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Items: 1 to 20 of 119

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5960886insertion1nstd209human GRCh38 chr6: 159,898,616-159,898,616 , GRCh37.p13 chr6: 160,319,648-160,319,648 MAS1
    nsv5906619copy number variation1nstd209human GRCh38 chr6: 159,906,702-159,910,486 , GRCh37.p13 chr6: 160,327,734-160,331,518 MAS1
    nsv5895916copy number variation1nstd209human GRCh38 chr6: 159,905,780-159,913,100 , GRCh37.p13 chr6: 160,326,812-160,334,132 MAS1
    nsv5844774copy number variation2nstd209human GRCh38 chr6: 159,907,987-159,911,222 , GRCh37.p13 chr6: 160,329,019-160,332,254 MAS1
    nsv5844687copy number variation2nstd209human GRCh38 chr6: 159,909,023-159,910,647 , GRCh37.p13 chr6: 160,330,055-160,331,679 MAS1
    nsv5844152copy number variation1nstd209human GRCh38 chr6: 159,906,837-159,908,336 , GRCh37.p13 chr6: 160,327,869-160,329,368 MAS1
    nsv5638344insertion1nstd207human GRCh38 chr6: 159,898,616-159,898,616 , GRCh37.p13 chr6: 160,319,648-160,319,648 MAS1
    nsv5310684copy number variation1nstd204human GRCh38.p13 chr6: 159,734,848-159,969,288 , GRCh37.p13 chr6: 160,155,880-160,390,320 SNORA29, SOD2-OT1, 9 more genes
    nsv5221863copy number variation1nstd204human GRCh38.p13 chr6: 159,734,701-159,927,700 , GRCh37.p13 chr6: 160,155,733-160,348,732 PNLDC1, SNORA20, 8 more genes
    nsv4824839copy number variation1nstd200human GRCh37 chr6: 160,155,890-160,390,316 , GRCh38.p12 chr6: 159,734,858-159,969,284 SNORA29, MRPL18, 9 more genes
    nsv4817812copy number variation1nstd200human GRCh37 chr6: 160,327,738-160,331,519 , GRCh38.p12 chr6: 159,906,706-159,910,487 MAS1
    nsv4766814inversion1nstd199human GRCh37 chr6: 153,752,140-161,206,728 , GRCh38.p12 chr6: 153,431,005-160,785,696 , ACAT2, 111 more genes
    nsv4729113copy number variation1nstd102humanUncertain significance GRCh37 chr6: 159,998,877-160,413,982 , GRCh38.p12 chr6: 159,577,845-159,992,950 PNLDC1, MRPL18, 12 more genes
    nsv4455446copy number variation1nstd102humanUncertain significance GRCh37 chr6: 157,262,571-160,992,289 , GRCh38.p12 chr6: 156,941,437-160,571,257 LOC105378076, LOC107986663, 67 more genes
    nsv4442247insertion1nstd175human GRCh37 chr6: 160,319,648-160,319,648 , GRCh38.p12 chr6: 159,898,616-159,898,616 MAS1
    nsv4436131complex substitution1nstd102humanPathogenic GRCh38.p12 chr6: 151,122,197-170,745,979 , GRCh37 chr6: 151,443,333-171,115,067 ACAT2, CCR6, 303 more genes
    nsv4374103copy number variation1nstd173human GRCh37 chr6: 160,313,399-160,453,690 , GRCh38.p12 chr6: 159,892,367-160,032,658 MAS1, IGF2R, 1 more genes
    nsv4372759copy number variation1nstd173human GRCh37 chr6: 160,315,586-160,453,690 , GRCh38.p12 chr6: 159,894,554-160,032,658 MAS1, IGF2R, 1 more genes
    nsv4330897inversion1nstd166human GRCh37.p13 chr6: 90,629,263-160,387,383 , GRCh38.p12 chr6: 89,919,544-159,966,351 , ACAT2, 894 more genes
    nsv3948259insertion1nstd167human GRCh37 chr6: 160,319,648-160,319,648 , GRCh38.p12 chr6: 159,898,616-159,898,616 MAS1
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