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Items: 1 to 20 of 92

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7017296copy number variation1nstd229human GRCh38 chr19: 9,774,673-9,894,587 , GRCh37.p13 chr19: 9,885,349-10,005,263 UBE2L4, FBXL12, 7 more genes
    nsv7016848copy number variation1nstd229human GRCh38 chr19: 9,846,781-9,916,685 , GRCh37.p13 chr19: 9,957,457-10,027,361 OLFM2, PIN1
    nsv7011121copy number variation1nstd229human GRCh38 chr19: 7,159,006-9,938,147 , GRCh37.p13 chr19: 7,159,017-10,048,823 , OR7G1, 117 more genes
    nsv7007503copy number variation1nstd229human GRCh38 chr19: 9,827,709-9,835,394 , GRCh37.p13 chr19: 9,938,385-9,946,070 PIN1-DT, UBL5, 1 more genes
    nsv6535327copy number variation1nstd223human GRCh38 chr19: 9,833,014-9,834,019 , GRCh37.p13 chr19: 9,943,690-9,944,695 PIN1-DT, PIN1
    nsv6291543copy number variation1nstd102humanUncertain significance GRCh37 chr19: 9,941,033-11,739,567 , GRCh38.p12 chr19: 9,830,357-11,628,752 KRI1, SHFL, 88 more genes
    nsv6133698copy number variation1nstd213human GRCh37 chr19: 2,900,000-11,490,001 , GRCh38.p12 chr19: 2,900,002-11,379,325 , TLE5, 341 more genes
    nsv6133479copy number variation1nstd213human GRCh37 chr19: 7,400,000-13,280,001 , GRCh38.p12 chr19: 7,335,095-13,169,187 , ACP5, 299 more genes
    nsv6052582copy number variation1nstd212human GRCh38 chr19: 9,845,368-9,845,498 , GRCh37.p13 chr19: 9,956,044-9,956,174 PIN1
    nsv6046349copy number variation1nstd212human GRCh38 chr19: 9,845,269-9,845,390 , GRCh37.p13 chr19: 9,955,945-9,956,066 PIN1
    nsv5937899copy number variation1nstd209human GRCh38 chr19: 9,845,252-9,845,376 , GRCh37.p13 chr19: 9,955,928-9,956,052 PIN1
    nsv5011567copy number variation1nstd200human GRCh38 chr19: 9,836,771-9,836,904 , GRCh37.p13 chr19: 9,947,447-9,947,580 PIN1
    nsv4729799copy number variation1nstd102humanUncertain significance GRCh37 chr19: 8,518,395-10,053,298 , GRCh38.p12 chr19: 8,453,511-9,942,622 ZNF426-DT, ADAMTS10, 61 more genes
    nsv4679505copy number variation1nstd189human GRCh37.p13 chr19: 9,903,732-10,322,986 , GRCh38.p12 chr19: 9,793,056-10,212,310 DNMT1, P2RY11, 18 more genes
    nsv4436244complex substitution1nstd102humanUncertain significance GRCh38.p12 chr19: 8,891,157-9,974,378 , GRCh37 chr19: 9,001,833-10,085,054 PIN1, UBE2L4, 51 more genes
    nsv4255437copy number variation1nstd166human GRCh37.p13 chr19: 9,941,000-9,948,000 , GRCh38.p12 chr19: 9,830,324-9,837,324 PIN1, UBL5, 1 more genes
    nsv4252481copy number variation1nstd166human GRCh37.p13 chr19: 9,947,447-9,947,580 , GRCh38.p12 chr19: 9,836,771-9,836,904 PIN1
    nsv3960084copy number variation1nstd168human GRCh38 chr19: 9,808,861-9,847,406 , GRCh37.p13 chr19: 9,919,537-9,958,082 PIN1, UBL5, 3 more genes
    nsv3920616copy number variation1nstd102humanLikely pathogenic NCBI36 chr19: 8,802,823-13,303,041 , GRCh37 chr19: 8,941,823-13,442,041 , GRCh38 chr19: 8,831,147-13,331,227 ACP5, GET3, 236 more genes
    nsv3912242copy number variation1nstd102humanPathogenic GRCh37 chr19: 9,846,119-11,338,677 , GRCh38 chr19: 9,735,443-11,228,001 , NCBI36 chr19: 9,707,119-11,199,677 PPAN, S1PR5, 68 more genes
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