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Items: 1 to 20 of 1151

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv2667872copy number variation147estd199human GRCh37 chr1: 225,133,630-225,248,654 , GRCh38.p12 chr1: 224,945,928-225,060,952 DNAH14
    esv2670203copy number variation158estd199human GRCh37 chr6: 78,967,194-79,036,475 , GRCh38.p12 chr6: 78,257,477-78,326,758 LOC105377865
    esv2663818copy number variation78estd199human GRCh37 chr10: 47,897,245-47,959,492 , GRCh38.p12 chr10: 50,081,347-50,143,571 WASHC2A
    esv2676879copy number variation198estd199human GRCh37 chr4: 34,779,980-34,829,038 , GRCh38.p12 chr4: 34,778,358-34,827,416 , GRCh38.p12 chr4|NW_003315915.1: 270,687-319,745 LOC105378262
    esv2660251copy number variation7estd199human GRCh37 chr5: 101,166,760-101,207,359 , GRCh38.p12 chr5: 101,831,056-101,871,655 LOC105379102
    esv2666277copy number variation79estd199human GRCh37 chr7: 141,765,351-141,794,383 , GRCh38.p12 chr7: 142,065,551-142,094,583 , GRCh38.p12 chr7|NT_187562.1: 27,431-56,463 MGAM
    esv2661219copy number variation458estd199human GRCh37 chr8: 48,180,445-48,214,692 , GRCh38.p12 chr8: 47,276,396-47,302,103 SPIDR
    esv2666901copy number variation459estd199human GRCh37 chr11: 1,915,249-1,937,009 , GRCh38.p12 chr11: 1,894,019-1,915,779 LINC01150
    esv2669475copy number variation624estd199human GRCh37 chr1: 147,976,045-147,996,192 , GRCh38.p12 chr1: 120,848,940-120,869,086 RNVU1-19
    esv2672554copy number variation26estd199human GRCh37 chr8: 75,312,945-75,330,192 , GRCh38.p12 chr8: 74,400,710-74,417,957 GDAP1
    esv2665073copy number variation1estd199human GRCh37 chr2: 31,942,884-31,958,456 , GRCh38.p12 chr2: 31,717,815-31,733,387 LOC107985862
    esv2670177copy number variation26estd199human GRCh37 chr17: 1,475,742-1,490,977 , GRCh38.p12 chr17: 1,572,448-1,587,683 , GRCh38.p12 chr17|NT_187611.1: 2,476-17,711 SLC43A2
    esv2671576copy number variation156estd199human GRCh37 chr7: 100,326,645-100,341,192 , GRCh38.p12 chr7: 100,729,022-100,743,569 ZAN
    esv2675305copy number variation21estd199human GRCh37 chr22: 28,186,245-28,200,392 , GRCh38.p12 chr22: 27,790,257-27,804,404 MN1
    esv2664165copy number variation220estd199human GRCh37 chr7: 100,327,572-100,340,716 , GRCh38.p12 chr7: 100,729,949-100,743,093 ZAN
    esv2670618copy number variation111estd199human GRCh37 chr11: 89,495,739-89,507,199 , GRCh38.p12 chr11: 89,762,571-89,774,031 TRIM49
    esv2669961copy number variation4estd199human GRCh37 chr12: 69,022,377-69,033,179 , GRCh38.p12 chr12: 68,628,597-68,639,399 RAP1B
    esv2656977copy number variation38estd199human GRCh37 chr19: 548,645-559,392 , GRCh38.p12 chr19: 548,645-559,392 GZMM
    esv2660610copy number variation9estd199human GRCh37 chr6: 160,627,750-160,638,096 , GRCh38.p12 chr6: 160,206,718-160,217,064 SLC22A2
    esv2661214copy number variation77estd199human GRCh37 chr12: 133,516,945-133,527,192 , GRCh38.p12 chr12: 132,940,359-132,950,606 ZNF605
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