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Items: 1 to 20 of 542

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142661copy number variation1nstd232human GRCh37.p13 chr8: 143,601,683-143,601,759 , GRCh38.p12 chr8: 142,520,322-142,520,398 ADGRB1
    nsv7139774copy number variation1nstd232human GRCh37.p13 chr8: 143,583,089-143,583,258 , GRCh38.p12 chr8: 142,501,728-142,501,897 ADGRB1
    nsv7077766inversion1nstd229human GRCh38 chr8: 142,544,830-142,549,826 , GRCh37.p13 chr8: 143,626,191-143,631,187 ADGRB1
    nsv7076973inversion1nstd229human GRCh38 chr8: 142,464,504-142,464,705 , GRCh37.p13 chr8: 143,545,865-143,546,066 ADGRB1
    nsv7076080inversion1nstd229human GRCh38 chr8: 137,223,456-143,780,837 , GRCh37.p13 chr8: 138,235,699-144,743,525 LOC107986906, FAM83H, 108 more genes
    nsv7061615inversion1nstd229human GRCh38 chr8: 139,238,401-143,070,465 , GRCh37.p13 chr8: 140,250,644-144,151,882 PEG13, LINC01300, 63 more genes
    nsv6876670copy number variation1nstd229human GRCh38 chr8: 142,449,867-142,457,848 , GRCh37.p13 chr8: 143,531,228-143,539,209 ADGRB1
    nsv6864399copy number variation1nstd229human GRCh38 chr8: 142,458,331-142,459,975 , GRCh37.p13 chr8: 143,539,692-143,541,336 ADGRB1
    nsv6862354copy number variation1nstd229human GRCh38 chr8: 142,511,519-142,512,117 , GRCh37.p13 chr8: 143,592,880-143,593,478 ADGRB1
    nsv6861932copy number variation1nstd229human GRCh38 chr8: 141,966,201-142,462,600 , GRCh37.p13 chr8: 143,047,562-143,543,961 LOC105375792, LINC00051, 5 more genes
    nsv6861480copy number variation1nstd229human GRCh38 chr8: 142,528,623-142,528,668 , GRCh37.p13 chr8: 143,609,984-143,610,029 ADGRB1
    nsv6861295copy number variation1nstd229human GRCh38 chr8: 142,449,701-142,617,700 , GRCh37.p13 chr8: 143,531,062-143,699,061 MROH4P, ARC, 1 more genes
    nsv6637631copy number variation1nstd102humanUncertain significance GRCh37 chr8: 142,836,592-144,175,046 , GRCh38.p12 chr8: 141,755,231-143,093,629 CYP11B1, LOC105375792, 33 more genes
    nsv6634360copy number variation1nstd102humanPathogenic GRCh37 chr8: 68,912,432-146,295,771 , GRCh38.p12 chr8: 68,000,197-145,070,385 WASHC5, LOC100132280, 1028 more genes
    nsv6558189inversion1nstd223human GRCh38 chr8: 142,217,754-142,483,322 , GRCh37.p13 chr8: 143,299,115-143,564,683 ADGRB1, TSNARE1, 1 more genes
    nsv6434466copy number variation1nstd223human GRCh38 chr8: 142,501,623-142,501,731 , GRCh37.p13 chr8: 143,582,984-143,583,092 ADGRB1
    nsv6429467copy number variation1nstd223human GRCh38 chr8: 142,481,916-142,482,322 , GRCh37.p13 chr8: 143,563,277-143,563,683 ADGRB1
    nsv6425776copy number variation1nstd223human GRCh38 chr8: 142,482,001-142,483,300 , GRCh37.p13 chr8: 143,563,362-143,564,661 ADGRB1
    nsv6425142copy number variation1nstd223human GRCh38 chr8: 142,504,201-142,505,700 , GRCh37.p13 chr8: 143,585,562-143,587,061 ADGRB1
    nsv6417526copy number variation1nstd223human GRCh38 chr8: 142,256,520-142,935,362 , GRCh37.p13 chr8: 143,337,881-144,016,778 ZNHIT1P1, MROH4P, 19 more genes
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