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Items: 1 to 20 of 270

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6637734copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,432,213-30,240,227 , GRCh38.p12 chr16: 29,420,892-30,228,906 SLX1B, LOC606724, 54 more genes
    nsv6637633copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,576,803-30,177,240 , GRCh38.p12 chr16: 21,565,482-30,165,919 USP31, CA5AP1, 200 more genes
    nsv6637500copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,466,731-30,321,320 , GRCh38.p12 chr16: 28,455,410-30,309,999 CA5AP1, NPIPB13, 92 more genes
    nsv6637429copy number variation1nstd102humanPathogenic GRCh37 chr16: 4,380,767-30,445,350 , GRCh38.p12 chr16: 4,330,766-30,434,029 MIR6511B2, ACSM5, 535 more genes
    nsv6623438copy number variation1nstd224human GRCh37 chr16: 29,412,503-29,708,612 , GRCh38.p12 chr16: 29,401,182-29,697,291 CA5AP1, QPRT, 15 more genes
    nsv6623199copy number variation1nstd224human GRCh37 chr16: 29,326,560-29,775,947 , GRCh38.p12 chr16: 29,315,239-29,764,626 LOC388242, SNX29P2, 19 more genes
    nsv6315563copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,432,212-30,177,807 , GRCh38.p12 chr16: 29,420,891-30,166,486 HIRIP3, GDPD3, 45 more genes
    nsv6314862copy number variation1nstd102humanlow penetrance, Likely pathogenic GRCh37.p13 chr16: 29,460,515-30,346,868 , GRCh38 chr16: 29,449,194-30,335,547 ALDOA, CA5AP1, 55 more genes
    nsv6314788copy number variation1nstd220human GRCh37 chr16: 29,410,978-30,305,956 , GRCh38.p12 chr16: 29,399,657-30,294,635 ALDOA, CA5AP1, 56 more genes
    nsv6307590copy number variation1nstd186human GRCh37 chr16: 29,468,321-29,479,807 , GRCh38.p12 chr16: 29,457,000-29,468,486 , SLX1B, 3 more genes
    nsv6307371copy number variation1nstd186human GRCh37 chr16: 29,397,807-29,489,807 , GRCh38.p12 chr16: 29,386,486-29,478,486 , SULT1A4, 8 more genes
    nsv6291754copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,485,883-29,589,674 , GRCh38.p12 chr16: 28,474,562-29,578,353 SULT1A1, CLN3, 44 more genes
    nsv6290312copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 28,353,878-29,478,115 , GRCh38.p12 chr16: 28,342,557-29,466,794 ATP2A1, CD19, 47 more genes
    nsv6290293copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,464,904-30,233,799 , GRCh38.p12 chr16: 29,453,583-30,222,478 QPRT, HIRIP3, 52 more genes
    nsv6290289copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,594,997-29,625,302 , GRCh38.p12 chr16: 21,583,676-29,613,981 LOC105371149, SLX1B, 166 more genes
    nsv6146109copy number variation1nstd206human GRCh38 chr16: 29,386,486-29,478,486 , GRCh37.p13 chr16: 29,397,807-29,489,807 , SULT1A4, 8 more genes
    nsv6145997copy number variation1nstd206human GRCh38 chr16: 29,457,000-29,468,486 , GRCh37.p13 chr16: 29,468,321-29,479,807 , SLX1B, 3 more genes
    nsv6133268copy number variation1nstd213human GRCh37 chr16: 22,710,000-32,010,001 , GRCh38.p12 chr16: 22,698,679-31,998,680 ALDOA, AQP8, 269 more genes
    nsv6133267copy number variation1nstd213human GRCh37 chr16: 22,710,000-30,200,001 , GRCh38.p12 chr16: 22,698,679-30,188,680 ALDOA, AQP8, 169 more genes
    nsv5519942copy number variation1nstd206human GRCh38 chr16: 29,446,486-30,285,000 , GRCh37.p13 chr16: 29,457,807-30,296,321 , CA5AP1, 57 more genes
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