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Items: 1 to 20 of 276

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148253copy number variation1nstd102humanPathogenic GRCh38 chr8: 449,893-23,854,904 , GRCh37.p13 chr8: 399,893-23,712,417 ENTPD4, LOC100421446, 447 more genes
    nsv7148146copy number variation1nstd102humanPathogenic GRCh38 chr8: 12,721,809-30,183,737 , GRCh37.p13 chr8: 12,579,318-30,041,253 LOC101929028, RPL35P6, 274 more genes
    nsv7076380inversion1nstd229human GRCh38 chr8: 13,445,918-15,932,362 , GRCh37.p13 chr8: 13,303,427-15,789,871 TUSC3, EIF4EP5, 15 more genes
    nsv7074647inversion1nstd229human GRCh38 chr8: 11,585,028-14,417,119 , GRCh37.p13 chr8: 11,442,537-14,274,628 RNU7-153P, OR7E8P, 79 more genes
    nsv7072516inversion1nstd229human GRCh38 chr8: 13,441,627-15,436,149 , GRCh37.p13 chr8: 13,299,136-15,293,658 LOC100419761, LOC100421673, 12 more genes
    nsv7070898inversion1nstd229human GRCh38 chr8: 13,526,786-14,826,198 , GRCh37.p13 chr8: 13,384,295-14,683,707 EIF4EP5, DLC1, 11 more genes
    nsv7067873inversion1nstd229human GRCh38 chr8: 13,535,845-13,643,447 , GRCh37.p13 chr8: 13,393,354-13,500,956 C8orf48, LOC102725080, 3 more genes
    nsv7065354inversion1nstd229human GRCh38 chr8: 9,129,798-15,405,439 , GRCh37.p13 chr8: 8,987,308-15,262,948 FAM167A, LOC729732, 132 more genes
    nsv7065207inversion1nstd229human GRCh38 chr8: 13,508,278-14,431,845 , GRCh37.p13 chr8: 13,365,787-14,289,354 EIF4EP5, DLC1, 10 more genes
    nsv7059349inversion1nstd229human GRCh38 chr8: 13,516,160-14,431,844 , GRCh37.p13 chr8: 13,373,669-14,289,353 LOC102725080, LOC100419761, 10 more genes
    nsv6857256copy number variation1nstd229human GRCh38 chr8: 13,465,633-13,766,167 , GRCh37.p13 chr8: 13,323,142-13,623,676 DLC1, RNA5SP255, 4 more genes
    nsv6855221copy number variation1nstd229human GRCh38 chr8: 13,554,836-13,574,642 , GRCh37.p13 chr8: 13,412,345-13,432,151 DLC1, C8orf48
    nsv6852642copy number variation1nstd229human GRCh38 chr8: 13,551,521-13,669,750 , GRCh37.p13 chr8: 13,409,030-13,527,259 LOC102725080, C8orf48, 2 more genes
    nsv6851500copy number variation1nstd229human GRCh38 chr8: 13,565,701-13,586,900 , GRCh37.p13 chr8: 13,423,210-13,444,409 C8orf48, LOC100421023, 1 more genes
    nsv6844376copy number variation1nstd229human GRCh38 chr8: 13,525,736-14,057,883 , GRCh37.p13 chr8: 13,383,245-13,915,392 DLC1, RNA5SP255, 7 more genes
    nsv6842473copy number variation1nstd229human GRCh38 chr8: 13,341,295-13,721,604 , GRCh37.p13 chr8: 13,198,804-13,579,113 C8orf48, LOC102725080, 5 more genes
    nsv6839939copy number variation1nstd229human GRCh38 chr8: 13,540,901-13,729,782 , GRCh37.p13 chr8: 13,398,410-13,587,291 DLC1, C8orf48, 2 more genes
    nsv6839911copy number variation1nstd229human GRCh38 chr8: 12,834,229-13,806,691 , GRCh37.p13 chr8: 12,691,738-13,664,200 LOC100419761, C8orf48, 10 more genes
    nsv6838968copy number variation1nstd229human GRCh38 chr8: 13,507,981-13,609,017 , GRCh37.p13 chr8: 13,365,490-13,466,526 DLC1, LOC100421023, 2 more genes
    nsv6636968copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,049-18,936,715 , GRCh38.p12 chr8: 208,049-19,079,205 ZNF705B, NATP, 357 more genes
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