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Items: 1 to 20 of 218

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    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
    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
    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
    nsv6133287copy number variation1nstd213human GRCh37 chr16: 88,280,000-90,210,001 , GRCh38.p12 chr16: 88,246,394-90,143,593 AFG3L1P, APRT, 79 more genes
    nsv6133216copy number variation1nstd213human GRCh37 chr16: 88,300,000-89,040,001 , GRCh38.p12 chr16: 88,266,394-88,973,593 APRT, CBFA2T3, 29 more genes
    nsv6133214copy number variation1nstd213human GRCh37 chr16: 85,100,000-90,290,001 , GRCh38.p12 chr16: 85,066,394-90,223,593 AFG3L1P, APRT, 156 more genes
    nsv6133036copy number variation1nstd213human GRCh37 chr16: 85,940,000-90,290,001 , GRCh38.p12 chr16: 85,906,394-90,223,593 AFG3L1P, APRT, 134 more genes
    nsv5287779copy number variation1nstd204human GRCh38.p13 chr16: 88,301,301-89,068,700 , GRCh37.p13 chr16: 88,334,907-89,135,108 , ZFPM1-AS1, 33 more genes
    nsv4729945copy number variation1nstd102humanUncertain significance GRCh37 chr16: 88,222,732-90,155,062 , GRCh38.p12 chr16: 88,189,126-90,088,654 SNORD68, LOC105371412, 75 more genes
    nsv4685754copy number variation1nstd102humannot provided GRCh37 chr16: 61,524,229-90,155,062 , GRCh38.p12 chr16: 61,490,325-90,088,654 LOC100422319, MLYCD, 547 more genes
    nsv4626010copy number variation2nstd183human GRCh37 chr16: 88,705,417-88,830,206 , GRCh38.p12 chr16: 88,639,009-88,763,798 PIEZO1, MIR4722, 9 more genes
    nsv4456065copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,453,448-89,569,215 , GRCh38.p12 chr16: 88,387,040-89,502,807 LOC101927863, LINC00304, 45 more genes
    nsv4455948copy number variation1nstd102humanUncertain significance GRCh37 chr16: 87,848,902-88,809,407 , GRCh38.p12 chr16: 87,815,296-88,742,999 CYBA, BANP, 27 more genes
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