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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097592copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 79,688,289-79,728,896 , GRCh38.p12 chr6: 78,978,572-79,019,179 PHIP, IRAK1BP1
    nsv7097456copy number variation1nstd102humanUncertain significance GRCh37 chr6: 79,787,552-79,787,785 , GRCh38.p12 chr6: 79,077,835-79,078,068 PHIP
    nsv7097093copy number variation2nstd102humanPathogenic GRCh37 chr6: 79,650,410-80,912,949 , GRCh38.p12 chr6: 78,940,693-80,203,232 LOC107986614, LOC643562, 22 more genes
    nsv7054859inversion1nstd229human GRCh38 chr6: 78,924,246-79,955,220 , GRCh37.p13 chr6: 79,633,963-80,664,937 PHIP, HMGN3, 17 more genes
    nsv7054313inversion1nstd229human GRCh38 chr6: 79,007,593-79,007,635 , GRCh37.p13 chr6: 79,717,310-79,717,352 PHIP
    nsv6795102copy number variation1nstd229human GRCh38 chr6: 78,948,225-78,950,079 , GRCh37.p13 chr6: 79,657,942-79,659,796 IRAK1BP1, PHIP
    nsv6794427copy number variation1nstd229human GRCh38 chr6: 79,070,063-79,071,195 , GRCh37.p13 chr6: 79,779,780-79,780,912 PHIP
    nsv6793311copy number variation1nstd229human GRCh38 chr6: 79,045,601-79,049,900 , GRCh37.p13 chr6: 79,755,318-79,759,617 PHIP
    nsv6792673copy number variation1nstd229human GRCh38 chr6: 78,977,843-78,978,463 , GRCh37.p13 chr6: 79,687,560-79,688,180 IRAK1BP1, PHIP
    nsv6791355copy number variation1nstd229human GRCh38 chr6: 78,644,070-79,657,413 , GRCh37.p13 chr6: 79,353,787-80,367,130 HMGN3-AS1, LOC105377867, 13 more genes
    nsv6791212copy number variation1nstd229human GRCh38 chr6: 77,944,413-86,852,671 , GRCh37.p13 chr6: 78,654,130-87,562,389 SH3BGRL2, LCAL1, 93 more genes
    nsv6788868copy number variation1nstd229human GRCh38 chr6: 78,957,910-78,958,391 , GRCh37.p13 chr6: 79,667,627-79,668,108 IRAK1BP1, TRF-GAA8-1, 1 more genes
    nsv6782357copy number variation1nstd229human GRCh38 chr6: 78,901,601-79,108,300 , GRCh37.p13 chr6: 79,611,318-79,818,017 IRAK1BP1, TRF-GAA8-1, 2 more genes
    nsv6781448copy number variation1nstd229human GRCh38 chr6: 79,043,706-79,043,733 , GRCh37.p13 chr6: 79,753,423-79,753,450 PHIP
    nsv6780312copy number variation1nstd229human GRCh38 chr6: 78,978,486-78,980,425 , GRCh37.p13 chr6: 79,688,203-79,690,142 PHIP, IRAK1BP1
    nsv6636747copy number variation1nstd102humanUncertain significance GRCh37 chr6: 77,773,778-80,880,138 , GRCh38.p12 chr6: 77,064,061-80,170,421 TRF-GAA8-1, HMGN3-AS1, 31 more genes
    nsv6634392copy number variation1nstd102humanUncertain significance GRCh37 chr6: 78,911,022-98,909,173 , GRCh38.p12 chr6: 78,201,305-98,461,297 MTHFD2P2, RPL7P27, 212 more genes
    nsv6631542copy number variation1nstd224human GRCh37 chr6: 79,233,635-79,708,000 , GRCh38.p12 chr6: 78,523,918-78,998,283 PHIP, IRAK1BP1, 3 more genes
    nsv6631331copy number variation1nstd224human GRCh37 chr6: 79,241,525-79,708,000 , GRCh38.p12 chr6: 78,531,808-78,998,283 PHIP, IRAK1BP1, 3 more genes
    nsv6631330copy number variation1nstd224human GRCh37 chr6: 79,231,334-79,737,806 , GRCh38.p12 chr6: 78,521,617-79,028,089 TRF-GAA8-1, IRAK1BP1, 3 more genes
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