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Items: 1 to 20 of 147

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7047569inversion1nstd229human GRCh38 chr3: 152,490,812-161,531,961 , GRCh37.p13 chr3: 152,208,601-161,249,749 RPS2P19, LOC112268450, 128 more genes
    nsv6734412copy number variation1nstd229human GRCh38 chr3: 156,542,634-156,543,569 , GRCh37.p13 chr3: 156,260,423-156,261,358 SSR3, KCNAB1
    nsv6733433copy number variation1nstd229human GRCh38 chr3: 156,550,277-156,570,187 , GRCh37.p13 chr3: 156,268,066-156,287,976 SSR3
    nsv6729324copy number variation1nstd229human GRCh38 chr3: 156,546,348-156,557,278 , GRCh37.p13 chr3: 156,264,137-156,275,067 SSR3
    nsv6724729copy number variation1nstd229human GRCh38 chr3: 156,014,310-156,940,321 , GRCh37.p13 chr3: 155,732,099-156,658,110 ALG1L15P, SSR3, 12 more genes
    nsv6722255copy number variation1nstd229human GRCh38 chr3: 156,538,501-156,541,700 , GRCh37.p13 chr3: 156,256,290-156,259,489 SSR3, KCNAB1
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 H1-10, AADACL2-AS1, 846 more genes
    nsv6372621copy number variation1nstd223human GRCh38 chr3: 156,551,701-156,556,800 , GRCh37.p13 chr3: 156,269,490-156,274,589 SSR3
    nsv6366376copy number variation1nstd223human GRCh38 chr3: 155,746,388-156,594,198 , GRCh37.p13 chr3: 155,464,177-156,311,987 SNRNP40P1, MRE11P1, 12 more genes
    nsv6363259copy number variation1nstd223human GRCh38 chr3: 156,550,277-156,570,184 , GRCh37.p13 chr3: 156,268,066-156,287,973 SSR3
    nsv6313678copy number variation1nstd102humanPathogenic GRCh37 chr3: 145,486,960-160,504,834 , GRCh38.p12 chr3: 145,769,173-160,787,046 RNU6-901P, RPL32P8, 229 more genes
    nsv6290273copy number variation1nstd102humanPathogenic GRCh37 chr3: 142,729,607-157,921,084 , GRCh38.p12 chr3: 143,010,765-158,203,295 LINC02066, TM4SF1-AS1, 206 more genes
    nsv6290244copy number variation1nstd102humanPathogenic GRCh37 chr3: 143,439,359-165,252,122 , GRCh38.p12 chr3: 143,720,517-165,534,334 LOC102724145, C3orf80, 273 more genes
    nsv6134788copy number variation1nstd213human GRCh37 chr3: 155,010,000-169,630,001 , GRCh38.p12 chr3: 155,292,211-169,912,213 , BCHE, 171 more genes
    nsv5689283mobile element insertion1nstd211human GRCh38 chr3: 156,538,266-156,538,266 , GRCh37.p13 chr3: 156,256,055-156,256,055 SSR3, KCNAB1
    nsv5381765copy number variation1nstd102humanPathogenic GRCh37 chr3: 138,173,683-162,494,699 , GRCh38.p12 chr3: 138,454,841-162,776,911 MBNL1-AS1, LOC107986138, 339 more genes
    nsv5352071translocation1nstd200human GRCh38 chr3: 156,552,750-156,552,750 , GRCh38 chr3: 156,552,837-156,552,837 , GRCh37.p13 chr3: 156,270,626-156,270,626 , GRCh37.p13 chr3: 156,270,539-156,270,539 SSR3
    nsv5033132inversion1nstd200human GRCh38 chr3: 147,205,794-180,217,342 , GRCh37.p13 chr3: 146,923,581-179,935,130 , LOC105374154, 433 more genes
    nsv4684209copy number variation1nstd102humanPathogenic GRCh37 chr3: 138,145,289-162,275,610 , GRCh38.p12 chr3: 138,426,447-162,557,822 MTAPP1, PLS1, 339 more genes
    nsv4674662copy number variation1nstd102humanUncertain significance GRCh37 chr3: 156,194,709-156,591,239 , GRCh38.p12 chr3: 156,476,920-156,873,450 LEKR1, LINC00886, 6 more genes
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