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Items: 1 to 20 of 384

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096197copy number variation1nstd102humanPathogenic GRCh37 chr2: 127,806,102-129,076,137 , GRCh38.p12 chr2: 127,048,526-128,318,563 IWS1, ZFP91P1, 35 more genes
    nsv7095853copy number variation1nstd102humanPathogenic GRCh37 chr2: 127,451,420-129,076,137 , GRCh38.p12 chr2: 126,693,844-128,318,563 SRMP3, DYNLT3P2, 41 more genes
    nsv7056053inversion1nstd229human GRCh38 chr2: 127,478,636-127,828,579 , GRCh37.p13 chr2: 128,236,212-128,586,153 MYO7B, IWS1, 7 more genes
    nsv7055804inversion1nstd229human GRCh38 chr2: 127,449,381-127,615,368 , GRCh37.p13 chr2: 128,206,957-128,372,943 RNU4-48P, IWS1, 3 more genes
    nsv7051453inversion1nstd229human GRCh38 chr2: 127,202,996-128,332,828 , GRCh37.p13 chr2: 127,960,572-129,090,402 WDR33, RNU4-48P, 32 more genes
    nsv7043911inversion1nstd229human GRCh38 chr2: 127,560,469-127,828,747 , GRCh37.p13 chr2: 128,318,044-128,586,321 LIMS2, SFT2D3, 6 more genes
    nsv7040291inversion1nstd229human GRCh38 chr2: 127,202,908-127,840,585 , GRCh37.p13 chr2: 127,960,484-128,598,159 LIMS2, LOC101927834, 18 more genes
    nsv7039545inversion1nstd229human GRCh38 chr2: 127,588,395-127,588,541 , GRCh37.p13 chr2: 128,345,970-128,346,116 MYO7B
    nsv7038180inversion1nstd229human GRCh38 chr2: 127,592,383-127,592,398 , GRCh37.p13 chr2: 128,349,958-128,349,973 MYO7B
    nsv6697324copy number variation1nstd229human GRCh38 chr2: 127,637,217-127,637,254 , GRCh37.p13 chr2: 128,394,792-128,394,829 LIMS2, MYO7B
    nsv6696578copy number variation1nstd229human GRCh38 chr2: 127,603,740-127,607,634 , GRCh37.p13 chr2: 128,361,315-128,365,209 MYO7B
    nsv6694380copy number variation1nstd229human GRCh38 chr2: 127,571,819-127,580,422 , GRCh37.p13 chr2: 128,329,394-128,337,997 MYO7B
    nsv6693424copy number variation1nstd229human GRCh38 chr2: 127,624,078-127,626,474 , GRCh37.p13 chr2: 128,381,653-128,384,049 MYO7B, LOC101927834
    nsv6692218copy number variation1nstd229human GRCh38 chr2: 127,547,351-127,551,110 , GRCh37.p13 chr2: 128,304,926-128,308,685 MYO7B
    nsv6692145copy number variation1nstd229human GRCh38 chr2: 127,546,308-127,550,513 , GRCh37.p13 chr2: 128,303,883-128,308,088 MYO7B
    nsv6692054copy number variation1nstd229human GRCh38 chr2: 127,579,043-127,581,613 , GRCh37.p13 chr2: 128,336,618-128,339,188 MYO7B
    nsv6690376copy number variation1nstd229human GRCh38 chr2: 127,634,700-127,634,744 , GRCh37.p13 chr2: 128,392,275-128,392,319 MYO7B
    nsv6689933copy number variation1nstd229human GRCh38 chr2: 127,414,334-127,642,627 , GRCh37.p13 chr2: 128,171,910-128,400,202 LIMS2, LOC101927834, 7 more genes
    nsv6689318copy number variation1nstd229human GRCh38 chr2: 127,423,001-127,702,100 , GRCh37.p13 chr2: 128,180,577-128,459,674 LOC101927834, MIR4783, 10 more genes
    nsv6688828copy number variation1nstd229human GRCh38 chr2: 127,436,502-128,393,799 , GRCh37.p13 chr2: 128,194,078-129,151,373 LOC107985944, LOC105373610, 25 more genes
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