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Items: 1 to 20 of 251

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148161copy number variation1nstd102humanPathogenic GRCh38 chr4: 1-49,062,177 , GRCh37.p13 chr4: 507,005-49,064,194 SLIRPP2, STIM2-AS1, 659 more genes
    nsv7148157copy number variation1nstd102humanPathogenic GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396 OR7E84P, FAM193A, 764 more genes
    nsv6735396copy number variation1nstd229human GRCh38 chr4: 46,946,997-46,948,820 , GRCh37.p13 chr4: 46,949,014-46,950,837 GABRA4
    nsv6734928copy number variation1nstd229human GRCh38 chr4: 46,989,501-47,020,800 , GRCh37.p13 chr4: 46,991,518-47,022,817 GABRA4, GABRB1
    nsv6732663copy number variation1nstd229human GRCh38 chr4: 46,919,801-46,988,300 , GRCh37.p13 chr4: 46,921,818-46,990,317 GABRA4
    nsv6726840copy number variation1nstd229human GRCh38 chr4: 46,919,601-46,988,400 , GRCh37.p13 chr4: 46,921,618-46,990,417 GABRA4
    nsv6726423copy number variation1nstd229human GRCh38 chr4: 46,913,389-47,072,269 , GRCh37.p13 chr4: 46,915,406-47,074,286 GABRA4, GABRB1
    nsv6634358copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-49,089,361 , GRCh38.p12 chr4: 68,453-49,087,344 LINC02475, LOC105374344, 658 more genes
    nsv6395079copy number variation1nstd223human GRCh38 chr4: 46,975,475-46,976,072 , GRCh37.p13 chr4: 46,977,492-46,978,089 GABRA4
    nsv6389148copy number variation1nstd223human GRCh38 chr4: 46,960,101-46,960,900 , GRCh37.p13 chr4: 46,962,118-46,962,917 GABRA4
    nsv6388940copy number variation1nstd223human GRCh38 chr4: 46,927,460-46,927,968 , GRCh37.p13 chr4: 46,929,477-46,929,985 GABRA4
    nsv6388866copy number variation1nstd223human GRCh38 chr4: 46,988,757-46,989,381 , GRCh37.p13 chr4: 46,990,774-46,991,398 GABRA4
    nsv6386655copy number variation1nstd223human GRCh38 chr4: 46,928,701-46,929,800 , GRCh37.p13 chr4: 46,930,718-46,931,817 GABRA4
    nsv6384255copy number variation1nstd223human GRCh38 chr4: 46,932,379-46,932,734 , GRCh37.p13 chr4: 46,934,396-46,934,751 GABRA4
    nsv6381485copy number variation1nstd223human GRCh38 chr4: 46,939,294-46,939,731 , GRCh37.p13 chr4: 46,941,311-46,941,748 GABRA4
    nsv6380785copy number variation1nstd223human GRCh38 chr4: 46,944,639-46,945,027 , GRCh37.p13 chr4: 46,946,656-46,947,044 GABRA4
    nsv6377644copy number variation1nstd223human GRCh38 chr4: 46,979,576-46,980,124 , GRCh37.p13 chr4: 46,981,593-46,982,141 GABRA4
    nsv6315440copy number variation1nstd102humanPathogenic GRCh37 chr4: 114,784-47,569,569 , GRCh38.p12 chr4: 114,902-47,567,552 FAM86KP, ENPP7P11, 631 more genes
    nsv6311833copy number variation1nstd102humanUncertain significance GRCh37 chr4: 46,252,325-47,163,506 , GRCh38.p12 chr4: 46,250,308-47,161,489 GABRA4, GABRB1, 4 more genes
    nsv6279164insertion1nstd214human GRCh38 chr4: 46,972,289-46,972,289 , GRCh37.p13 chr4: 46,974,306-46,974,306 GABRA4
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