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Items: 1 to 20 of 1564

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv2676574copy number variation189estd199human GRCh37 chr6: 78,967,194-79,036,497 , GRCh38.p12 chr6: 78,257,477-78,326,780 LOC105377865
    esv2670203copy number variation158estd199human GRCh37 chr6: 78,967,194-79,036,475 , GRCh38.p12 chr6: 78,257,477-78,326,758 LOC105377865
    esv2676068copy number variation152estd199human GRCh37 chr6: 32,454,245-32,511,792 , GRCh38.p12 chr6: 32,486,468-32,544,015 HLA-DRB5
    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
    esv2666618copy number variation41estd199human GRCh37 chr11: 49,709,802-49,757,715 , GRCh38.p12 chr11: 49,688,250-49,736,163 , GRCh38.p12 chr11|NW_019805495.1: 152,431-200,312 GRM5P1
    esv2672105copy number variation71estd199human GRCh37 chr20: 1,553,045-1,594,292 , GRCh38.p12 chr20: 1,572,399-1,613,646 SIRPB1
    esv2660522copy number variation236estd199human GRCh37 chr1: 207,700,012-207,737,123 , GRCh38.p12 chr1: 207,526,667-207,563,778 CR1
    esv2668226copy number variation311estd199human GRCh37 chr3: 129,763,245-129,799,692 , GRCh38.p12 chr3: 130,044,402-130,080,849 ALG1L2
    esv2676662copy number variation263estd199human GRCh37 chr19: 41,360,712-41,392,496 , GRCh38.p12 chr19: 40,854,807-40,886,591 CYP2A7
    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
    esv2657599copy number variation40estd199human GRCh37 chr9: 44,742,045-44,764,392 , GRCh38.p12 chr9: 61,534,207-61,556,554 LOC105379437
    esv2661915copy number variation81estd199human GRCh37 chr6: 77,437,226-77,458,987 , GRCh38.p12 chr6: 76,727,509-76,749,270 LOC105377861
    esv2674235copy number variation67estd199human GRCh37 chr2: 98,139,745-98,158,992 , GRCh38.p12 chr2: 97,523,282-97,542,529 ANKRD36B
    esv2669960copy number variation208estd199human GRCh37 chr9: 41,968,745-41,984,492 , GRCh38.p12 chr9: 39,823,727-39,839,474 FGF7P3
    esv2670787copy number variation158estd199human GRCh37 chr7: 151,134-160,557 , GRCh38.p12 chr7: 151,134-160,557 , GRCh38.p12 chr7|NT_187558.1: 106,939-119,904 , GRCh38.p12 chr7|NT_187653.1: 143,455-152,878 LINC03014
    esv2673551copy number variation872estd199human GRCh37 chr3: 192,875,329-192,885,405 , GRCh38.p12 chr3: 193,157,540-193,167,616 VEZF1P1
    esv2675979copy number variation520estd199human GRCh37 chr6: 53,924,803-53,934,828 , GRCh38.p12 chr6: 54,060,005-54,070,030 MLIP
    esv2673070copy number variation52estd199human GRCh37 chr9: 139,667,329-139,677,234 , GRCh38.p12 chr9: 136,772,877-136,782,782 ATP6V1G1P3
    esv2657260copy number variation826estd199human GRCh37 chr2: 87,730,745-87,740,792 , GRCh38.p12 chr2: 87,431,226-87,441,083 LINC01943
    esv2662536copy number variation311estd199human GRCh37 chr6: 72,863,851-72,873,540 , GRCh38.p12 chr6: 72,154,148-72,163,837 RIMS1
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