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Items: 18

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    Number of Variants: 18

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6290315copy number variation1nstd102humanPathogenic GRCh37 chr20: 42,985,044-48,599,046 , GRCh38.p12 chr20: 44,356,404-49,982,509 ZNFX1, PABPC1L, 170 more genes
    nsv3908507copy number variation1nstd102humanPathogenic GRCh37 chr20: 47,627,844-52,045,480 , GRCh38.p12 chr20: 49,011,307-53,428,941 ZNFX1, LOC100419570, 93 more genes
    nsv3892750copy number variation1nstd102humanPathogenic GRCh37 chr20: 63,244-62,961,294 , GRCh38.p12 chr20: 82,603-64,329,941 ZNFX1, TGIF2-RAB5IF, 1314 more genes
    nsv3905072copy number variation1nstd102humanPathogenic GRCh37 chr20: 63,244-62,948,788 , GRCh38.p12 chr20: 82,603-64,317,435 ZNFX1, LRRN4, 1313 more genes
    nsv3895314copy number variation2nstd102humanPathogenic GRCh37 chr20: 61,569-62,915,555 , GRCh38.p12 chr20: 80,928-64,284,202 ZNFX1, PKIG, 1311 more genes
    nsv3896520copy number variation1nstd102humanPathogenic GRCh37 chr20: 63,244-62,912,463 , GRCh38.p12 chr20: 82,603-64,281,110 ZNFX1, COMMD7, 1311 more genes
    nsv3920218copy number variation1nstd102humanPathogenic GRCh37 chr20: 80,198-62,908,674 , GRCh38 chr20: 99,557-64,277,321 , NCBI36 chr20: 28,198-62,379,118 ZNFX1, MIR3646, 1310 more genes
    nsv3915005copy number variation1nstd102humanPathogenic NCBI36 chr20: 42,849,759-62,379,118 , GRCh37 chr20: 43,416,345-62,908,674 , GRCh38 chr20: 44,787,704-64,277,321 ZNFX1, FTLP1, 472 more genes
    nsv3907741copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 47,726,521-50,427,649 , GRCh38.p12 chr20: 49,109,984-51,811,110 ZNFX1, CEBPB, 70 more genes
    nsv1398389copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 47,682,662-49,884,981 , GRCh38.p12 chr20: 49,066,125-51,268,444 ZNFX1, CEBPB, 65 more genes
    nsv4681865copy number variation1nstd102humanUncertain significance GRCh37 chr20: 47,538,407-48,099,037 , GRCh38.p12 chr20: 48,921,870-49,482,500 ZNFX1, ARFGEF2, 12 more genes
    nsv6112696copy number variation1nstd102humanUncertain significance GRCh38 chr20: 49,212,886-49,410,642 , GRCh37.p13 chr20: 47,829,423-48,027,179 ZNFX1, KCNB1, 7 more genes
    nsv3910818copy number variation1nstd102humanUncertain significance NCBI36 chr20: 25,616,026-62,435,964 , GRCh37.p13 chr20: 25,668,026-62,965,520 , GRCh38.p12 chr20: 25,687,390-64,334,167 ZNFX1, RNA5SP481, 855 more genes
    nsv3874236copy number variation1nstd102humanUncertain significance GRCh37 chr20: 46,962,638-50,647,699 , GRCh38.p12 chr20: 48,333,895-52,031,160 ZNFX1, MIR645, 85 more genes
    nsv6291599copy number variation1nstd102humanUncertain significance GRCh37 chr20: 46,721,299-47,873,110 , GRCh38.p12 chr20: 48,092,556-49,256,573 ZNFX1, PREX1, 16 more genes
    nsv3920108copy number variation1nstd102humanUncertain significance GRCh37 chr20: 47,373,123-48,148,892 , NCBI36 chr20: 46,806,530-47,582,299 , GRCh38 chr20: 48,756,586-49,532,355 ZNFX1, ZFAS1, 14 more genes
    nsv3906682copy number variation1nstd102humanUncertain significance GRCh37 chr20: 47,427,610-48,085,774 , GRCh38.p12 chr20: 48,811,073-49,469,237 ZNFX1, SNAP23P1, 13 more genes
    nsv3922231copy number variation1nstd102humanUncertain significance GRCh38 chr20: 49,098,782-49,465,707 , GRCh37 chr20: 47,715,319-48,082,244 , NCBI36 chr20: 47,148,726-47,515,651 ZNFX1, ZFAS1, 8 more genes
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