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Items: 1 to 20 of 132

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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
    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
    nsv6724097copy number variation1nstd229human GRCh38 chr3: 155,859,341-156,259,331 , GRCh37.p13 chr3: 155,577,130-155,977,120 GMPS, SNRNP40P1, 7 more genes
    nsv6722682copy number variation1nstd229human GRCh38 chr3: 156,225,746-156,230,807 , GRCh37.p13 chr3: 155,943,535-155,948,596 KCNAB1-AS2, KCNAB1
    nsv6721477copy number variation1nstd229human GRCh38 chr3: 156,105,073-156,313,612 , GRCh37.p13 chr3: 155,822,862-156,031,401 KCNAB1, KCNAB1-AS2, 2 more genes
    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
    nsv6628658copy number variation1nstd224human GRCh37 chr3: 155,597,745-156,039,826 , GRCh38.p12 chr3: 155,879,956-156,322,037 MRE11P1, KCNAB1, 6 more genes
    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
    nsv6313775copy number variation1nstd102humanUncertain significance GRCh37 chr3: 155,774,023-155,935,321 , GRCh38.p12 chr3: 156,056,234-156,217,532 KCNAB1, KCNAB1-AS2, 2 more genes
    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
    nsv6259846mobile element insertion1nstd215human GRCh38 chr3: 156,228,323-156,228,323 , GRCh37.p13 chr3: 155,946,112-155,946,112 KCNAB1-AS2, KCNAB1
    nsv6259845mobile element insertion1nstd215human GRCh38 chr3: 156,218,803-156,218,803 , GRCh37.p13 chr3: 155,936,592-155,936,592 KCNAB1-AS2, KCNAB1
    nsv6134788copy number variation1nstd213human GRCh37 chr3: 155,010,000-169,630,001 , GRCh38.p12 chr3: 155,292,211-169,912,213 , BCHE, 171 more genes
    nsv5691010mobile element insertion1nstd211human GRCh38 chr3: 156,222,334-156,222,334 , GRCh37.p13 chr3: 155,940,123-155,940,123 KCNAB1, KCNAB1-AS2
    nsv5400546mobile element insertion1nstd206human GRCh38 chr3: 156,222,334-156,222,385 , GRCh37.p13 chr3: 155,940,123-155,940,174 KCNAB1, KCNAB1-AS2
    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
    nsv5098725mobile element insertion1nstd203human GRCh38 chr3: 156,222,320-156,222,334 , GRCh37.p13 chr3: 155,940,109-155,940,123 KCNAB1-AS2, KCNAB1
    nsv5033132inversion1nstd200human GRCh38 chr3: 147,205,794-180,217,342 , GRCh37.p13 chr3: 146,923,581-179,935,130 , LOC105374154, 433 more genes
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