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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    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
    esv2666739copy number variation325estd199human GRCh37 chr1: 207,699,545-207,737,892 , GRCh38.p12 chr1: 207,526,200-207,564,547 CR1
    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
    esv2669475copy number variation624estd199human GRCh37 chr1: 147,976,045-147,996,192 , GRCh38.p12 chr1: 120,848,940-120,869,086 RNVU1-19
    esv2663133copy number variation46estd199human GRCh37 chr6: 32,629,745-32,648,392 , GRCh38.p12 chr6: 32,661,968-32,680,615 HLA-DQB1
    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
    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
    esv2678677copy number variation179estd199human GRCh37 chr15: 76,884,295-76,895,742 , GRCh38.p12 chr15: 76,591,954-76,603,401 SCAPER
    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
    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
    esv2664029copy number variation6estd199human GRCh37 chr7: 148,632,945-148,642,392 , GRCh38.p12 chr7: 148,935,853-148,945,300 RNY5
    esv2668452copy number variation609estd199human GRCh37 chr6: 165,724,666-165,732,132 , GRCh38.p12 chr6: 165,311,177-165,318,643 LOC105378113
    esv2664161copy number variation195estd199human GRCh37 chr11: 55,031,599-55,038,540 , GRCh38.p12 chr11: 55,264,123-55,271,064 TRIM48
    esv2672397copy number variation68estd199human GRCh37 chr3: 2,305,514-2,312,433 , GRCh38.p12 chr3: 2,263,830-2,270,749 CNTN4
    esv2657591copy number variation82estd199human GRCh37 chr12: 86,426,103-86,432,915 , GRCh38.p12 chr12: 86,032,325-86,039,137 MGAT4C
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