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Items: 1 to 20 of 176

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093820copy number variation1nstd102humanUncertain significance GRCh37 chr11: 101,374,735-103,349,981 , GRCh38.p12 chr11: 101,504,004-103,479,253 WTAPP1, TMEM123, 40 more genes
    nsv7068895inversion1nstd229human GRCh38 chr11: 100,518,680-109,308,656 , GRCh37.p13 chr11: 100,389,411-109,179,383 LINC02719, RNA5SP349, 121 more genes
    nsv7061741inversion1nstd229human GRCh38 chr11: 100,793,881-105,425,000 , GRCh37.p13 chr11: 100,664,612-105,295,727 MTND1P36, LOC102723862, 75 more genes
    nsv6917199copy number variation1nstd229human GRCh38 chr11: 102,353,565-102,366,657 , GRCh37.p13 chr11: 102,224,296-102,237,388 BIRC2
    nsv6907947copy number variation1nstd229human GRCh38 chr11: 102,119,146-102,385,954 , GRCh37.p13 chr11: 101,989,877-102,256,685 RPS6P17, LOC105369460, 4 more genes
    nsv6904344copy number variation1nstd229human GRCh38 chr11: 102,352,968-102,360,451 , GRCh37.p13 chr11: 102,223,699-102,231,182 BIRC2
    nsv6901019copy number variation1nstd229human GRCh38 chr11: 102,326,501-102,376,200 , GRCh37.p13 chr11: 102,197,232-102,246,931 BIRC3, BIRC2
    nsv6898519copy number variation1nstd229human GRCh38 chr11: 101,614,768-102,883,244 , GRCh37.p13 chr11: 101,485,499-102,702,496 PLS1P1, MMP3, 26 more genes
    nsv6637687copy number variation1nstd102humanPathogenic GRCh37 chr11: 101,371,503-109,306,519 , GRCh38.p12 chr11: 101,500,772-109,435,793 GRIA4, MTND1P36, 111 more genes
    nsv6637671copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 98,770,072-104,602,846 , GRCh38.p12 chr11: 98,899,342-104,732,118 BIRC2, BIRC3, 67 more genes
    nsv6637396copy number variation1nstd102humanPathogenic GRCh37 chr11: 81,478,509-104,667,040 , GRCh38.p12 chr11: 81,767,467-104,796,313 LOC107984375, RN7SL222P, 295 more genes
    nsv6637174copy number variation1nstd102humanUncertain significance GRCh37 chr11: 99,059,204-103,281,943 , GRCh38.p12 chr11: 99,188,473-103,411,215 TMEM123, LOC100418997, 55 more genes
    nsv6586331inversion1nstd223human GRCh38 chr11: 102,351,336-102,352,097 , GRCh37.p13 chr11: 102,222,067-102,222,828 BIRC2
    nsv6582485inversion1nstd223human GRCh38 chr11: 100,023,537-103,679,304 , GRCh37.p13 chr11: 99,894,269-103,550,032 BOLA3P1, LOC100190922, 56 more genes
    nsv6470242copy number variation1nstd223human GRCh38 chr11: 102,352,968-102,360,445 , GRCh37.p13 chr11: 102,223,699-102,231,176 BIRC2
    nsv6464230copy number variation1nstd223human GRCh38 chr11: 102,119,146-102,385,954 , GRCh37.p13 chr11: 101,989,877-102,256,685 LOC105369460, BIRC3, 4 more genes
    nsv6458464copy number variation1nstd223human GRCh38 chr11: 102,342,801-102,353,700 , GRCh37.p13 chr11: 102,213,532-102,224,431 BIRC2
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6309019copy number variation2nstd102humanPathogenic GRCh37 chr11: 101,323,686-103,349,981 , GRCh38.p12 chr11: 101,452,955-103,479,253 RPL21P96, RNU6-952P, 40 more genes
    nsv6290834copy number variation1nstd102humanUncertain significance GRCh37 chr11: 85,422,071-118,022,671 , GRCh38.p12 chr11: 85,711,028-118,151,956 CARD17P, RNA5SP350, 480 more genes
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