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Items: 1 to 20 of 166

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097853copy number variation1nstd102humanPathogenic GRCh37 chr7: 104,456,677-108,155,935 , GRCh38.p12 chr7: 104,816,230-108,515,491 RNU6-1322P, COG5, 57 more genes
    nsv7097099copy number variation1nstd102humanUncertain significance GRCh37 chr7: 102,937,907-107,643,330 , GRCh38.p12 chr7: 103,297,460-108,002,885 SRPK2, SYPL1, 60 more genes
    nsv6827392copy number variation1nstd229human GRCh38 chr7: 106,892,697-106,896,487 , GRCh37.p13 chr7: 106,533,142-106,536,932 PIK3CG
    nsv6819748copy number variation1nstd229human GRCh38 chr7: 106,905,656-106,911,631 , GRCh37.p13 chr7: 106,546,101-106,552,076 PIK3CG
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6610675copy number variation1nstd223human GRCh38 chr7: 106,902,601-106,903,600 , GRCh37.p13 chr7: 106,543,046-106,544,045 PIK3CG
    nsv6601133copy number variation1nstd223human GRCh38 chr7: 106,905,656-106,911,626 , GRCh37.p13 chr7: 106,546,101-106,552,071 PIK3CG
    nsv6560560inversion1nstd223human GRCh38 chr7: 106,875,074-106,876,162 , GRCh37.p13 chr7: 106,515,519-106,516,607 PIK3CG
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313576copy number variation1nstd102humanPathogenic GRCh37 chr7: 100,676,872-119,156,160 , GRCh38.p12 chr7: 101,033,591-119,516,106 LHFPL3-AS2, CTB-30L5.1, 233 more genes
    nsv6313503copy number variation1nstd102humanPathogenic GRCh37 chr7: 99,417,471-111,586,308 , GRCh38.p12 chr7: 99,819,848-111,946,253 GJC3, LAMB4, 237 more genes
    nsv6136533copy number variation1nstd213human GRCh37 chr7: 104,130,000-120,060,001 , GRCh38.p12 chr7: 104,489,552-120,419,947 CAPZA2, CFTR, 162 more genes
    nsv6135948copy number variation1nstd213human GRCh37 chr7: 105,420,000-108,740,001 , GRCh38.p12 chr7: 105,779,554-109,099,944 NAMPT, COG5, 49 more genes
    nsv6135869copy number variation1nstd213human GRCh37 chr7: 106,370,000-107,370,001 , GRCh38.p12 chr7: 106,729,554-107,729,556 BCAP29, BANF1P5, 14 more genes
    nsv6068032insertion1nstd212human GRCh38 chr7: 106,907,764-106,907,764 , GRCh37.p13 chr7: 106,548,209-106,548,209 PIK3CG
    nsv5723088mobile element insertion1nstd211human GRCh38 chr7: 106,879,142-106,879,142 , GRCh37.p13 chr7: 106,519,587-106,519,587 PIK3CG
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5490714copy number variation1nstd206human GRCh38 chr7: 106,876,129-106,876,182 , GRCh37.p13 chr7: 106,516,574-106,516,627 PIK3CG
    nsv5326600inversion1nstd204human GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904 , ARF5, 752 more genes
    nsv5188569mobile element insertion1nstd203human GRCh38 chr7: 106,900,864-106,900,878 , GRCh37.p13 chr7: 106,541,309-106,541,323 PIK3CG
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