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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv1398432copy number variation1nstd102humanPathogenic GRCh37 chr22: 35,680,095-38,098,981 , GRCh38.p12 chr22: 35,284,102-37,702,974 MTCO1P20, APOL3, 74 more genes
    nsv1395496copy number variation1nstd122human NCBI36 chr22: 36,384,405-36,402,938 , GRCh37.p13 chr22: 38,054,459-38,072,992 , GRCh38.p12 chr22: 37,658,452-37,676,985 RN7SL385P, PDXP, 2 more genes
    nsv1394171copy number variation1nstd122human NCBI36 chr22: 36,384,405-36,385,007 , GRCh37.p13 chr22: 38,054,459-38,055,061 , GRCh38.p12 chr22: 37,658,452-37,659,054 PDXP-DT, PDXP
    nsv1392913copy number variation6nstd122human NCBI36 chr22: 36,384,661-36,385,007 , GRCh37.p13 chr22: 38,054,715-38,055,061 , GRCh38.p12 chr22: 37,658,708-37,659,054 PDXP, PDXP-DT
    nsv1391286copy number variation2nstd122human NCBI36 chr22: 36,384,610-36,385,007 , GRCh37.p13 chr22: 38,054,664-38,055,061 , GRCh38.p12 chr22: 37,658,657-37,659,054 PDXP, PDXP-DT
    nsv1190106copy number variation1nstd113human NCBI36 chr22: 35,774,273-37,032,224 , GRCh37.p13 chr22: 37,444,327-38,702,278 , GRCh38.p12 chr22: 37,048,287-38,306,273 SOX10, SSTR3, 49 more genes
    nsv1142581copy number variation1nstd106human GRCh37 chr22: 32,699,561-44,636,874 , GRCh38.p12 chr22: 32,303,574-44,240,994 , PRDX3P1, 345 more genes
    esv3815798copy number variation1estd192human GRCh37 chr22: 23,611,266-39,769,406 , GRCh38.p12 chr22: 23,269,079-39,373,401 , LARGE1, 446 more genes
    esv3796963inversion1estd192human GRCh37 chr22: 36,502,677-43,391,318 , GRCh38.p12 chr22: 36,106,629-42,995,312 , TPTEP2, 258 more genes
    esv3807866copy number variation1estd192human GRCh37 chr22: 36,748,507-39,136,874 , GRCh38.p12 chr22: 36,352,462-38,740,869 , TPTEP2-CSNK1E, 91 more genes
    esv3814597inversion1estd192human GRCh37 chr22: 17,581,515-42,468,183 , GRCh38.p12 chr22: 17,100,625-42,072,179 , IGLV3-2, 868 more genes
    esv3800256copy number variation1estd192human GRCh37 chr22: 26,403,935-49,444,943 , GRCh38.p12 chr22: 26,007,969-49,049,131 , RPL6P28, 610 more genes
    esv3802173copy number variation1estd192human GRCh37 chr22: 27,743,368-41,337,372 , GRCh38.p12 chr22: 27,347,407-40,941,368 , MTCYBP34, 366 more genes
    esv3803398tandem duplication1estd192human GRCh37 chr22: 37,699,353-46,579,844 , GRCh38.p12 chr22: 37,303,312-46,183,947 , LINC01589, 300 more genes
    esv3809019copy number variation1estd192human GRCh37 chr22: 22,082,709-43,415,957 , GRCh38.p12 chr22: 21,728,420-43,019,951 , BCR, 712 more genes
    esv3785901copy number variation1estd192human GRCh37 chr22: 31,945,359-48,634,713 , GRCh38.p12 chr22: 31,549,373-48,238,901 , LOC100506472, 448 more genes
    esv3787499tandem duplication1estd192human GRCh37 chr22: 36,298,831-38,654,431 , GRCh38.p12 chr22: 35,902,783-38,258,425 , APOL4, 86 more genes
    esv3784911tandem duplication1estd192human GRCh37 chr22: 37,856,276-38,755,639 , GRCh38.p12 chr22: 37,460,238-38,359,634 PICK1, GALR3, 37 more genes
    esv3778633copy number variation1estd192human GRCh37 chr22: 25,941,249-40,884,349 , GRCh38.p12 chr22: 25,545,282-40,488,345 , FAM83F, 391 more genes
    esv3789996tandem duplication1estd192human GRCh37 chr22: 37,944,666-43,562,131 , GRCh38.p12 chr22: 37,548,659-43,166,125 , GRAP2, 212 more genes
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