108,472,667 OSTM1-AS1
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