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Items: 1 to 20 of 173

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6129435insertion1nstd186human GRCh37 chr17: 79,650,667-79,650,704 , GRCh38.p12 chr17: 81,683,637-81,683,674 HGS, ARL16
    nsv5701380mobile element insertion2nstd211human GRCh38 chr17: 81,683,637-81,683,637 , GRCh37.p13 chr17: 79,650,667-79,650,667 HGS, ARL16
    nsv5536199insertion1nstd206human GRCh38 chr17: 81,683,637-81,683,674 , GRCh37.p13 chr17: 79,650,667-79,650,704 HGS, ARL16
    nsv5361801translocation1nstd200human GRCh38 chr1: 52,032,326-52,032,326 , GRCh38 chr17: 81,683,763-81,683,763 , GRCh37.p13 chr1: 52,497,998-52,497,998 , GRCh37.p13 chr17: 79,650,793-79,650,793 HGS, TXNDC12, 2 more genes
    nsv5361799translocation1nstd200human GRCh38 chr1: 52,032,326-52,032,326 , GRCh38 chr17: 81,683,126-81,683,126 , GRCh37.p13 chr1: 52,497,998-52,497,998 , GRCh37.p13 chr17: 79,650,156-79,650,156 HGS, TXNDC12, 2 more genes
    nsv5298108copy number variation1nstd204human GRCh38.p13 chr17: 80,930,501-82,586,000 , GRCh37.p13 chr17: 78,904,301-80,543,876 , PPP1R27, 89 more genes
    nsv5287926copy number variation1nstd204human GRCh38.p13 chr17: 81,643,901-81,742,500 , GRCh37.p13 chr17: 79,610,927-79,709,049 MRPL12, OXLD1, 8 more genes
    nsv5148152mobile element insertion1nstd203human GRCh38 chr17: 81,683,623-81,683,637 , GRCh37.p13 chr17: 79,650,653-79,650,667 ARL16, HGS
    nsv5017044copy number variation1nstd200human GRCh38 chr17: 81,441,456-81,816,579 , GRCh37.p13 chr17: 79,498,418-79,774,455 , LOC105376789, 19 more genes
    nsv4717755mobile element insertion1nstd186human GRCh37 chr17: 79,650,653-79,650,653 , GRCh38.p12 chr17: 81,683,623-81,683,623 HGS, ARL16
    nsv4689331mobile element insertion1nstd186human GRCh37 chr17: 79,650,671-79,650,671 , GRCh38.p12 chr17: 81,683,641-81,683,641 HGS, ARL16
    nsv4628884copy number variation1nstd183human GRCh37 chr17: 79,650,896-79,651,148 , GRCh38.p12 chr17: 81,683,866-81,684,118 HGS, ARL16
    nsv4625921copy number variation1nstd183human GRCh37 chr17: 78,632,841-79,703,517 , GRCh38.p12 chr17: 80,659,041-81,736,487 , HGS, 44 more genes
    nsv4501149mobile element insertion1nstd166human GRCh37.p13 chr17: 79,650,653-79,650,653 , GRCh38.p12 chr17: 81,683,623-81,683,623 HGS, ARL16
    nsv4457646copy number variation1nstd102humanPathogenic GRCh37 chr17: 62,778,720-81,041,938 , GRCh38.p12 chr17: 64,782,602-83,084,062 LOC107985089, ARSG, 448 more genes
    nsv4457616copy number variation1nstd102humanUncertain significance GRCh37 chr17: 79,496,613-79,693,150 , GRCh38.p12 chr17: 81,529,587-81,726,120 MRPL12, ARL16, 10 more genes
    nsv4457483copy number variation1nstd102humanPathogenic GRCh37 chr17: 78,608,912-81,041,938 , GRCh38.p12 chr17: 80,635,112-83,084,062 HEXD, LOC105371929, 94 more genes
    nsv4457456copy number variation1nstd102humanUncertain significance GRCh37 chr17: 79,531,886-79,685,043 , GRCh38.p12 chr17: 81,564,860-81,718,013 SLC25A10, MRPL12, 8 more genes
    nsv4374349copy number variation1nstd173human GRCh37 chr17: 79,330,617-80,189,678 , GRCh38.p12 chr17: 81,356,817-82,231,802 , FAAP100, 49 more genes
    nsv3919635copy number variation1nstd102humanPathogenic GRCh37 chr17: 76,088,317-81,044,553 , NCBI36 chr17: 73,599,912-78,637,842 , GRCh38 chr17: 78,092,236-83,086,677 LINC03048, MIR3186, 154 more genes
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