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Items: 1 to 20 of 201

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7055490inversion1nstd229human GRCh38 chr6: 25,672,047-25,672,704 , GRCh37.p13 chr6: 25,672,275-25,672,932 SCGN
    nsv7048539inversion1nstd229human GRCh38 chr6: 25,696,324-25,696,461 , GRCh37.p13 chr6: 25,696,552-25,696,689 SCGN
    nsv6793281copy number variation1nstd229human GRCh38 chr6: 25,659,789-25,661,458 , GRCh37.p13 chr6: 25,660,017-25,661,686 SCGN
    nsv6790394copy number variation1nstd229human GRCh38 chr6: 25,701,984-25,702,712 , GRCh37.p13 chr6: 25,702,212-25,702,940 SCGN
    nsv6788157copy number variation1nstd229human GRCh38 chr6: 25,668,311-25,672,892 , GRCh37.p13 chr6: 25,668,539-25,673,120 SCGN
    nsv6787290copy number variation1nstd229human GRCh38 chr6: 25,240,953-26,330,257 , GRCh37.p13 chr6: 25,241,181-26,330,485 CARMIL1, H2AC8, 74 more genes
    nsv6785917copy number variation1nstd229human GRCh38 chr6: 25,619,649-25,744,363 , GRCh37.p13 chr6: 25,619,877-25,744,591 H2BC1, PRELID1P2, 6 more genes
    nsv6783968copy number variation1nstd229human GRCh38 chr6: 25,284,234-25,728,953 , GRCh37.p13 chr6: 25,284,462-25,729,181 RNU6-987P, H2BC1, 5 more genes
    nsv6783569copy number variation1nstd229human GRCh38 chr6: 25,647,222-25,651,095 , GRCh37.p13 chr6: 25,647,450-25,651,323 SCGN
    nsv6781730copy number variation1nstd229human GRCh38 chr6: 25,647,220-25,651,095 , GRCh37.p13 chr6: 25,647,448-25,651,323 SCGN
    nsv6403623copy number variation1nstd223human GRCh38 chr6: 25,668,310-25,672,891 , GRCh37.p13 chr6: 25,668,538-25,673,119 SCGN
    nsv6402318copy number variation1nstd223human GRCh38 chr6: 25,240,953-26,330,257 , GRCh37.p13 chr6: 25,241,181-26,330,485 H2BC7, H2AC7, 74 more genes
    nsv6304116copy number variation1nstd186human GRCh37 chr6: 25,643,539-25,650,617 , GRCh38.p12 chr6: 25,643,311-25,650,389 SCGN
    nsv6302950copy number variation1nstd186human GRCh37 chr6: 25,647,193-25,651,323 , GRCh38.p12 chr6: 25,646,965-25,651,095 SCGN
    nsv6011957copy number variation1nstd212human GRCh38 chr6: 25,658,003-25,658,054 , GRCh37.p13 chr6: 25,658,231-25,658,282 SCGN
    nsv5949113insertion1nstd209human GRCh38 chr6: 25,671,812-25,671,812 , GRCh37.p13 chr6: 25,672,040-25,672,040 SCGN
    nsv5903780copy number variation1nstd209human GRCh38 chr6: 25,647,220-25,651,094 , GRCh37.p13 chr6: 25,647,448-25,651,322 SCGN
    nsv5888091copy number variation1nstd209human GRCh38 chr6: 25,641,998-25,652,127 , GRCh37.p13 chr6: 25,642,226-25,652,355 SCGN
    nsv5844844copy number variation1nstd209human GRCh38 chr6: 25,642,833-25,651,062 , GRCh37.p13 chr6: 25,643,061-25,651,290 SCGN
    nsv5680252mobile element insertion2nstd211human GRCh38 chr6: 25,671,830-25,671,830 , GRCh37.p13 chr6: 25,672,058-25,672,058 SCGN
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