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Items: 1 to 20 of 176

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097565copy number variation1nstd102humanUncertain significance GRCh37 chr6: 109,773,694-109,775,462 , GRCh38.p12 chr6: 109,452,491-109,454,259 MICAL1
    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
    nsv7097173copy number variation1nstd102humanUncertain significance GRCh37 chr6: 109,765,394-110,064,995 , GRCh38.p12 chr6: 109,444,191-109,743,792 ZBTB24, AK9, 4 more genes
    nsv7097034copy number variation1nstd102humanUncertain significance GRCh37 chr6: 109,766,954-109,767,085 , GRCh38.p12 chr6: 109,445,751-109,445,882 MICAL1
    nsv7097033copy number variation1nstd102humanUncertain significance GRCh37 chr6: 109,690,054-110,266,416 , GRCh38.p12 chr6: 109,368,851-109,945,213 MICAL1, ZBTB24, 6 more genes
    nsv7055005inversion1nstd229human GRCh38 chr6: 108,167,886-110,172,775 , GRCh37.p13 chr6: 108,489,090-110,493,978 AK9, WASF1, 34 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
    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
    nsv6812335copy number variation1nstd229human GRCh38 chr6: 109,457,456-109,459,218 , GRCh37.p13 chr6: 109,778,659-109,780,421 MICAL1
    nsv6811557copy number variation1nstd229human GRCh38 chr6: 109,387,099-109,733,012 , GRCh37.p13 chr6: 109,708,302-110,054,215 ZBTB24, FIG4, 5 more genes
    nsv6810879copy number variation1nstd229human GRCh38 chr6: 109,404,650-109,758,419 , GRCh37.p13 chr6: 109,725,853-110,079,622 SMPD2, ZBTB24-DT, 5 more genes
    nsv6809521copy number variation1nstd229human GRCh38 chr6: 109,452,476-109,455,102 , GRCh37.p13 chr6: 109,773,679-109,776,305 MICAL1
    nsv6809456copy number variation1nstd229human GRCh38 chr6: 109,380,401-109,512,000 , GRCh37.p13 chr6: 109,701,604-109,833,203 PPIL6, AK9, 5 more genes
    nsv6804560copy number variation1nstd229human GRCh38 chr6: 109,439,129-109,712,400 , GRCh37.p13 chr6: 109,760,332-110,033,603 AK9, ZBTB24, 5 more genes
    nsv6800686copy number variation1nstd229human GRCh38 chr6: 109,455,273-109,455,327 , GRCh37.p13 chr6: 109,776,476-109,776,530 MICAL1
    nsv6799509copy number variation1nstd229human GRCh38 chr6: 109,282,211-109,485,074 , GRCh37.p13 chr6: 109,603,414-109,806,277 ZBTB24-DT, SMPD2, 8 more genes
    nsv6798389copy number variation1nstd229human GRCh38 chr6: 109,382,001-109,511,500 , GRCh37.p13 chr6: 109,703,204-109,832,703 PPIL6, AK9, 5 more genes
    nsv6637155copy number variation1nstd102humanUncertain significance GRCh37 chr6: 109,576,603-109,878,834 , GRCh38.p12 chr6: 109,255,400-109,557,631 RNY3P11, ZBTB24, 9 more genes
    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
    nsv6141016copy number variation1nstd206human GRCh38 chr6: 109,444,790-109,450,790 , GRCh37.p13 chr6: 109,765,993-109,771,993 MICAL1
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