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Items: 1 to 20 of 31

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3877767copy number variation1nstd102humanLikely benign GRCh37 chr2: 158,183,948-158,300,390 , GRCh38.p12 chr2: 157,327,436-157,443,878 CYTIP, FAM133DP, 1 more genes
    nsv3910630copy number variation1nstd102humanPathogenic NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331 CYTIP, DAZAP2P1, 2991 more genes
    nsv3898306copy number variation1nstd102humanPathogenic GRCh38 chr2: 148,917,286-163,204,623 , GRCh37 chr2: 149,674,855-164,061,133 , NCBI36 chr2: 149,391,325-163,769,379 CYTIP, RPS3AP13, 170 more genes
    nsv3877758copy number variation1nstd102humanPathogenic GRCh37 chr2: 157,970,774-169,270,675 , GRCh38.p12 chr2: 157,114,262-168,414,165 CYTIP, GCA, 121 more genes
    nsv4674226copy number variation1nstd102humanPathogenic GRCh37 chr2: 147,173,792-158,346,266 , GRCh38.p12 chr2: 146,416,224-157,489,754 CYTIP, RBM43, 120 more genes
    nsv3902718copy number variation1nstd102humanPathogenic GRCh38 chr2: 147,251,948-157,856,378 , NCBI36 chr2: 147,725,986-158,421,136 , GRCh37 chr2: 148,009,516-158,712,890 CYTIP, RNU6-1275P, 117 more genes
    nsv3921316copy number variation1nstd102humanPathogenic NCBI36 chr2: 155,624,215-165,414,901 , GRCh37.p13 chr2: 155,915,969-165,706,655 , GRCh38.p12 chr2: 155,059,457-164,850,145 CYTIP, LOC105373712, 121 more genes
    nsv3894168copy number variation1nstd102humanPathogenic GRCh37 chr2: 152,788,858-160,276,245 , GRCh38 chr2: 151,932,344-159,419,734 , NCBI36 chr2: 152,497,104-159,984,491 CYTIP, RNU6-1001P, 88 more genes
    nsv3910092copy number variation1nstd102humanPathogenic NCBI36 chr2: 152,138,015-159,100,037 , GRCh37.p13 chr2: 152,429,769-159,391,791 , GRCh38.p12 chr2: 151,573,255-158,535,279 CYTIP, ACVR1C, 73 more genes
    nsv3922653copy number variation1nstd102humanPathogenic NCBI36 chr2: 154,499,404-159,392,834 , GRCh37.p13 chr2: 154,791,158-159,684,588 , GRCh38.p12 chr2: 153,934,645-158,828,076 CYTIP, CCDC148, 59 more genes
    nsv3892461copy number variation1nstd102humanPathogenic GRCh37 chr2: 154,466,227-159,041,637 , GRCh38 chr2: 153,609,714-158,185,125 , NCBI36 chr2: 154,174,473-158,749,883 CYTIP, RNU6-1001P, 53 more genes
    nsv6291446copy number variation1nstd102humanPathogenic GRCh37 chr2: 154,328,530-158,759,642 , GRCh38.p12 chr2: 153,472,016-157,903,130 CYTIP, RNU6-1001P, 47 more genes
    nsv6291000copy number variation1nstd102humanPathogenic GRCh37 chr2: 154,852,961-159,126,250 , GRCh38.p12 chr2: 153,996,448-158,269,738 CYTIP, LINC01876, 52 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 CYTIP, LOC112268439, 3737 more genes
    nsv3874648copy number variation1nstd102humanPathogenic GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305 CYTIP, IGKV2OR2-10, 3737 more genes
    nsv3885544copy number variation1nstd102humanPathogenic GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609 CYTIP, RNU6-674P, 3735 more genes
    nsv3882615copy number variation2nstd102humanPathogenic GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232 CYTIP, MTND2P22, 3724 more genes
    nsv3875392copy number variation1nstd102humanPathogenic GRCh37 chr2: 152,409,978-179,325,736 , GRCh38.p12 chr2: 151,553,464-178,461,009 CYTIP, MIR10B, 359 more genes
    nsv3874278copy number variation1nstd102humanPathogenic GRCh37 chr2: 156,489,430-182,921,298 , GRCh38.p12 chr2: 155,632,918-182,056,571 CYTIP, LOC107985957, 358 more genes
    nsv3893853copy number variation1nstd102humanPathogenic GRCh38 chr2: 154,294,042-175,989,372 , GRCh37 chr2: 155,150,555-176,854,100 , NCBI36 chr2: 154,858,801-176,562,346 CYTIP, SCN7A, 275 more genes
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