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Items: 1 to 20 of 120

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7071535inversion1nstd229human GRCh38 chr9: 124,246,999-128,875,010 , GRCh37.p13 chr9: 127,009,278-131,637,289 PTGES2-AS1, STXBP1, 130 more genes
    nsv6875698copy number variation1nstd229human GRCh38 chr9: 127,442,217-127,447,145 , GRCh37.p13 chr9: 130,204,496-130,209,424 ZNF79, RPL12, 1 more genes
    nsv6868491copy number variation1nstd229human GRCh38 chr9: 127,440,814-127,446,421 , GRCh37.p13 chr9: 130,203,093-130,208,700 ZNF79, RPL12
    nsv6865544copy number variation1nstd229human GRCh38 chr9: 127,441,701-127,523,300 , GRCh37.p13 chr9: 130,203,980-130,285,579 SNORA65, NIBAN2, 3 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
    nsv6452382copy number variation1nstd223human GRCh38 chr9: 127,416,554-127,472,639 , GRCh37.p13 chr9: 130,178,833-130,234,918 LRSAM1, SNORA65, 2 more genes
    nsv6446995copy number variation1nstd223human GRCh38 chr9: 127,442,211-127,447,144 , GRCh37.p13 chr9: 130,204,490-130,209,423 SNORA65, ZNF79, 1 more genes
    nsv6445995copy number variation1nstd223human GRCh38 chr9: 127,409,601-127,469,900 , GRCh37.p13 chr9: 130,171,880-130,232,179 SNORA65, ZNF79, 2 more genes
    nsv6445830copy number variation1nstd223human GRCh38 chr9: 127,317,501-128,138,900 , GRCh37.p13 chr9: 130,079,780-130,901,179 STXBP1, PTGES2-AS1, 34 more genes
    nsv6438803copy number variation1nstd223human GRCh38 chr9: 126,485,301-128,649,400 , GRCh37.p13 chr9: 129,247,580-131,411,679 MIR199B, FPGS, 72 more genes
    nsv6314001copy number variation1nstd102humanPathogenic GRCh37 chr9: 116,422,275-131,713,233 , GRCh38.p12 chr9: 113,659,995-128,950,954 LOC105376244, RN7SL187P, 286 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
    nsv6291261copy number variation1nstd102humanPathogenic GRCh37 chr9: 128,523,763-132,604,808 , GRCh38.p12 chr9: 125,761,484-129,842,529 PTPA, AK1, 123 more genes
    nsv6137056copy number variation1nstd213human GRCh37 chr9: 130,190,000-130,360,001 , GRCh38.p12 chr9: 127,427,721-127,597,722 RPL12, ZNF79, 4 more genes
    nsv5564479copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr9: 129,376,729-131,016,993 , GRCh38.p12 chr9: 126,614,450-128,254,714 PIP5KL1, MIR3911, 50 more genes
    nsv5040732inversion1nstd200human GRCh38 chr9: 100,673,006-127,581,711 , GRCh37.p13 chr9: 103,435,288-130,343,990 , LOC105379839, 440 more genes
    nsv4768372copy number variation1nstd102humanPathogenic GRCh37 chr9: 128,512,347-130,702,572 , GRCh38.p12 chr9: 125,750,068-127,940,293 LOC105379841, PTRH1, 47 more genes
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4455186copy number variation1nstd102humanPathogenic GRCh37 chr9: 71,416,475-141,020,389 , GRCh38.p12 chr9: 68,801,559-138,125,937 LOC105376327, ENG, 1304 more genes
    nsv4337085sequence alteration1nstd166human GRCh37.p13 chr9: 91,988,635-138,279,888 , GRCh38.p12 chr9: 89,373,720-135,388,042 , ABCA1, 927 more genes
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