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Items: 1 to 20 of 320

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5957298insertion1nstd209human GRCh38 chr4: 73,267,220-73,267,220 , GRCh37.p13 chr4: 74,132,937-74,132,937 ANKRD17-DT
    nsv5951425insertion1nstd209human GRCh38 chr4: 73,270,285-73,270,285 , GRCh37.p13 chr4: 74,136,002-74,136,002 ANKRD17-DT
    nsv5903330copy number variation1nstd209human GRCh38 chr4: 73,287,094-73,297,652 , GRCh37.p13 chr4: 74,152,811-74,163,369 ANKRD17-DT
    nsv5893576copy number variation1nstd209human GRCh38 chr4: 67,920,462-75,134,545 , GRCh37.p13 chr4: 68,786,180-76,059,755 , DCK, 147 more genes
    nsv5840375copy number variation1nstd209human GRCh38 chr4: 73,287,066-73,297,750 , GRCh37.p13 chr4: 74,152,783-74,163,467 ANKRD17-DT
    nsv5839788copy number variation1nstd209human GRCh38 chr4: 73,357,636-73,360,045 , GRCh37.p13 chr4: 74,223,353-74,225,762 ANKRD17-DT
    nsv5730920mobile element insertion1nstd211human GRCh38 chr4: 73,345,830-73,345,830 , GRCh37.p13 chr4: 74,211,547-74,211,547 ANKRD17-DT
    nsv5730257mobile element insertion1nstd211human GRCh38 chr4: 73,304,184-73,304,184 , GRCh37.p13 chr4: 74,169,901-74,169,901 ANKRD17-DT
    nsv5724326mobile element insertion1nstd211human GRCh38 chr4: 73,302,385-73,302,385 , GRCh37.p13 chr4: 74,168,102-74,168,102 ANKRD17-DT
    nsv5694110mobile element insertion1nstd211human GRCh38 chr4: 73,277,044-73,277,044 , GRCh37.p13 chr4: 74,142,761-74,142,761 ANKRD17-DT
    nsv5691009mobile element insertion2nstd211human GRCh38 chr4: 73,268,071-73,268,071 , GRCh37.p13 chr4: 74,133,788-74,133,788 ANKRD17-DT
    nsv5685888mobile element insertion2nstd211human GRCh38 chr4: 73,326,396-73,326,396 , GRCh37.p13 chr4: 74,192,113-74,192,113 ANKRD17-DT
    nsv5674237copy number variation1nstd102humanPathogenic GRCh38 chr4: 51,891,814-76,009,719 , GRCh37.p13 chr4: 52,757,980-76,930,872 FTLP10, RNU6-410P, 335 more genes
    nsv5614466insertion1nstd207human GRCh38 chr4: 73,267,220-73,267,220 , GRCh37.p13 chr4: 74,132,937-74,132,937 ANKRD17-DT
    nsv5557869mobile element insertion1nstd206human GRCh38 chr4: 73,345,830-73,345,881 , GRCh37.p13 chr4: 74,211,547-74,211,598 ANKRD17-DT
    nsv5551849insertion1nstd206human GRCh38 chr4: 73,326,396-73,326,401 , GRCh37.p13 chr4: 74,192,113-74,192,118 ANKRD17-DT
    nsv5547030insertion1nstd206human GRCh38 chr4: 68,996,170-113,894,177 , GRCh37.p13 chr4: 69,861,888-114,815,333 , MIR548AH, 616 more genes
    nsv5543501insertion1nstd206human GRCh38 chr4: 73,267,220-73,267,220 , GRCh37.p13 chr4: 74,132,937-74,132,937 ANKRD17-DT
    nsv5472236copy number variation1nstd206human GRCh38 chr4: 73,274,845-73,274,923 , GRCh37.p13 chr4: 74,140,562-74,140,640 ANKRD17-DT
    nsv5472101copy number variation1nstd206human GRCh38 chr4: 73,287,097-73,297,653 , GRCh37.p13 chr4: 74,152,814-74,163,370 ANKRD17-DT
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