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Items: 1 to 20 of 1214

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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
    esv2674748copy number variation32estd199human GRCh37 chr14: 41,603,645-41,664,592 , GRCh38.p12 chr14: 41,134,440-41,195,389 LINC02315
    esv2665996copy number variation112estd199human 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
    esv2668226copy number variation311estd199human GRCh37 chr3: 129,763,245-129,799,692 , GRCh38.p12 chr3: 130,044,402-130,080,849 ALG1L2
    esv2673583copy number variation519estd199human GRCh37 chr20: 1,560,991-1,594,041 , GRCh38.p12 chr20: 1,580,345-1,613,395 SIRPB1
    esv2676662copy number variation263estd199human GRCh37 chr19: 41,360,712-41,392,496 , GRCh38.p12 chr19: 40,854,807-40,886,591 CYP2A7
    esv2672539copy number variation26estd199human GRCh37 chrX: 102,778,956-102,809,126 , GRCh38.p12 chrX: 103,524,028-103,554,198 LINC02589
    esv2667697copy number variation42estd199human GRCh37 chr7: 141,765,556-141,794,588 , GRCh38.p12 chr7: 142,065,756-142,094,788 , GRCh38.p12 chr7|NT_187562.1: 27,636-56,668 MGAM
    esv2669475copy number variation624estd199human GRCh37 chr1: 147,976,045-147,996,192 , GRCh38.p12 chr1: 120,848,940-120,869,086 RNVU1-19
    esv2662901copy number variation324estd199human GRCh37 chr9: 41,969,445-41,984,392 , GRCh38.p12 chr9: 39,824,427-39,839,374 FGF7P3
    esv2663811copy number variation483estd199human GRCh37 chr7: 133,785,000-133,798,329 , GRCh38.p12 chr7: 134,100,247-134,113,576
    esv2656701copy number variation437estd199human GRCh37 chr16: 78,371,638-78,384,898 , GRCh38.p12 chr16: 78,337,741-78,351,001 WWOX
    esv2664803copy number variation436estd199human GRCh37 chr15: 76,884,596-76,896,938 , GRCh38.p12 chr15: 76,592,255-76,604,597 SCAPER
    esv2678677copy number variation179estd199human GRCh37 chr15: 76,884,295-76,895,742 , GRCh38.p12 chr15: 76,591,954-76,603,401 SCAPER
    esv2664044copy number variation84estd199human GRCh37 chr15: 56,789,861-56,801,000 , GRCh38.p12 chr15: 56,497,663-56,508,802
    esv2674298copy number variation219estd199human GRCh37 chr1: 35,101,421-35,111,976 , GRCh38.p12 chr1: 34,635,820-34,646,375 LOC105378641
    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
    esv2662536copy number variation311estd199human GRCh37 chr6: 72,863,851-72,873,540 , GRCh38.p12 chr6: 72,154,148-72,163,837 RIMS1
    esv2661768copy number variation445estd199human GRCh37 chr5: 12,811,019-12,820,535 , GRCh38.p12 chr5: 12,810,907-12,820,423 LOC105374657
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