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Items: 1 to 20 of 160

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7060339inversion1nstd229human GRCh38 chr20: 23,599,888-23,883,729 , GRCh37.p13 chr20: 23,580,525-23,864,366 CST9, CST1, 9 more genes
    nsv7035921copy number variation1nstd229human GRCh38 chr20: 23,407,997-23,871,822 , GRCh37.p13 chr20: 23,388,634-23,852,459 CST12P, CST8, 17 more genes
    nsv7032175copy number variation1nstd229human GRCh38 chr20: 23,493,451-23,727,872 , GRCh37.p13 chr20: 23,474,088-23,708,509 LOC107985383, CST4, 8 more genes
    nsv7032011copy number variation1nstd229human GRCh38 chr20: 23,203,457-24,359,303 , GRCh37.p13 chr20: 23,184,094-24,339,939 CST9, RNU1-23P, 32 more genes
    nsv7029901copy number variation1nstd229human GRCh38 chr20: 23,522,540-24,257,872 , GRCh37.p13 chr20: 23,503,177-24,238,508 POM121L3P, CST4, 20 more genes
    nsv7027175copy number variation1nstd229human GRCh38 chr20: 23,666,392-23,712,451 , GRCh37.p13 chr20: 23,647,029-23,693,088 CST4, LOC107985383
    nsv7025942copy number variation1nstd229human GRCh38 chr20: 23,664,614-24,244,066 , GRCh37.p13 chr20: 23,645,251-24,224,702 WAKMAR1, RNU1-23P, 14 more genes
    nsv7021176copy number variation1nstd229human GRCh38 chr20: 23,662,047-24,080,303 , GRCh37.p13 chr20: 23,642,684-24,060,939 CSTP1, CST1, 11 more genes
    nsv7020679copy number variation1nstd229human GRCh38 chr20: 23,393,385-24,073,730 , GRCh37.p13 chr20: 23,374,022-24,054,367 LOC107985438, CSTP2, 22 more genes
    nsv6637732copy number variation1nstd102humanUncertain significance GRCh37 chr20: 23,142,478-24,824,349 , GRCh38.p12 chr20: 23,161,841-24,843,713 NAPB, POM121L3P, 37 more genes
    nsv6626756copy number variation1nstd224human GRCh37 chr20: 23,663,817-23,700,824 , GRCh38.p12 chr20: 23,683,180-23,720,187 CST4
    nsv6626754copy number variation1nstd224human GRCh37 chr20: 23,375,624-24,052,857 , GRCh38.p12 chr20: 23,394,987-24,072,220 CST5, GGTLC1, 22 more genes
    nsv6626753copy number variation1nstd224human GRCh37 chr20: 23,369,317-24,042,329 , GRCh38.p12 chr20: 23,388,680-24,061,692 CST3, CSTP2, 22 more genes
    nsv6626553copy number variation1nstd224human GRCh37 chr20: 23,669,472-23,731,494 , GRCh38.p12 chr20: 23,688,835-23,750,857 LOC105372574, CST1, 1 more genes
    nsv6626552copy number variation1nstd224human GRCh37 chr20: 23,656,525-23,700,824 , GRCh38.p12 chr20: 23,675,888-23,720,187 CST4
    nsv6626551copy number variation1nstd224human GRCh37 chr20: 23,594,292-23,860,259 , GRCh38.p12 chr20: 23,613,655-23,879,622 CST1, CST4, 8 more genes
    nsv6535408copy number variation1nstd223human GRCh38 chr20: 23,666,392-23,712,447 , GRCh37.p13 chr20: 23,647,029-23,693,084 CST4, LOC107985383
    nsv6526119copy number variation1nstd223human GRCh38 chr20: 23,679,263-23,810,364 , GRCh37.p13 chr20: 23,659,900-23,791,001 LOC105372575, CSTP2, 4 more genes
    nsv6515791copy number variation1nstd223human GRCh38 chr20: 23,685,903-23,747,999 , GRCh37.p13 chr20: 23,666,540-23,728,636 CST1, CST4, 1 more genes
    nsv6291578copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 18,665,879-33,903,216 , GRCh38.p12 chr20: 18,685,235-35,315,413 AHCY, ASIP, 330 more genes
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