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Items: 1 to 20 of 4351

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5587994copy number variation1nstd207human GRCh38 chr19: 40,833,931-40,864,823 , GRCh37.p13 chr19: 41,339,836-41,370,728 CYP2A6
    nsv5566484copy number variation1nstd207human GRCh38 chr8: 43,308,569-43,328,260 , GRCh37.p13 chr8: 43,163,712-43,183,403 POTEA
    nsv5585078copy number variation1nstd207human GRCh38 chr17: 38,145,459-38,162,319 , GRCh37.p13 chr17|NW_003315949.1: 226,111-242,954 LOC102723933
    nsv5573493copy number variation1nstd207human GRCh38 chr1: 210,428,015-210,440,838 , GRCh37.p13 chr1: 210,601,359-210,614,182 HHAT
    nsv5574749copy number variation1nstd207human GRCh38 chr8: 16,404,542-16,417,174 , GRCh37.p13 chr8: 16,262,051-16,274,683 LOC101929028
    nsv5572875copy number variation1nstd207human GRCh38 chr4: 53,203,252-53,215,869 , GRCh37.p13 chr4: 54,069,419-54,082,036 SCFD2
    nsv5581782copy number variation1nstd207human GRCh38 chr7: 76,515,456-76,527,665 , GRCh37.p13 chr7: 76,144,773-76,156,982 UPK3B
    nsv5586656copy number variation1nstd207human GRCh38 chr10: 79,617,422-79,627,798 , GRCh37.p13 chr10: 81,377,178-81,387,554 LINC02679
    nsv5600765copy number variation1nstd207human GRCh38 chr12: 44,879,387-44,889,702 , GRCh37.p13 chr12: 45,273,170-45,283,485 NELL2
    nsv5578774copy number variation1nstd207human GRCh38 chr2: 43,855,636-43,865,926 , GRCh37.p13 chr2: 44,082,775-44,093,065 ABCG8
    nsv5586810copy number variation1nstd207human GRCh38 chr16: 76,627,603-76,637,180 , GRCh37.p13 chr16: 76,661,500-76,671,077 LINC02125
    nsv5565954copy number variation1nstd207human GRCh38 chr5: 156,658,538-156,666,749 , GRCh37.p13 chr5: 156,085,549-156,093,760 SGCD
    nsv5603067copy number variation1nstd207human GRCh38 chr10: 73,614,031-73,621,428 , GRCh37.p13 chr10: 75,373,789-75,381,186 USP54
    nsv5601008copy number variation1nstd207human GRCh38 chr12: 86,301,927-86,309,285 , GRCh37.p13 chr12: 86,695,705-86,703,063 MGAT4C
    nsv5577140copy number variation1nstd207human GRCh38 chr8: 50,118,531-50,125,728 , GRCh37.p13 chr8: 51,031,091-51,038,288 SNTG1
    nsv5573333copy number variation1nstd207human GRCh38 chr1: 77,308,834-77,315,903 , GRCh37.p13 chr1: 77,774,519-77,781,588 AK5
    nsv5572752copy number variation1nstd207human GRCh38 chr6: 121,198,315-121,204,804 , GRCh37.p13 chr6: 121,519,461-121,525,950 TBC1D32
    nsv5566823copy number variation1nstd207human GRCh38 chr1: 189,802,318-189,808,629 , GRCh37.p13 chr1: 189,771,448-189,777,759 LINC01701
    nsv5581190copy number variation1nstd207human GRCh38 chr6: 147,117,255-147,123,288 , GRCh37.p13 chr6: 147,438,391-147,444,424 STXBP5-AS1
    nsv5574183copy number variation1nstd207human GRCh38 chr5: 156,521,329-156,527,245 , GRCh37.p13 chr5: 155,948,339-155,954,255 SGCD
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