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Items: 1 to 20 of 292

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147840insertion1nstd232human GRCh37.p13 chr16: 88,712,712-88,712,712 , GRCh38.p12 chr16: 88,646,304-88,646,304 CYBA
    nsv7094699copy number variation2nstd102humanUncertain significance GRCh37 chr16: 87,636,753-90,109,753 , GRCh38.p12 chr16: 87,603,147-90,043,345 HSALR1, LOC105371412, 87 more genes
    nsv7076684inversion1nstd229human GRCh38 chr16: 88,596,668-89,175,422 , GRCh37.p13 chr16: 88,663,076-89,241,830 LOC102724632, MIR4722, 28 more genes
    nsv6992726copy number variation1nstd229human GRCh38 chr16: 88,648,114-88,650,955 , GRCh37.p13 chr16: 88,714,522-88,717,363 MVD, CYBA
    nsv6992445copy number variation1nstd229human GRCh38 chr16: 88,646,967-88,734,164 , GRCh37.p13 chr16: 88,713,375-88,800,572 RNF166, SNAI3, 7 more genes
    nsv6979703copy number variation1nstd229human GRCh38 chr16: 88,192,059-88,802,307 , GRCh37.p13 chr16: 88,225,665-88,868,715 SNAI3, SNAI3-AS1, 20 more genes
    nsv6637701copy number variation1nstd102humanUncertain significance GRCh37 chr16: 88,697,181-88,809,407 , GRCh38.p12 chr16: 88,630,773-88,742,999 MVD, RNF166, 10 more genes
    nsv6634465copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 71,610,276-90,354,753 , GRCh38.p12 chr16: 71,576,373-90,228,345 AP1G1, AFG3L1P, 349 more genes
    nsv6624182copy number variation1nstd224human GRCh37 chr16: 88,358,766-89,261,442 , GRCh38.p12 chr16: 88,325,160-89,195,034 CDH15, CDT1, 36 more genes
    nsv6505258copy number variation1nstd223human GRCh38 chr16: 88,641,479-88,641,920 , GRCh37.p13 chr16: 88,707,887-88,708,328 CYBA
    nsv6504646copy number variation1nstd223human GRCh38 chr16: 88,643,958-88,644,651 , GRCh37.p13 chr16: 88,710,366-88,711,059 CYBA
    nsv6497666copy number variation1nstd223human GRCh38 chr16: 88,648,761-88,649,082 , GRCh37.p13 chr16: 88,715,169-88,715,490 CYBA
    nsv6315145copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,365,786-89,584,412 , GRCh38.p12 chr16: 88,332,180-89,518,004 SPG7, PABPN1L, 46 more genes
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 ATMIN, ATP6V0D1, 826 more genes
    nsv6310102copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,717,354-88,718,353 , GRCh38.p12 chr16: 88,650,946-88,651,945 MVD, CYBA
    nsv6310023copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,713,499-88,718,353 , GRCh38.p12 chr16: 88,647,091-88,651,945 MVD, CYBA
    nsv6310022copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,712,514-88,718,096 , GRCh38.p12 chr16: 88,646,106-88,651,688 MVD, CYBA
    nsv6291569copy number variation1nstd102humanUncertain significance GRCh37 chr16: 88,000,389-90,155,062 , GRCh38.p12 chr16: 87,966,783-90,088,654 CTU2, CDT1, 78 more genes
    nsv6290331copy number variation1nstd102humanPathogenic GRCh37 chr16: 80,386,595-90,163,348 , GRCh38.p12 chr16: 80,352,698-90,096,940 GINS2, TCF25, 220 more genes
    nsv6286803insertion1nstd214human GRCh38 chr16: 88,646,331-88,646,331 , GRCh37.p13 chr16: 88,712,739-88,712,739 CYBA
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