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Items: 1 to 20 of 297

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5968823insertion1nstd209human GRCh38 chr15: 79,199,698-79,199,698 , GRCh37.p13 chr15: 79,492,040-79,492,040 ANKRD34C-AS1
    nsv5944527copy number variation1nstd209human GRCh38 chr15: 79,284,242-79,284,303 , GRCh37.p13 chr15: 79,576,584-79,576,645 ANKRD34C, ANKRD34C-AS1
    nsv5941927copy number variation1nstd209human GRCh38 chr15: 79,192,258-79,192,316 , GRCh37.p13 chr15: 79,484,600-79,484,658 ANKRD34C-AS1
    nsv5940009copy number variation1nstd209human GRCh38 chr15: 79,256,022-79,262,332 , GRCh37.p13 chr15: 79,548,364-79,554,674 ANKRD34C-AS1
    nsv5935349copy number variation1nstd209human GRCh38 chr15: 77,970,674-82,312,707 , GRCh37.p13 chr15: 78,263,016-82,605,043 , ST20, 91 more genes
    nsv5933606copy number variation1nstd209human GRCh38 chr15: 71,577,714-80,433,232 , GRCh37.p13 chr15: 71,870,053-80,725,573 , STRA6, 229 more genes
    nsv5858250copy number variation1nstd209human GRCh38 chr15: 79,255,725-79,260,145 , GRCh37.p13 chr15: 79,548,067-79,552,487 ANKRD34C-AS1
    nsv5849741copy number variation1nstd209human GRCh38 chr15: 79,256,025-79,262,325 , GRCh37.p13 chr15: 79,548,367-79,554,667 ANKRD34C-AS1
    nsv5531429copy number variation1nstd206human GRCh38 chr15: 79,203,862-79,204,123 , GRCh37.p13 chr15: 79,496,204-79,496,465 ANKRD34C-AS1
    nsv5517670copy number variation1nstd206human GRCh38 chr15: 79,256,022-79,262,333 , GRCh37.p13 chr15: 79,548,364-79,554,675 ANKRD34C-AS1
    nsv5514627copy number variation1nstd206human GRCh38 chr15: 79,229,747-79,230,134 , GRCh37.p13 chr15: 79,522,089-79,522,476 ANKRD34C-AS1
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5349206translocation1nstd200human GRCh38 chr15: 79,252,347-79,252,347 , GRCh38 chr15: 79,252,427-79,252,427 , GRCh37.p13 chr15: 79,544,689-79,544,689 , GRCh37.p13 chr15: 79,544,769-79,544,769 ANKRD34C-AS1
    nsv5329930translocation1nstd200human GRCh37 chr15: 79,484,605-79,484,605 , GRCh37 chr15: 79,484,659-79,484,659 , GRCh38.p12 chr15: 79,192,263-79,192,263 , GRCh38.p12 chr15: 79,192,317-79,192,317 ANKRD34C-AS1
    nsv5152345mobile element insertion1nstd203human GRCh38 chr15: 79,233,117-79,233,125 , GRCh37.p13 chr15: 79,525,459-79,525,467 ANKRD34C-AS1
    nsv5009085copy number variation1nstd200human GRCh38 chr15: 79,203,862-79,204,123 , GRCh37.p13 chr15: 79,496,204-79,496,465 ANKRD34C-AS1
    nsv5001903copy number variation1nstd200human GRCh38 chr15: 79,256,022-79,262,333 , GRCh37.p13 chr15: 79,548,364-79,554,675 ANKRD34C-AS1
    nsv5001902copy number variation1nstd200human GRCh38 chr15: 79,207,159-79,212,791 , GRCh37.p13 chr15: 79,499,501-79,505,133 MIR184, ANKRD34C-AS1
    nsv4992298copy number variation1nstd200human GRCh38 chr15: 73,152,590-82,101,178 , GRCh37.p13 chr15: 73,444,931-82,393,519 , SNUPN, 215 more genes
    nsv4863907copy number variation1nstd200human GRCh37 chr15: 79,496,204-79,496,465 , GRCh38.p12 chr15: 79,203,862-79,204,123 ANKRD34C-AS1
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