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Items: 1 to 20 of 217

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6734838copy number variation1nstd229human GRCh38 chr3: 150,873,058-150,881,742 , GRCh37.p13 chr3: 150,590,845-150,599,529 MINDY4B
    nsv6729613copy number variation1nstd229human GRCh38 chr3: 150,864,627-150,894,345 , GRCh37.p13 chr3: 150,582,414-150,612,132 MINDY4B
    nsv6728150copy number variation1nstd229human GRCh38 chr3: 150,865,901-150,871,300 , GRCh37.p13 chr3: 150,583,688-150,589,087 MINDY4B
    nsv6726612copy number variation1nstd229human GRCh38 chr3: 150,832,132-151,163,131 , GRCh37.p13 chr3: 150,549,919-150,880,918 MINDY4B, MED12L, 2 more genes
    nsv6718687copy number variation1nstd229human GRCh38 chr3: 150,888,393-150,888,423 , GRCh37.p13 chr3: 150,606,180-150,606,210 MINDY4B
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 H1-10, AADACL2-AS1, 846 more genes
    nsv6636766copy number variation1nstd102humanUncertain significance GRCh37 chr3: 150,546,825-150,878,912 , GRCh38.p12 chr3: 150,829,038-151,161,125 MINDY4B, MED12L, 2 more genes
    nsv6636735copy number variation1nstd102humanUncertain significance GRCh37 chr3: 150,534,296-150,908,849 , GRCh38.p12 chr3: 150,816,509-151,191,062 MINDY4B, MED12L, 3 more genes
    nsv6628653copy number variation1nstd224human GRCh37 chr3: 150,541,363-150,873,241 , GRCh38.p12 chr3: 150,823,576-151,155,454 MINDY4B, CLRN1, 2 more genes
    nsv6557524inversion1nstd223human GRCh38 chr3: 150,868,216-150,869,015 , GRCh37.p13 chr3: 150,586,003-150,586,802 MINDY4B
    nsv6313678copy number variation1nstd102humanPathogenic GRCh37 chr3: 145,486,960-160,504,834 , GRCh38.p12 chr3: 145,769,173-160,787,046 RNU6-901P, RPL32P8, 229 more genes
    nsv6311444copy number variation1nstd102humanPathogenic GRCh37 chr3: 148,447,967-151,176,497 , GRCh38.p12 chr3: 148,730,180-151,458,709 TM4SF1, FKBP1AP4, 68 more genes
    nsv6290273copy number variation1nstd102humanPathogenic GRCh37 chr3: 142,729,607-157,921,084 , GRCh38.p12 chr3: 143,010,765-158,203,295 LINC02066, TM4SF1-AS1, 206 more genes
    nsv6290244copy number variation1nstd102humanPathogenic GRCh37 chr3: 143,439,359-165,252,122 , GRCh38.p12 chr3: 143,720,517-165,534,334 LOC102724145, C3orf80, 273 more genes
    nsv6134674copy number variation1nstd213human GRCh37 chr3: 150,600,000-153,170,001 , GRCh38.p12 chr3: 150,882,213-153,452,212 CLRN1-AS1, MBNL1-AS1, 37 more genes
    nsv5904566copy number variation1nstd209human GRCh38 chr3: 150,869,196-150,869,516 , GRCh37.p13 chr3: 150,586,983-150,587,303 MINDY4B
    nsv5898151copy number variation1nstd209human GRCh38 chr3: 150,871,250-150,878,335 , GRCh37.p13 chr3: 150,589,037-150,596,122 MINDY4B
    nsv5892126copy number variation1nstd209human GRCh38 chr3: 150,871,379-150,871,449 , GRCh37.p13 chr3: 150,589,166-150,589,236 MINDY4B
    nsv5834366copy number variation1nstd209human GRCh38 chr3: 150,871,183-150,877,831 , GRCh37.p13 chr3: 150,588,970-150,595,618 MINDY4B
    nsv5687154mobile element insertion1nstd211human GRCh38 chr3: 150,881,633-150,881,633 , GRCh37.p13 chr3: 150,599,420-150,599,420 MINDY4B
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