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Items: 1 to 20 of 156

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7054819inversion1nstd229human GRCh38 chr5: 112,393,108-116,183,657 , GRCh37.p13 chr5: 111,728,805-115,519,354 SRP19, LINCADL, 53 more genes
    nsv7053776inversion1nstd229human GRCh38 chr5: 115,805,593-116,116,811 , GRCh37.p13 chr5: 115,141,290-115,452,508 CDO1, ATG12, 7 more genes
    nsv7049327inversion1nstd229human GRCh38 chr5: 115,595,517-116,496,585 , GRCh37.p13 chr5: 114,931,214-115,832,281 MIR12130, COMMD10, 20 more genes
    nsv6776222copy number variation1nstd229human GRCh38 chr5: 115,829,052-115,831,414 , GRCh37.p13 chr5: 115,164,749-115,167,111 ATG12
    nsv6771147copy number variation1nstd229human GRCh38 chr5: 115,761,460-115,934,934 , GRCh37.p13 chr5: 115,097,157-115,270,631 AP3S1, CDO1, 3 more genes
    nsv6637111copy number variation1nstd102humanPathogenic GRCh37 chr5: 112,557,391-128,106,299 , GRCh38.p12 chr5: 113,221,694-128,770,606 SLC12A2, CCDC192, 180 more genes
    nsv6630082copy number variation1nstd224human GRCh37 chr5: 114,279,914-116,657,759 , GRCh38.p12 chr5: 114,944,217-117,322,063 LVRN, TICAM2, 44 more genes
    nsv6408667copy number variation1nstd223human GRCh38 chr5: 115,804,001-115,857,500 , GRCh37.p13 chr5: 115,139,698-115,193,197 AP3S1, ATG12, 1 more genes
    nsv6400401copy number variation1nstd223human GRCh38 chr5: 115,835,301-115,846,400 , GRCh37.p13 chr5: 115,170,998-115,182,097 ATG12, AP3S1
    nsv6313698copy number variation1nstd102humanPathogenic GRCh37 chr5: 111,443,783-116,255,660 , GRCh38.p12 chr5: 112,108,086-116,919,964 RPS17P2, COMMD10, 71 more genes
    nsv6135641copy number variation1nstd213human GRCh37 chr5: 115,060,000-116,040,001 , GRCh38.p12 chr5: 115,724,303-116,704,305 ATG12, SEMA6A, 17 more genes
    nsv6135639copy number variation1nstd213human GRCh37 chr5: 113,920,000-120,810,001 , GRCh38.p12 chr5: 114,584,303-121,474,306 CDO1, AP3S1, 83 more genes
    nsv6135205copy number variation1nstd213human GRCh37 chr5: 91,690,000-180,740,001 , GRCh38.p12 chr5: 92,354,293-181,313,000 ADRA1B, ASS1P10, 1378 more genes
    nsv5715683mobile element insertion1nstd211human GRCh38 chr5: 115,830,140-115,830,140 , GRCh37.p13 chr5: 115,165,837-115,165,837 ATG12
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv5034346inversion1nstd200human GRCh38 chr5: 99,223,339-135,778,784 , GRCh37.p13 chr5: 98,559,043-135,114,473 , NUDT12, 438 more genes
    nsv4947215copy number variation1nstd200human GRCh38 chr5: 93,957,557-155,223,076 , GRCh37.p13 chr5: 93,293,262-154,602,636 , TGFBI, 937 more genes
    nsv4944947copy number variation1nstd200human GRCh38 chr5: 115,831,936-115,832,092 , GRCh37.p13 chr5: 115,167,633-115,167,789 ATG12
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4872282inversion1nstd200human GRCh37 chr5: 98,106,197-132,803,784 , GRCh38.p12 chr5: 98,770,493-133,468,092 , LEAP2, 395 more genes
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