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Items: 1 to 20 of 140

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4729080copy number variation1nstd102humanUncertain significance GRCh37 chr6: 14,590,996-16,067,315 , GRCh38.p12 chr6: 14,590,765-16,067,084 LOC105374946, LOC105374949, 16 more genes
    nsv4728994copy number variation1nstd102humanUncertain significance GRCh37 chr6: 15,062,578-15,371,639 , GRCh38.p12 chr6: 15,062,347-15,371,408 RNU6-645P, RPL6P17, 5 more genes
    nsv4675138copy number variation1nstd102humanUncertain significance GRCh37 chr6: 15,177,338-15,382,780 , GRCh38.p12 chr6: 15,177,107-15,382,549 LOC105374946, RNU6-522P, 3 more genes
    nsv4598387copy number variation1nstd183human GRCh37 chr6: 15,248,316-15,249,040 , GRCh38.p12 chr6: 15,248,085-15,248,809 JARID2, JARID2-AS1
    nsv4598386copy number variation1nstd183human GRCh37 chr6: 14,845,071-15,433,896 , GRCh38.p12 chr6: 14,844,840-15,433,665 , JARID2, 7 more genes
    nsv4457139copy number variation1nstd102humanUncertain significance GRCh37 chr6: 14,715,955-17,223,929 , GRCh38.p12 chr6: 14,715,724-17,223,698 MDH1P2, ATXN1, 28 more genes
    nsv4456780copy number variation1nstd102humanPathogenic GRCh37 chr6: 156,974-23,221,621 , GRCh38.p12 chr6: 156,974-23,221,393 LOC105374960, LOC101928573, 342 more genes
    nsv4456299copy number variation1nstd102humanPathogenic GRCh37 chr6: 13,910,125-22,000,204 , GRCh38.p12 chr6: 13,909,894-21,999,975 LOC101928354, MBOAT1, 101 more genes
    nsv4455888copy number variation1nstd102humanUncertain significance GRCh37 chr6: 13,248,587-18,083,552 , GRCh38.p12 chr6: 13,248,355-18,083,321 RNU6-522P, LOC105374942, 70 more genes
    nsv4394167copy number variation1nstd174human GRCh37 chr6: 15,248,316-15,249,040 , GRCh38.p12 chr6: 15,248,085-15,248,809 JARID2, JARID2-AS1
    nsv3922769copy number variation1nstd102humanUncertain significance NCBI36 chr6: 14,653,555-16,171,002 , GRCh38 chr6: 14,545,345-16,062,792 , GRCh37 chr6: 14,545,576-16,063,023 ARPC3P5, RNU6-522P, 16 more genes
    nsv3922594copy number variation1nstd102humanPathogenic GRCh37 chr6: 13,311,751-16,295,791 , GRCh38 chr6: 13,311,519-16,295,560 , NCBI36 chr6: 13,419,730-16,403,770 LOC107986571, LOC105374947, 47 more genes
    nsv3922052copy number variation1nstd102humanPathogenic GRCh37 chr6: 155,807-17,058,645 , NCBI36 chr6: 100,807-17,166,624 , GRCh38 chr6: 155,807-17,058,414 ECI2-DT, RNU1-11P, 268 more genes
    nsv3921817copy number variation1nstd102humanPathogenic GRCh37 chr6: 2,862,874-16,698,019 , GRCh38 chr6: 2,862,640-16,697,788 , NCBI36 chr6: 2,807,873-16,805,998 RN7SKP293, LOC105374906, 230 more genes
    nsv3920564copy number variation1nstd102humanPathogenic GRCh38 chr6: 3,224,310-30,657,190 , GRCh37 chr6: 3,224,544-30,624,967 , NCBI36 chr6: 3,169,543-30,732,946 PRELID1P2, RPL7AP7, 785 more genes
    nsv3915452copy number variation1nstd102humanLikely pathogenic NCBI36 chr6: 14,838,766-17,662,301 , GRCh37 chr6: 14,730,787-17,554,322 , GRCh38 chr6: 14,730,556-17,554,091 GMPR, JARID2, 32 more genes
    nsv3913920copy number variation1nstd102humanPathogenic GRCh38 chr6: 156,974-46,789,291 , NCBI36 chr6: 101,974-46,864,987 , GRCh37 chr6: 156,974-46,757,028 TRR-ACG1-2, TMEM217, 1385 more genes
    nsv3913657copy number variation1nstd102humanPathogenic NCBI36 chr6: 51,431-18,468,805 , GRCh38 chr6: 106,431-18,360,595 , GRCh37 chr6: 106,431-18,360,826 LOC105374904, CAP2, 294 more genes
    nsv3913192copy number variation1nstd102humanPathogenic NCBI36 chr6: 97,634-15,840,373 , GRCh37.p13 chr6: 152,634-15,732,394 , GRCh38.p12 chr6: 152,634-15,732,163 FARS2, PSMC1P11, 252 more genes
    nsv3913114copy number variation1nstd102humanUncertain significance NCBI36 chr6: 14,900,614-15,532,254 , GRCh37 chr6: 14,792,635-15,424,275 , GRCh38 chr6: 14,792,404-15,424,044 JARID2, JARID2-AS1, 6 more genes
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