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Items: 1 to 20 of 191

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148130copy number variation1nstd102humanPathogenic GRCh37 chr8: 36,763,176-50,929,707 , GRCh38.p12 chr8: 36,905,658-50,017,147 SNTG1, RN7SL806P, 193 more genes
    nsv6632642copy number variation1nstd224human GRCh37 chr8: 47,173,274-48,423,371 , GRCh38.p12 chr8: 46,261,652-47,510,809 RPL10AP2, MAPK6P4, 30 more genes
    nsv6313701copy number variation1nstd102humanUncertain significance GRCh37 chr8: 42,162,574-48,757,095 , GRCh38.p12 chr8: 42,305,056-47,844,534 RNU1-124P, LOC728587, 66 more genes
    nsv6277832insertion1nstd214human GRCh38 chr8: 46,853,915-46,853,915 , GRCh37.p13 chr8: 47,765,537-47,765,537 LINC00293
    nsv6136682copy number variation1nstd213human GRCh37 chr8: 47,250,000-47,860,001 , GRCh38.p12 chr8: 46,338,378-46,948,379 ASNSP1, LINC00293, 15 more genes
    nsv6136681copy number variation1nstd213human GRCh37 chr8: 46,860,000-86,550,001 , GRCh38.p12 chr8: 45,948,378-85,637,772 CEBPD, EYA1, 519 more genes
    nsv5917461copy number variation1nstd209human GRCh38 chr8: 41,299,580-47,196,853 , GRCh37.p13 chr8: 41,157,099-48,108,476 , AFG3L2P1, 81 more genes
    nsv5371617translocation1nstd200human GRCh38 chr8: 46,839,679-46,839,679 , GRCh38 chr8: 46,839,730-46,839,730 , GRCh37.p13 chr8: 47,751,301-47,751,301 , GRCh37.p13 chr8: 47,751,352-47,751,352 LINC00293, MTND6P20
    nsv4952058copy number variation1nstd200human GRCh38 chr8: 46,838,832-46,839,082 , GRCh37.p13 chr8: 47,750,454-47,750,704 MTCYBP20, LINC00293, 1 more genes
    nsv4952057copy number variation1nstd200human GRCh38 chr8: 46,837,896-46,843,021 , GRCh37.p13 chr8: 47,749,518-47,754,643 MTND6P20, LINC00293, 1 more genes
    nsv4952052copy number variation1nstd200human GRCh38 chr8: 46,779,397-46,861,908 , GRCh37.p13 chr8: 47,691,019-47,773,530 LOC100130861, MTND1P7, 8 more genes
    nsv4812927copy number variation1nstd200human GRCh37 chr8: 47,691,019-47,773,530 , GRCh38.p12 chr8: 46,779,397-46,861,908 TRIM60P15, MTND1P7, 8 more genes
    nsv4768211inversion1nstd199human GRCh37 chr8: 23,474,464-53,327,098 , GRCh38.p12 chr8: 23,616,951-52,414,538 , ADRA1A, 411 more genes
    nsv4756879inversion1nstd199human GRCh37 chr8: 23,474,453-53,323,933 , GRCh38.p12 chr8: 23,616,940-52,411,373 , ADRA1A, 411 more genes
    nsv4709817copy number variation1nstd195human GRCh37 chr8: 47,747,451-47,806,201 , GRCh38.p12 chr8: 46,835,829-46,894,579 LINC00293, LOC728587, 3 more genes
    nsv4709804copy number variation1nstd195human GRCh37 chr8: 47,747,601-47,806,401 , GRCh38.p12 chr8: 46,835,979-46,894,779 LINC00293, LOC728587, 3 more genes
    nsv4680431copy number variation1nstd189human GRCh37.p13 chr8: 46,847,535-47,780,554 , GRCh38.p12 chr8: 45,935,913-46,868,932 ASNSP1, LINC00293, 13 more genes
    nsv4614291copy number variation1nstd183human GRCh37 chr8: 47,750,734-47,804,607 , GRCh38.p12 chr8: 46,839,112-46,892,985 LOC105375813, LINC00293, 3 more genes
    nsv4611972copy number variation1nstd183human GRCh37 chr8: 46,847,534-48,392,708 , GRCh38.p12 chr8: 45,935,912-47,480,146 LOC105375816, NDUFA5P12, 29 more genes
    nsv4606338copy number variation1nstd183human GRCh37 chr8: 47,766,892-47,769,782 , GRCh38.p12 chr8: 46,855,270-46,858,160 LINC00293
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