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Items: 1 to 20 of 153

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5370075translocation1nstd200human GRCh38 chr7: 524,065-524,065 , GRCh38 chr7: 523,985-523,985 , GRCh37.p13 chr7: 563,622-563,622 , GRCh37.p13 chr7: 563,702-563,702 PDGFA-DT
    nsv4679604copy number variation1nstd189human GRCh37.p13 chr7: 518,519-745,398 , GRCh38.p12 chr7: 478,882-705,761 PDGFA, PRKAR1B, 4 more genes
    nsv4675871copy number variation1nstd102humanPathogenic GRCh37 chr7: 44,935-1,750,797 , GRCh38.p12 chr7: 44,935-1,711,161 C7orf50, LOC105375123, 47 more genes
    nsv4675301copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,360-1,648,288 , GRCh38.p12 chr7: 43,360-1,608,652 LOC112267991, MICALL2, 42 more genes
    nsv4609020copy number variation1nstd183human GRCh37 chr7: 558,700-559,900 , GRCh38.p12 chr7: 519,063-520,263 PDGFA, PDGFA-DT
    nsv4456827copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,376-19,520,619 , GRCh38.p12 chr7: 43,376-19,480,996 MIR6836, EEF1A1P26, 277 more genes
    nsv4456136copy number variation1nstd102humanPathogenic GRCh37 chr7: 36,616-4,298,168 , GRCh38.p12 chr7: 36,616-4,258,536 LOC442497, LFNG, 85 more genes
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 RPL23AP51, FLJ40288, 2684 more genes
    nsv4376782copy number variation1nstd173human GRCh37 chr7: 230,908-941,749 , GRCh38.p12 chr7: 230,908-902,112 PRKAR1B-AS1, LOC105375119, 15 more genes
    nsv3961959insertion1nstd168human GRCh37.p13 chr7: 493,948-668,178 , GRCh38 chr7: 454,071-628,541 PDGFA, PRKAR1B, 4 more genes
    nsv3924805copy number variation1nstd102humanUncertain significance NCBI36 chr7: 324,907-607,447 , GRCh37.p13 chr7: 229,824-640,921 , GRCh38.p12 chr7: 229,824-601,284 LOC105375118, FOXL3-OT1, 10 more genes
    nsv3924345copy number variation1nstd102humanPathogenic NCBI36 chr7: 149,248-731,488 , GRCh38 chr7: 54,165-725,325 , GRCh37 chr7: 54,165-764,962 PRKAR1B, LOC105375114, 19 more genes
    nsv3923348copy number variation1nstd102humanPathogenic NCBI36 chr7: 149,268-6,644,183 , GRCh37 chr7: 54,185-6,677,658 , GRCh38 chr7: 54,185-6,638,027 ZNF890P, FOXK1, 143 more genes
    nsv3923236copy number variation1nstd102humanUncertain significance GRCh37 chr7: 54,185-1,370,682 , NCBI36 chr7: 149,268-1,337,208 , GRCh38 chr7: 54,185-1,331,046 PDGFA-DT, C7orf50, 33 more genes
    nsv3922329copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,360-27,236,023 , GRCh38 chr7: 43,360-27,196,404 , NCBI36 chr7: 138,443-27,202,548 LOC401312, IQCE, 411 more genes
    nsv3921351copy number variation1nstd102humanPathogenic GRCh37 chr7: 45,130-6,309,816 , GRCh38 chr7: 45,130-6,270,185 , NCBI36 chr7: 140,213-6,276,341 ELFN1, LINC02983, 131 more genes
    nsv3920326copy number variation1nstd102humanUncertain significance GRCh38 chr7: 45,130-821,632 , NCBI36 chr7: 140,213-827,795 , GRCh37 chr7: 45,130-861,269 LOC105375115, LOC101929756, 20 more genes
    nsv3920006copy number variation1nstd102humanPathogenic GRCh37 chr7: 45,130-5,920,006 , GRCh38 chr7: 45,130-5,880,375 , NCBI36 chr7: 140,213-5,886,532 RNU6-215P, NUDT1, 120 more genes
    nsv3919826copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840 RNU6-438P, LOC105375300, 2682 more genes
    nsv3919613copy number variation1nstd102humanPathogenic GRCh38 chr7: 45,130-7,252,065 , NCBI36 chr7: 140,213-7,258,221 , GRCh37 chr7: 45,130-7,291,696 LOC105375115, ZNF890P, 161 more genes
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