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Items: 1 to 20 of 113

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5281012copy number variation1nstd204human GRCh38.p13 chr22: 37,662,501-37,724,300 , GRCh37.p13 chr22: 38,058,508-38,120,307 LGALS1, PDXP, 3 more genes
    nsv5160332mobile element insertion1nstd203human GRCh38 chr22: 37,679,107-37,679,205 , GRCh37.p13 chr22: 38,075,114-38,075,212 LGALS1
    nsv5040943copy number variation1nstd200human GRCh38 chr22: 37,662,649-37,682,400 , GRCh37.p13 chr22: 38,058,656-38,078,407 LGALS1, PDXP, 1 more genes
    nsv5037692copy number variation1nstd200human GRCh38 chr22: 37,668,255-37,711,473 , GRCh37.p13 chr22: 38,064,262-38,107,480 LGALS1, TRIOBP, 2 more genes
    nsv5036577copy number variation1nstd200human GRCh38 chr22: 37,671,116-37,675,584 , GRCh37.p13 chr22: 38,067,123-38,071,591 LGALS1
    nsv5031317copy number variation1nstd200human GRCh38 chr22: 37,675,025-37,675,167 , GRCh37.p13 chr22: 38,071,032-38,071,174 LGALS1
    nsv5031043copy number variation1nstd200human GRCh38 chr22: 37,674,302-37,679,189 , GRCh37.p13 chr22: 38,070,309-38,075,196 LGALS1
    nsv4880622copy number variation1nstd200human GRCh37 chr22: 38,064,262-38,107,480 , GRCh38.p12 chr22: 37,668,255-37,711,473 RN7SL385P, TRIOBP, 2 more genes
    nsv4879480copy number variation1nstd200human GRCh37 chr22: 38,067,123-38,071,591 , GRCh38.p12 chr22: 37,671,116-37,675,584 LGALS1
    nsv4729926copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,197,005-51,224,252 , GRCh38.p12 chr22: 16,367,190-50,785,824 FBXO7, GTSE1, 1084 more genes
    nsv4676292copy number variation1nstd102humanPathogenic GRCh37 chr22: 30,654,764-51,197,838 , GRCh38.p12 chr22: 30,258,775-50,759,410 PDXP-DT, PDGFB, 550 more genes
    nsv4676116copy number variation1nstd102humanPathogenic GRCh37 chr22: 38,002,218-38,973,070 , GRCh38.p12 chr22: 37,606,211-38,577,065 CSNK1E, RN7SL704P, 43 more genes
    nsv4670962copy number variation1nstd186human GRCh37 chr22: 38,069,601-38,075,400 , GRCh38.p12 chr22: 37,673,594-37,679,393 LGALS1
    nsv4632242copy number variation1nstd183human GRCh37 chr22: 38,065,863-38,102,890 , GRCh38.p12 chr22: 37,669,856-37,706,883 TRIOBP, LGALS1, 2 more genes
    nsv4628270copy number variation1nstd183human GRCh37 chr22: 38,069,601-38,075,400 , GRCh38.p12 chr22: 37,673,594-37,679,393 LGALS1
    nsv4457771copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,888,899-51,197,838 , GRCh38.p12 chr22: 16,408,173-50,759,410 IGLV3-27, XKR3, 1082 more genes
    nsv4278013copy number variation1nstd166human GRCh37.p13 chr22: 37,381,892-38,500,309 , GRCh38.p12 chr22: 36,985,851-38,104,302 GGA1, GALR3, 46 more genes
    nsv4277060copy number variation1nstd166human GRCh37.p13 chr22: 38,069,607-38,070,322 , GRCh38.p12 chr22: 37,673,600-37,674,315 LGALS1
    nsv4274078copy number variation1nstd166human GRCh37.p13 chr22: 38,067,123-38,071,591 , GRCh38.p12 chr22: 37,671,116-37,675,584 LGALS1
    nsv3922128copy number variation1nstd102humanPathogenic GRCh37 chr22: 35,729,986-39,296,182 , NCBI36 chr22: 34,059,986-37,626,128 , GRCh38 chr22: 35,333,993-38,900,177 LOC102724378, CARD10, 120 more genes
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