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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7139118copy number variation1nstd232human GRCh37.p13 chr2: 109,092,089-109,092,204 , GRCh38.p12 chr2: 108,475,633-108,475,748 GCC2
    nsv7095847copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr2: 108,604,612-109,579,739 , GRCh38.p12 chr2: 107,988,156-108,963,283 ACTP1, GCC2-AS1, 21 more genes
    nsv7046376inversion1nstd229human GRCh38 chr2: 106,214,512-108,776,331 , GRCh37.p13 chr2: 106,830,968-109,392,787 LOC107985931, LOC107985802, 42 more genes
    nsv7044675inversion1nstd229human GRCh38 chr2: 106,399,909-108,512,921 , GRCh37.p13 chr2: 107,016,365-109,129,377 GMCL1P2, SULT1C2, 30 more genes
    nsv7038094inversion1nstd229human GRCh38 chr2: 106,480,616-110,213,336 , GRCh37.p13 chr2: 107,097,072-110,970,913 WASF1P1, LOC105373985, 72 more genes
    nsv6694285copy number variation1nstd229human GRCh38 chr2: 108,477,812-108,512,128 , GRCh37.p13 chr2: 109,094,268-109,128,584 GCC2-AS1, GCC2
    nsv6689266copy number variation1nstd229human GRCh38 chr2: 108,420,201-108,560,000 , GRCh37.p13 chr2: 109,036,657-109,176,456 LIMS1, GCC2, 2 more genes
    nsv6688554copy number variation1nstd229human GRCh38 chr2: 108,474,319-108,485,472 , GRCh37.p13 chr2: 109,090,775-109,101,928 GCC2
    nsv6686545copy number variation1nstd229human GRCh38 chr2: 103,585,907-110,943,040 , GRCh37.p13 chr2: 104,202,365-111,700,617 PPP1R2P5, CAPZBP1, 142 more genes
    nsv6683844copy number variation1nstd229human GRCh38 chr2: 108,465,554-108,521,567 , GRCh37.p13 chr2: 109,082,010-109,138,023 GCC2-AS1, GCC2
    nsv6678300copy number variation1nstd229human GRCh38 chr2: 108,504,659-108,505,016 , GRCh37.p13 chr2: 109,121,115-109,121,472 GCC2
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CYP1B1-AS1, LOC107985771, 1649 more genes
    nsv6546843inversion1nstd223human GRCh38 chr2: 108,453,734-108,453,998 , GRCh37.p13 chr2: 109,070,190-109,070,454 GCC2
    nsv6541943inversion1nstd223human GRCh38 chr2: 108,336,670-109,113,885 , GRCh37.p13 chr2: 108,953,126-109,730,341 EDAR, GCC2-AS1, 12 more genes
    nsv6540094inversion1nstd223human GRCh38 chr2: 108,488,109-108,489,410 , GRCh37.p13 chr2: 109,104,565-109,105,866 GCC2
    nsv6355233copy number variation1nstd223human GRCh38 chr2: 108,459,934-108,461,643 , GRCh37.p13 chr2: 109,076,390-109,078,099 GCC2
    nsv6352531copy number variation1nstd223human GRCh38 chr2: 108,493,023-108,493,700 , GRCh37.p13 chr2: 109,109,479-109,110,156 GCC2
    nsv6348044copy number variation1nstd223human GRCh38 chr2: 107,883,785-108,500,628 , GRCh37.p13 chr2: 108,500,241-109,117,084 ACTP1, SLC5A7, 15 more genes
    nsv6347189copy number variation1nstd223human GRCh38 chr2: 108,476,566-108,478,417 , GRCh37.p13 chr2: 109,093,022-109,094,873 GCC2
    nsv6315410copy number variation1nstd102humanUncertain significance GRCh37 chr2: 108,446,955-110,504,318 , GRCh38.p12 chr2: 107,830,499-109,746,741 SULT1C3, SH3RF3-AS1, 37 more genes
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