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Items: 1 to 20 of 171

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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
    nsv6776037copy number variation1nstd229human GRCh38 chr5: 115,259,401-115,268,900 , GRCh37.p13 chr5: 114,595,098-114,604,597 PGGT1B, CCDC112, 1 more genes
    nsv6765068copy number variation1nstd229human GRCh38 chr5: 115,294,786-115,294,858 , GRCh37.p13 chr5: 114,630,483-114,630,555 CCDC112
    nsv6759719copy number variation1nstd229human GRCh38 chr5: 115,286,001-115,293,200 , GRCh37.p13 chr5: 114,621,698-114,628,897 CCDC112, HMGN1P15
    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
    nsv6630275copy number variation1nstd224human GRCh37 chr5: 114,593,335-114,611,151 , GRCh38.p12 chr5: 115,257,638-115,275,454 RPS2P26, PGGT1B, 1 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
    nsv6408091copy number variation1nstd223human GRCh38 chr5: 115,281,801-115,283,200 , GRCh37.p13 chr5: 114,617,498-114,618,897 CCDC112
    nsv6401642copy number variation1nstd223human GRCh38 chr5: 115,276,001-115,277,000 , GRCh37.p13 chr5: 114,611,698-114,612,697 CCDC112
    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
    nsv6313580copy number variation1nstd102humanPathogenic GRCh37 chr5: 93,650,000-114,969,108 , GRCh38.p12 chr5: 94,314,295-115,633,411 FER, HMGN1P15, 222 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
    nsv5972434inversion1nstd209human GRCh37.p13 chr5: 114,252,584-114,781,685 , GRCh38 chr5: 114,916,887-115,445,988 CTNNA1P1, PGGT1B, 7 more genes
    nsv5678933mobile element insertion2nstd211human GRCh38 chr5: 115,292,372-115,292,372 , GRCh37.p13 chr5: 114,628,069-114,628,069 CCDC112
    nsv5465334copy number variation1nstd206human GRCh38 chr5: 115,294,786-115,294,861 , GRCh37.p13 chr5: 114,630,483-114,630,558 CCDC112
    nsv5368840translocation1nstd200human GRCh38 chr5: 115,293,205-115,293,205 , GRCh38 chr5: 115,292,271-115,292,271 , GRCh37.p13 chr5: 114,628,902-114,628,902 , GRCh37.p13 chr5: 114,627,968-114,627,968 CCDC112
    nsv5330133translocation1nstd200human GRCh37 chr5: 114,627,968-114,627,968 , GRCh37 chr5: 114,628,902-114,628,902 , GRCh38.p12 chr5: 115,293,205-115,293,205 , GRCh38.p12 chr5: 115,292,271-115,292,271 CCDC112
    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
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