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Items: 1 to 20 of 230

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5971545inversion1nstd209human GRCh38 chr16: 34,285,151-37,946,447 , GRCh37.p13 chr16: 34,191,257-46,500,513 , GRCh37.p13 chr7: 61,054,333-64,968,441 , FRG2DP, 75 more genes
    nsv5945080copy number variation1nstd209human GRCh38 chr16: 34,256,335-36,325,869 , GRCh37.p13 chr16: 34,173,152-35,285,801 , NAMPTP3, 76 more genes
    nsv5943102copy number variation1nstd209human GRCh38 chr16: 34,919,547-36,186,973 , GRCh37.p13 chr16: 34,174,183-35,285,801 , UBE2MP1, 70 more genes
    nsv5942260copy number variation1nstd209human GRCh38 chr16: 34,272,628-37,335,777 , GRCh37.p13 chr7: 61,054,333-64,968,441 , RNA5SP409, 75 more genes
    nsv5885862copy number variation2nstd209human GRCh38 chr16: 35,746,940-35,748,539 , GRCh37.p13 chr16: 34,981,311-34,982,910 LINC02167, RNA5SP412, 4 more genes
    nsv5315457copy number variation1nstd204human GRCh38.p13 chr16: 35,176,373-36,133,971 , GRCh37.p13 chr16: 34,410,744-35,285,810 C2orf69P4, LINC02167, 57 more genes
    nsv5003782copy number variation1nstd200human GRCh38 chr16: 35,688,183-35,780,235 , GRCh37.p13 chr16: 34,922,554-35,014,606 RNA5SP419, RNA5SP422, 17 more genes
    nsv4994792copy number variation1nstd200human GRCh38 chr16: 35,176,378-36,133,962 , GRCh37.p13 chr16: 34,410,749-35,285,801 RNA5SP415, FGFR3P5, 57 more genes
    nsv4761426inversion1nstd199human GRCh37 chr16: 34,197,021-46,500,376 , GRCh38.p12 chr16: 34,962,650-46,466,464 , FRG2DP, 70 more genes
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    nsv4730119inversion62nstd198human GRCh38 chr16: 34,459,624-46,410,119 , GRCh37.p13 chr16: 34,173,152-46,444,031 , FRG2DP, 70 more genes
    nsv4680819copy number variation1nstd189human GRCh37.p13 chr1: 149,024,803-149,758,041 , GRCh38.p12 chr16: 34,885,225-36,219,524 , FRG2DP, 70 more genes
    nsv4680404copy number variation1nstd189human GRCh37.p13 chr1: 149,024,803-149,772,497 , GRCh38.p12 chr16: 34,885,225-36,219,524 , FRG2DP, 70 more genes
    nsv4680201copy number variation1nstd189human GRCh37.p13 chr16: 34,197,352-35,283,226 , GRCh38.p12 chr16: 34,962,981-36,048,855 , FRG2DP, 69 more genes
    nsv4680085copy number variation1nstd189human GRCh37.p13 chr1: 148,893,346-149,758,041 , GRCh38.p12 chr16: 34,881,439-36,215,339 , GRCh38.p12 chr7: 61,006,478-62,429,617 , FRG2DP, 70 more genes
    nsv4679813copy number variation1nstd189human GRCh37.p13 chr1: 148,747,654-149,702,535 , GRCh38.p12 chr16: 34,686,966-36,217,241 , GRCh38.p12 chr7: 61,006,478-62,429,617 , FRG2DP, 70 more genes
    nsv4679020copy number variation1nstd189human GRCh37.p13 chr1: 148,858,446-149,702,535 , GRCh38.p12 chr16: 34,634,079-36,215,335 , GRCh38.p12 chr7: 61,006,478-62,429,617 , FRG2DP, 70 more genes
    nsv4678936copy number variation1nstd189human GRCh37.p13 chr16: 34,212,701-35,283,226 , GRCh38.p12 chr16: 34,978,330-36,048,855 , FRG2DP, 69 more genes
    nsv4626955copy number variation1nstd183human GRCh37 chr16: 34,197,351-35,283,226 , GRCh38.p12 chr16: 34,962,980-36,048,855 , HMGN2P41, 69 more genes
    nsv4624591copy number variation1nstd183human GRCh37 chr16: 34,774,476-35,283,226 , GRCh38.p12 chr16: 35,540,105-36,048,855 RARRES2P8, RNA5SP415, 25 more genes
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