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Items: 1 to 20 of 189

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094940copy number variation1nstd102humanUncertain significance GRCh37 chr16: 89,611,036-90,106,937 , GRCh38.p12 chr16: 89,544,628-90,040,529 SPATA2L, LINC02166, 25 more genes
    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
    nsv7066481inversion1nstd229human GRCh38 chr16: 89,970,591-89,992,088 , GRCh37.p13 chr16: 90,036,999-90,058,496 AFG3L1P, CENPBD1P
    nsv6989345copy number variation1nstd229human GRCh38 chr16: 89,973,198-89,999,772 , GRCh37.p13 chr16: 90,039,606-90,066,180 CENPBD1P, AFG3L1P
    nsv6988645copy number variation1nstd229human GRCh38 chr16: 89,954,762-90,000,112 , GRCh37.p13 chr16: 90,021,170-90,066,520 DEF8, CENPBD1P, 1 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
    nsv6512450copy number variation1nstd223human GRCh38 chr16: 89,969,389-89,976,814 , GRCh37.p13 chr16: 90,035,797-90,043,222 CENPBD1P, AFG3L1P
    nsv6500661copy number variation1nstd223human GRCh38 chr16: 89,839,303-90,017,373 , GRCh37.p13 chr16: 89,905,711-90,083,781 DEF8, SPIRE2, 8 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
    nsv6291643copy number variation1nstd102humanUncertain significance GRCh37 chr16: 89,337,891-90,155,062 , GRCh38.p12 chr16: 89,271,483-90,088,654 DBNDD1, AFG3L1P, 34 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
    nsv6133217copy number variation1nstd213human GRCh37 chr16: 89,240,000-90,180,001 , GRCh38.p12 chr16: 89,173,592-90,113,593 AFG3L1P, GAS8-AS1, 40 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
    nsv6133037copy number variation1nstd213human GRCh37 chr16: 89,140,000-90,180,001 , GRCh38.p12 chr16: 89,073,592-90,113,593 AFG3L1P, GAS8-AS1, 44 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
    nsv5882011copy number variation1nstd209human GRCh38 chr16: 89,970,550-89,971,549 , GRCh37.p13 chr16: 90,036,958-90,037,957 CENPBD1P, AFG3L1P
    nsv5874195copy number variation2nstd209human GRCh38 chr16: 89,970,150-89,972,049 , GRCh37.p13 chr16: 90,036,558-90,038,457 CENPBD1P, AFG3L1P
    nsv5870362copy number variation1nstd209human GRCh38 chr16: 89,954,264-90,002,802 , GRCh37.p13 chr16: 90,020,672-90,069,210 DEF8, AFG3L1P, 1 more genes
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