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Items: 1 to 20 of 148

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7039296inversion1nstd229human GRCh38 chr4: 67,387,981-67,451,854 , GRCh37.p13 chr4: 68,253,699-68,317,572 RNU1-63P, LOC101927237, 1 more genes
    nsv7039205inversion1nstd229human GRCh38 chr4: 67,421,462-67,433,897 , GRCh37.p13 chr4: 68,287,180-68,299,615 LOC101927237, RNU1-63P
    nsv6755378copy number variation1nstd229human GRCh38 chr4: 67,421,967-67,432,511 , GRCh37.p13 chr4: 68,287,685-68,298,229 RNU1-63P, LOC101927237
    nsv6751578copy number variation1nstd229human GRCh38 chr4: 67,017,904-67,499,142 , GRCh37.p13 chr4: 67,883,622-68,364,860 RNA5SP527, CENPC, 3 more genes
    nsv6750142copy number variation1nstd229human GRCh38 chr4: 67,412,001-67,416,700 , GRCh37.p13 chr4: 68,277,719-68,282,418 LOC101927237
    nsv6741348copy number variation1nstd229human GRCh38 chr4: 67,374,723-67,478,419 , GRCh37.p13 chr4: 68,240,441-68,344,137 CENPC, RNA5SP527, 2 more genes
    nsv6738666copy number variation1nstd229human GRCh38 chr4: 66,318,664-67,575,458 , GRCh37.p13 chr4: 67,184,382-68,441,176 STAP1, RNU6-699P, 6 more genes
    nsv6637038copy number variation1nstd102humanUncertain significance GRCh37 chr4: 67,729,321-68,949,586 , GRCh38.p12 chr4: 66,863,603-68,083,868 UBA6-DT, LOC101927237, 24 more genes
    nsv6636883copy number variation1nstd102humanUncertain significance GRCh37 chr4: 66,215,872-68,647,080 , GRCh38.p12 chr4: 65,350,154-67,781,362 LOC100419046, LOC105377260, 24 more genes
    nsv6391804copy number variation1nstd223human GRCh38 chr4: 67,415,404-67,433,822 , GRCh37.p13 chr4: 68,281,122-68,299,540 RNU1-63P, LOC101927237
    nsv6389239copy number variation1nstd223human GRCh38 chr4: 67,374,701-67,478,600 , GRCh37.p13 chr4: 68,240,419-68,344,318 LOC101927237, RNA5SP527, 2 more genes
    nsv6388036copy number variation1nstd223human GRCh38 chr4: 67,352,729-67,439,106 , GRCh37.p13 chr4: 68,218,447-68,304,824 RNU1-63P, RNA5SP527, 1 more genes
    nsv6313845copy number variation1nstd102humanUncertain significance GRCh37 chr4: 68,272,006-68,923,410 , GRCh38.p12 chr4: 67,406,288-68,057,692 TMPRSS11F, TMPRSS11D, 20 more genes
    nsv6313740copy number variation1nstd102humanPathogenic GRCh37 chr4: 61,867,555-74,711,517 , GRCh38.p12 chr4: 61,001,837-73,845,800 CXCL8, UGT2A1, 175 more genes
    nsv6291432copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354 SNHG27, TNIP3, 1091 more genes
    nsv6135600copy number variation1nstd213human GRCh37 chr4: 68,260,000-69,150,001 , GRCh38.p12 chr4: 67,394,282-68,284,283 TMPRSS11B, TMPRSS11BNL, 25 more genes
    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
    nsv5472277copy number variation1nstd206human GRCh38 chr4: 67,374,723-67,478,420 , GRCh37.p13 chr4: 68,240,441-68,344,138 RNU1-63P, CENPC, 2 more genes
    nsv5460832copy number variation1nstd206human GRCh38 chr4: 67,415,404-67,433,823 , GRCh37.p13 chr4: 68,281,122-68,299,541 RNU1-63P, LOC101927237
    nsv5084120mobile element insertion1nstd203human GRCh38 chr4: 67,418,743-67,418,759 , GRCh37.p13 chr4: 68,284,461-68,284,477 LOC101927237
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