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Items: 1 to 20 of 253

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7059980inversion1nstd229human GRCh38 chr20: 30,656,049-33,860,963 , GRCh37.p13 chr20: 29,803,910-32,448,769 NECAB3, EFCAB8, 98 more genes
    nsv7037901copy number variation1nstd229human GRCh38 chr20: 31,423,301-31,739,500 , GRCh37.p13 chr20: 30,011,104-30,327,303 BCL2L1, DEFB123, 18 more genes
    nsv7036625copy number variation1nstd229human GRCh38 chr20: 31,678,281-31,678,380 , GRCh37.p13 chr20: 30,266,084-30,266,183 BCL2L1-AS1, BCL2L1
    nsv7034522copy number variation1nstd229human GRCh38 chr20: 31,666,087-31,721,653 , GRCh37.p13 chr20: 30,253,890-30,309,456 ABALON, BCL2L1, 1 more genes
    nsv7032549copy number variation1nstd229human GRCh38 chr20: 31,308,013-31,715,090 , GRCh37.p13 chr20: 29,895,816-30,302,893 TRS-AGA7-1, ID1, 24 more genes
    nsv7028912copy number variation1nstd229human GRCh38 chr20: 31,628,818-31,672,293 , GRCh37.p13 chr20: 30,216,621-30,260,096 BCL2L1, COX4I2
    nsv7028699copy number variation1nstd229human GRCh38 chr20: 31,712,863-31,713,216 , GRCh37.p13 chr20: 30,300,666-30,301,019 BCL2L1-AS1, BCL2L1
    nsv7028519copy number variation1nstd229human GRCh38 chr20: 31,720,570-31,720,767 , GRCh37.p13 chr20: 30,308,373-30,308,570 ABALON, BCL2L1
    nsv7028368copy number variation1nstd229human GRCh38 chr20: 31,579,910-33,642,127 , GRCh37.p13 chr20: 30,167,713-32,229,933 PLAGL2, BPIFB4, 57 more genes
    nsv7025136copy number variation1nstd229human GRCh38 chr20: 31,456,221-31,905,173 , GRCh37.p13 chr20: 30,044,024-30,492,976 COX4I2, CD24P3, 21 more genes
    nsv7023421copy number variation1nstd229human GRCh38 chr20: 31,687,697-31,691,159 , GRCh37.p13 chr20: 30,275,500-30,278,962 BCL2L1-AS1, BCL2L1
    nsv7023310copy number variation1nstd229human GRCh38 chr20: 31,719,807-31,719,923 , GRCh37.p13 chr20: 30,307,610-30,307,726 ABALON, BCL2L1
    nsv7020692copy number variation1nstd229human GRCh38 chr20: 31,713,834-31,791,445 , GRCh37.p13 chr20: 30,301,637-30,379,248 BCL2L1, TPX2, 2 more genes
    nsv6637725copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 29,833,535-34,815,537 , GRCh38.p12 chr20: 31,245,732-36,227,615 AHCY, ASIP, 160 more genes
    nsv6637546copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 29,652,122-35,603,726 , GRCh38.p12 chr20: 30,417,446-36,975,323 AHCY, ASIP, 195 more genes
    nsv6637514copy number variation1nstd102humanUncertain significance GRCh37 chr20: 30,299,729-30,687,587 , GRCh38.p12 chr20: 31,711,926-32,099,784 RNA5SP482, TTLL9, 13 more genes
    nsv6599418inversion1nstd223human GRCh38 chr20: 31,693,220-31,693,814 , GRCh37.p13 chr20: 30,281,023-30,281,617 BCL2L1-AS1, BCL2L1
    nsv6531299copy number variation1nstd223human GRCh38 chr20: 31,687,696-31,691,157 , GRCh37.p13 chr20: 30,275,499-30,278,960 BCL2L1, BCL2L1-AS1
    nsv6313956copy number variation1nstd102humanPathogenic GRCh37 chr20: 25,442,597-33,761,550 , GRCh38.p12 chr20: 25,461,961-35,173,747 LOC105372586, RNU6-384P, 193 more genes
    nsv6291672copy number variation1nstd102humanLikely benign GRCh37 chr20: 29,652,122-30,272,637 , GRCh38.p12 chr20: 30,417,446-31,684,834 DEFB124, LOC105379481, 47 more genes
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