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Items: 1 to 20 of 662

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148130copy number variation1nstd102humanPathogenic GRCh37 chr8: 36,763,176-50,929,707 , GRCh38.p12 chr8: 36,905,658-50,017,147 SNTG1, RN7SL806P, 193 more genes
    nsv7097904copy number variation1nstd102humanPathogenic GRCh37 chr8: 41,525,765-41,526,102 , GRCh38.p12 chr8: 41,668,247-41,668,584 ANK1
    nsv7097903copy number variation1nstd102humanUncertain significance GRCh37 chr8: 41,518,984-42,698,237 , GRCh38.p12 chr8: 41,661,466-42,843,094 DKK4, KAT6A, 22 more genes
    nsv7097794copy number variation1nstd102humanPathogenic GRCh37 chr8: 41,542,042-41,615,675 , GRCh38.p12 chr8: 41,684,524-41,758,157 ANK1
    nsv7097662copy number variation2nstd102humanUncertain significance GRCh37 chr8: 41,518,984-43,054,712 , GRCh38.p12 chr8: 41,661,466-43,199,569 LOC101059972, IKBKB-DT, 31 more genes
    nsv7065639inversion1nstd229human GRCh38 chr8: 40,079,981-42,715,940 , GRCh37.p13 chr8: 39,937,500-42,571,083 LOC105379390, RPL17P30, 44 more genes
    nsv7062022inversion1nstd229human GRCh38 chr8: 41,644,817-41,655,175 , GRCh37.p13 chr8: 41,502,336-41,512,694 ANK1, NKX6-3
    nsv6857641copy number variation1nstd229human GRCh38 chr8: 41,760,280-41,764,248 , GRCh37.p13 chr8: 41,617,798-41,621,766 ANK1
    nsv6857084copy number variation1nstd229human GRCh38 chr8: 41,769,863-41,773,350 , GRCh37.p13 chr8: 41,627,381-41,630,868 ANK1
    nsv6855686copy number variation1nstd229human GRCh38 chr8: 41,878,484-41,887,908 , GRCh37.p13 chr8: 41,736,002-41,745,426 ANK1
    nsv6855592copy number variation1nstd229human GRCh38 chr8: 41,790,969-41,793,437 , GRCh37.p13 chr8: 41,648,487-41,650,955 ANK1
    nsv6855513copy number variation1nstd229human GRCh38 chr8: 41,653,792-41,654,318 , GRCh37.p13 chr8: 41,511,311-41,511,837 ANK1
    nsv6854754copy number variation1nstd229human GRCh38 chr8: 41,751,964-41,782,091 , GRCh37.p13 chr8: 41,609,482-41,639,609 ANK1
    nsv6854372copy number variation1nstd229human GRCh38 chr8: 41,805,065-41,810,634 , GRCh37.p13 chr8: 41,662,583-41,668,152 ANK1
    nsv6854250copy number variation1nstd229human GRCh38 chr8: 41,703,901-41,706,800 , GRCh37.p13 chr8: 41,561,419-41,564,318 ANK1
    nsv6853728copy number variation1nstd229human GRCh38 chr8: 41,849,309-41,855,058 , GRCh37.p13 chr8: 41,706,827-41,712,576 ANK1
    nsv6853579copy number variation1nstd229human GRCh38 chr8: 41,743,310-41,743,603 , GRCh37.p13 chr8: 41,600,828-41,601,121 ANK1
    nsv6852660copy number variation1nstd229human GRCh38 chr8: 41,803,785-41,803,818 , GRCh37.p13 chr8: 41,661,303-41,661,336 ANK1
    nsv6852035copy number variation1nstd229human GRCh38 chr8: 41,602,240-41,710,755 , GRCh37.p13 chr8: 41,459,759-41,568,273 NKX6-3, ANK1, 3 more genes
    nsv6851983copy number variation1nstd229human GRCh38 chr8: 41,823,539-41,824,884 , GRCh37.p13 chr8: 41,681,057-41,682,402 ANK1
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