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Items: 1 to 20 of 189

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148263copy number variation1nstd102humanPathogenic GRCh38 chr9: 102,995,214-108,903,040 , GRCh37.p13 chr9: 105,757,496-111,665,320 ACTL7B, OR13C3, 88 more genes
    nsv6878046copy number variation1nstd229human GRCh38 chr9: 104,076,672-104,093,458 , GRCh37.p13 chr9: 106,838,953-106,855,739 SMC2-DT, SMC2
    nsv6874764copy number variation1nstd229human GRCh38 chr9: 104,085,388-104,221,148 , GRCh37.p13 chr9: 106,847,669-106,983,429 SMC2, SMC2-DT
    nsv6871470copy number variation1nstd229human GRCh38 chr9: 104,077,295-104,081,494 , GRCh37.p13 chr9: 106,839,576-106,843,775 SMC2-DT
    nsv6868318copy number variation1nstd229human GRCh38 chr9: 104,081,076-104,114,535 , GRCh37.p13 chr9: 106,843,357-106,876,816 SMC2, SMC2-DT
    nsv6867844copy number variation1nstd229human GRCh38 chr9: 104,080,175-104,084,831 , GRCh37.p13 chr9: 106,842,456-106,847,112 SMC2-DT
    nsv6866765copy number variation1nstd229human GRCh38 chr9: 104,078,392-104,091,616 , GRCh37.p13 chr9: 106,840,673-106,853,897 SMC2-DT
    nsv6866297copy number variation1nstd229human GRCh38 chr9: 104,078,296-104,083,472 , GRCh37.p13 chr9: 106,840,577-106,845,753 SMC2-DT
    nsv6865867copy number variation1nstd229human GRCh38 chr9: 103,223,858-104,260,467 , GRCh37.p13 chr9: 105,986,140-107,022,748 LINC03094, SMC2-DT, 5 more genes
    nsv6865617copy number variation1nstd229human GRCh38 chr9: 104,050,471-104,090,030 , GRCh37.p13 chr9: 106,812,752-106,852,311 SMC2-DT
    nsv6859827copy number variation1nstd229human GRCh38 chr9: 103,996,376-104,175,957 , GRCh37.p13 chr9: 106,758,657-106,938,238 LINC03094, SMC2, 2 more genes
    nsv6637573copy number variation1nstd102humanUncertain significance GRCh37 chr9: 106,173,402-107,431,515 , GRCh38.p12 chr9: 103,411,120-104,669,234 LOC105376194, TOPORSLP, 18 more genes
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6439915copy number variation1nstd223human GRCh38 chr9: 104,050,471-104,090,026 , GRCh37.p13 chr9: 106,812,752-106,852,307 SMC2-DT
    nsv6315405copy number variation1nstd102humanUncertain significance GRCh37 chr9: 19,356,861-119,513,311 , GRCh38.p12 chr9: 19,356,863-116,751,032 RNU6-156P, GDA, 1425 more genes
    nsv6313900copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 71,349,994-122,603,410 , GRCh38.p12 chr9: 68,735,078-119,841,132 ABCA1, ALAD, 793 more genes
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
    nsv6303771copy number variation1nstd186human GRCh37 chr9: 106,812,752-106,852,307 , GRCh38.p12 chr9: 104,050,471-104,090,026 SMC2-DT
    nsv6290765copy number variation1nstd102humanUncertain significance GRCh37 chr9: 102,858,276-110,624,997 , GRCh38.p12 chr9: 100,095,994-107,862,716 RNF20, SMC2, 120 more genes
    nsv6137322copy number variation1nstd213human GRCh37 chr9: 106,780,000-107,030,001 , GRCh38.p12 chr9: 104,017,719-104,267,720 SMC2, SMC2-DT
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