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Items: 1 to 20 of 447

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5963603insertion1nstd209human GRCh38 chr7: 93,460,568-93,460,568 , GRCh37.p13 chr7: 93,089,880-93,089,880 CALCR
    nsv5953615insertion1nstd209human GRCh38 chr7: 93,517,298-93,517,298 , GRCh37.p13 chr7: 93,146,610-93,146,610 CALCR
    nsv5950138insertion1nstd209human GRCh38 chr7: 93,532,838-93,532,838 , GRCh37.p13 chr7: 93,162,150-93,162,150 LOC105375400, CALCR
    nsv5926233copy number variation1nstd209human GRCh38 chr7: 93,555,382-93,556,747 , GRCh37.p13 chr7: 93,184,694-93,186,059 CALCR, LOC105375400
    nsv5917459copy number variation1nstd209human GRCh38 chr7: 93,531,551-93,593,896 , GRCh37.p13 chr7: 93,160,863-93,223,208 LOC105375400, CALCR
    nsv5916949copy number variation1nstd209human GRCh38 chr7: 93,526,415-93,526,467 , GRCh37.p13 chr7: 93,155,727-93,155,779 CALCR
    nsv5910891copy number variation1nstd209human GRCh38 chr7: 93,540,675-93,540,790 , GRCh37.p13 chr7: 93,169,987-93,170,102 CALCR, LOC105375400
    nsv5867416copy number variation1nstd209human GRCh38 chr7: 93,541,304-93,546,003 , GRCh37.p13 chr7: 93,170,616-93,175,315 LOC105375400, CALCR
    nsv5862522copy number variation1nstd209human GRCh38 chr7: 93,531,577-93,540,403 , GRCh37.p13 chr7: 93,160,889-93,169,715 LOC105375400, CALCR
    nsv5860016copy number variation2nstd209human GRCh38 chr7: 93,554,973-93,556,796 , GRCh37.p13 chr7: 93,184,285-93,186,108 CALCR, LOC105375400
    nsv5850448copy number variation1nstd209human GRCh38 chr7: 93,546,991-93,593,008 , GRCh37.p13 chr7: 93,176,303-93,222,320 CALCR, LOC105375400
    nsv5729850mobile element insertion2nstd211human GRCh38 chr7: 93,517,315-93,517,315 , GRCh37.p13 chr7: 93,146,627-93,146,627 CALCR
    nsv5727846mobile element insertion1nstd211human GRCh38 chr7: 93,560,083-93,560,083 , GRCh37.p13 chr7: 93,189,395-93,189,395 CALCR
    nsv5682060mobile element insertion1nstd211human GRCh38 chr7: 93,456,817-93,456,817 , GRCh37.p13 chr7: 93,086,129-93,086,129 CALCR
    nsv5678346mobile element insertion1nstd211human GRCh38 chr7: 93,500,589-93,500,589 , GRCh37.p13 chr7: 93,129,901-93,129,901 CALCR
    nsv5637000insertion1nstd207human GRCh38 chr7: 93,460,593-93,460,593 , GRCh37.p13 chr7: 93,089,905-93,089,905 CALCR
    nsv5631181insertion1nstd207human GRCh38 chr7: 93,517,298-93,517,298 , GRCh37.p13 chr7: 93,146,610-93,146,610 CALCR
    nsv5568005copy number variation1nstd207human GRCh38 chr7: 93,540,675-93,540,790 , GRCh37.p13 chr7: 93,169,987-93,170,102 CALCR, LOC105375400
    nsv5557439mobile element insertion1nstd206human GRCh38 chr7: 93,517,298-93,517,298 , GRCh37.p13 chr7: 93,146,610-93,146,610 CALCR
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
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