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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3872646copy number variation1nstd102humanLikely pathogenic GRCh38 chr2: 205,264,941-205,497,509 , GRCh37.p13 chr2: 206,129,665-206,362,233 PARD3B
    nsv3872051copy number variation1nstd102humanLikely pathogenic GRCh38 chr2: 205,102,232-205,198,713 , GRCh37.p13 chr2: 205,966,956-206,063,437 PARD3B
    nsv3885951copy number variation1nstd102humanBenign GRCh37 chr2: 206,128,178-206,129,889 , GRCh38.p12 chr2: 205,263,454-205,265,165 PARD3B
    nsv3880160copy number variation1nstd102humanBenign GRCh37 chr2: 206,096,536-206,131,317 , GRCh38.p12 chr2: 205,231,812-205,266,593 PARD3B
    nsv3914406copy number variation1nstd102humanUncertain significance NCBI36 chr2: 206,036,885-206,189,405 , GRCh37.p13 chr2: 206,328,640-206,481,160 , GRCh38.p12 chr2: 205,463,916-205,616,436 PARD3B
    nsv6636885copy number variation1nstd102humanUncertain significance GRCh37 chr2: 205,519,961-205,638,704 , GRCh38.p12 chr2: 204,655,238-204,773,981 PARD3B
    nsv4453534copy number variation2nstd102humanUncertain significance GRCh37 chr2: 205,519,998-205,638,704 , GRCh38.p12 chr2: 204,655,275-204,773,981 PARD3B
    nsv6636369copy number variation1nstd102humanUncertain significance GRCh37 chr2: 205,519,999-205,638,704 , GRCh38.p12 chr2: 204,655,276-204,773,981 PARD3B
    nsv3874189copy number variation1nstd102humanLikely benign GRCh37 chr2: 205,801,070-206,805,019 , GRCh38.p12 chr2: 204,936,347-205,940,295 PARD3B, RN7SKP178, 2 more genes
    nsv4453441copy number variation1nstd102humanUncertain significance GRCh37 chr2: 204,858,354-205,794,074 , GRCh38.p12 chr2: 203,993,631-204,929,351 PARD3B, DSTNP5, 3 more genes
    nsv4452397copy number variation1nstd102humanUncertain significance GRCh37 chr2: 205,800,577-206,805,019 , GRCh38.p12 chr2: 204,935,854-205,940,295 PARD3B, NRP2, 2 more genes
    nsv3910630copy number variation1nstd102humanPathogenic NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331 PARD3B, DAZAP2P1, 2991 more genes
    nsv6315398copy number variation1nstd102humanPathogenic GRCh37 chr2: 185,697,659-213,002,074 , GRCh38.p12 chr2: 184,832,932-212,137,349 PARD3B, LOC107985785, 381 more genes
    nsv3896612copy number variation1nstd102humanPathogenic GRCh38 chr2: 192,938,826-215,705,052 , NCBI36 chr2: 193,511,797-216,278,020 , GRCh37 chr2: 193,803,552-216,569,775 PARD3B, MTND4P30, 320 more genes
    nsv6637127copy number variation1nstd102humanPathogenic GRCh37 chr2: 189,909,904-209,468,383 , GRCh38.p12 chr2: 189,045,178-208,603,658 PARD3B, LOC100421409, 310 more genes
    nsv3903696copy number variation1nstd102humanPathogenic NCBI36 chr2: 200,510,241-210,604,893 , GRCh37 chr2: 200,801,996-210,896,648 , GRCh38 chr2: 199,937,273-210,031,924 PARD3B, MTND4P23, 206 more genes
    nsv3895332copy number variation1nstd102humanPathogenic GRCh37 chr2: 200,811,217-210,849,919 , GRCh38 chr2: 199,946,494-209,985,195 , NCBI36 chr2: 200,519,462-210,558,164 PARD3B, CCNYL1, 203 more genes
    nsv6313730copy number variation1nstd102humanPathogenic GRCh37 chr2: 200,851,079-209,054,267 , GRCh38.p12 chr2: 199,986,356-208,189,543 PARD3B, RN7SKP200, 179 more genes
    nsv4728545copy number variation1nstd102humanPathogenic GRCh37 chr2: 204,445,619-212,580,788 , GRCh38.p12 chr2: 203,580,896-211,716,063 PARD3B, FASTKD2, 110 more genes
    nsv3892523copy number variation1nstd102humanPathogenic GRCh37 chr2: 205,771,566-210,896,173 , NCBI36 chr2: 205,479,811-210,604,418 , GRCh38 chr2: 204,906,843-210,031,449 PARD3B, SNORD51, 84 more genes
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