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Items: 1 to 20 of 133

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7074674inversion1nstd229human GRCh38 chr12: 100,072,817-104,989,567 , GRCh37.p13 chr12: 100,466,595-105,383,345 SYCP3, GOLGA2P5, 84 more genes
    nsv7068612inversion1nstd229human GRCh38 chr12: 100,083,131-104,989,539 , GRCh37.p13 chr12: 100,476,909-105,383,317 EID3, RNU6-1068P, 84 more genes
    nsv7063973inversion1nstd229human GRCh38 chr12: 103,801,289-104,249,958 , GRCh37.p13 chr12: 104,195,067-104,643,736 MIR3652, HCFC2, 13 more genes
    nsv6930893copy number variation1nstd229human GRCh38 chr12: 103,962,558-103,962,639 , GRCh37.p13 chr12: 104,356,336-104,356,417 UQCC6
    nsv6924587copy number variation1nstd229human GRCh38 chr12: 103,949,064-103,951,587 , GRCh37.p13 chr12: 104,342,842-104,345,365 UQCC6
    nsv6923034copy number variation1nstd229human GRCh38 chr12: 103,827,059-103,994,464 , GRCh37.p13 chr12: 104,220,837-104,388,242 GLT8D2, TTC41P, 6 more genes
    nsv6922635copy number variation1nstd229human GRCh38 chr12: 96,115,345-104,800,221 , GRCh37.p13 chr12: 96,509,123-105,193,999 RNY1P16, CHST11, 121 more genes
    nsv6637829copy number variation1nstd102humanUncertain significance GRCh37 chr12: 103,588,380-105,161,579 , GRCh38.p12 chr12: 103,194,602-104,767,801 TDG, MIR3922, 24 more genes
    nsv6581722inversion1nstd223human GRCh38 chr12: 103,959,617-103,960,042 , GRCh37.p13 chr12: 104,353,395-104,353,820 UQCC6
    nsv6291583copy number variation1nstd102humanPathogenic GRCh37 chr12: 104,230,462-111,984,801 , GRCh38.p12 chr12: 103,836,684-111,546,997 LOC105369964, LOC644746, 147 more genes
    nsv6143026copy number variation1nstd206human GRCh38 chr12: 48,500,915-111,724,058 , GRCh37.p13 chr12: 48,894,698-112,161,862 , LINC00592, 1206 more genes
    nsv6132318copy number variation1nstd213human GRCh37 chr12: 104,010,000-104,380,001 , GRCh38.p12 chr12: 103,616,222-103,986,223 TDG, HSP90B1, 7 more genes
    nsv6132210copy number variation1nstd213human GRCh37 chr12: 103,750,000-105,110,001 , GRCh38.p12 chr12: 103,356,222-104,716,223 HSP90B1, RNA5SP370, 24 more genes
    nsv5365196translocation1nstd200human GRCh38 chr12: 125,316,602-125,316,602 , GRCh38 chr12: 103,965,852-103,965,852 , GRCh37.p13 chr12: 104,359,630-104,359,630 , GRCh37.p13 chr12: 125,801,148-125,801,148 TDG, TMEM132B, 1 more genes
    nsv5342944translocation1nstd200human GRCh37 chr12: 104,359,630-104,359,630 , GRCh37 chr12: 125,801,148-125,801,148 , GRCh38.p12 chr12: 103,965,852-103,965,852 , GRCh38.p12 chr12: 125,316,602-125,316,602 TDG, TMEM132B, 1 more genes
    nsv5322275translocation1nstd204human GRCh38.p13 chr12: 103,965,852-103,965,852 , GRCh38.p13 chr12: 125,316,602-125,316,602 , GRCh37.p13 chr12: 104,359,630-104,359,630 , GRCh37.p13 chr12: 125,801,148-125,801,148 TDG, TMEM132B, 1 more genes
    nsv5037136inversion1nstd200human GRCh38 chr12: 69,787,024-109,882,221 , GRCh37.p13 chr12: 70,180,804-110,320,026 , RPL23AP68, 540 more genes
    nsv4993629copy number variation1nstd200human GRCh38 chr12: 103,943,825-103,949,603 , GRCh37.p13 chr12: 104,337,603-104,343,381 UQCC6, HSP90B1
    nsv4886161inversion1nstd200human GRCh37 chr12: 70,180,810-110,320,027 , GRCh38.p12 chr12: 69,787,030-109,882,222 , LOC728739, 540 more genes
    nsv4756208inversion1nstd199human GRCh37 chr12: 104,359,633-125,801,147 , GRCh38.p12 chr12: 103,965,855-125,316,601 , ACACB, 453 more genes
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