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Items: 1 to 20 of 346

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6129599insertion1nstd186human GRCh37 chr19: 643,120-643,155 , GRCh38.p12 chr19: 643,120-643,155 FGF22
    nsv5973851insertion1nstd209human GRCh38 chr19: 643,104-643,104 , GRCh37.p13 chr19: 643,104-643,104 FGF22
    nsv5936504copy number variation1nstd209human GRCh38 chr19: 642,230-642,315 , GRCh37.p13 chr19: 642,230-642,315 FGF22
    nsv5658881insertion1nstd207human GRCh38 chr19: 642,564-642,564 , GRCh37.p13 chr19: 642,564-642,564 FGF22
    nsv5654362insertion1nstd207human GRCh38 chr19: 643,104-643,104 , GRCh37.p13 chr19: 643,104-643,104 FGF22
    nsv5595427copy number variation1nstd207human GRCh38 chr19: 642,230-642,315 , GRCh37.p13 chr19: 642,230-642,315 FGF22
    nsv5538639insertion1nstd206human GRCh38 chr19: 643,120-643,155 , GRCh37.p13 chr19: 643,120-643,155 FGF22
    nsv5327588copy number variation1nstd204human GRCh38.p13 chr19: 502,284-1,164,314 , GRCh37.p13 chr19: 502,284-1,164,313 RPS2P52, PRSS57, 44 more genes
    nsv5286264copy number variation1nstd204human GRCh37.p13 chr19: 589,909-645,223 , GRCh38.p13 chr19: 589,909-645,223 HCN2, POLRMT, 4 more genes
    nsv5029174copy number variation1nstd200human GRCh38 chr19: 593,541-653,305 , GRCh37.p13 chr19: 593,541-653,305 RNF126, LOC105372234, 4 more genes
    nsv5029164copy number variation1nstd200human GRCh38 chr19: 502,290-1,164,305 , GRCh37.p13 chr19: 502,290-1,164,304 LOC105372235, RNU6-2, 44 more genes
    nsv5018962copy number variation1nstd200human GRCh38 chr19: 642,041-650,310 , GRCh37.p13 chr19: 642,041-650,310 FGF22, RNF126
    nsv4868040copy number variation1nstd200human GRCh37 chr19: 642,041-650,310 , GRCh38.p12 chr19: 642,041-650,310 RNF126, FGF22
    nsv4868038copy number variation1nstd200human GRCh37 chr19: 632,892-641,270 , GRCh38.p12 chr19: 632,892-641,270 POLRMT, LOC105372234, 1 more genes
    nsv4854867copy number variation1nstd200human GRCh37 chr19: 502,290-1,164,304 , GRCh38.p12 chr19: 502,290-1,164,305 LOC100420586, BSG, 44 more genes
    nsv4749286copy number variation1nstd199human GRCh37 chr19: 642,219-642,304 , GRCh38.p12 chr19: 642,219-642,304 FGF22
    nsv4730016copy number variation1nstd102humanLikely benign GRCh37 chr19: 414,714-713,630 , GRCh38.p12 chr19: 414,714-713,630 FSTL3, FGF22, 19 more genes
    nsv4683365copy number variation1nstd102humanUncertain significance GRCh37 chr19: 589,926-1,401,495 , GRCh38.p12 chr19: 589,926-1,401,496 MISP, STK11, 56 more genes
    nsv4676346copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,911-3,501,271 , GRCh38.p12 chr19: 260,911-3,501,273 AZU1, REEP6, 159 more genes
    nsv4676189copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-4,384,674 , GRCh38.p12 chr19: 260,912-4,384,677 MRPL54, DAZAP1, 198 more genes
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