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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148239copy number variation1nstd102humanPathogenic GRCh38 chr13: 98,343,655-110,990,677 , GRCh37.p13 chr13: 98,995,909-111,643,024 CLYBL-AS3, PPIAP24, 162 more genes
    nsv7098702complex chromosomal rearrangement24nstd230human GRCh37 chr1: 187,380,497-187,380,497 , GRCh37 chr1: 187,380,522-187,380,522 , GRCh37 chr1: 187,380,522-187,380,522 , GRCh37 chr1: 187,939,501-187,939,501 , GRCh37 chr1: 219,667,110-219,667,110 , GRCh37 chr1: 219,667,110-219,667,110 , GRCh37 chr6: 130,954,081-130,954,081 , GRCh37 chr6: 130,954,083-130,954,083 , GRCh37 chr6: 132,504,376-132,504,376 , GRCh37 chr6: 132,504,380-132,504,380 , GRCh37 chr6: 137,030,670-137,030,670 , GRCh37 chr6: 137,030,670-137,030,670 , GRCh37 chr6: 137,058,156-137,058,156 , GRCh37 chr6: 137,058,160-137,058,160 , GRCh37 chr6: 137,059,087-137,059,087 , GRCh37 chr6: 137,059,089-137,059,089 , GRCh37 chr7: 111,611,037-111,611,037 , GRCh37 chr7: 113,762,109-113,762,109 , GRCh37 chr9: 117,328,477-117,328,477 , GRCh37 chr9: 117,328,478-117,328,478 , GRCh37 chr12: 23,606,002-23,606,002 , GRCh37 chr12: 23,606,006-23,606,006 , GRCh37 chr12: 23,625,543-23,625,543 , GRCh37 chr12: 23,794,604-23,794,604 , GRCh37 chr13: 30,244,812-30,244,812 , GRCh37 chr13: 30,244,815-30,244,815 , GRCh37 chr13: 35,274,778-35,274,778 , GRCh37 chr13: 35,274,779-35,274,779 , GRCh37 chr13: 35,782,222-35,782,222 , GRCh37 chr13: 35,782,227-35,782,227 , GRCh37 chr13: 38,545,804-38,545,804 , GRCh37 chr13: 38,545,876-38,545,876 , GRCh37 chr13: 59,888,093-59,888,093 , GRCh37 chr13: 59,888,096-59,888,096 , GRCh37 chr13: 66,501,875-66,501,875 , GRCh37 chr13: 66,501,875-66,501,875 , GRCh37 chr13: 67,429,605-67,429,605 , GRCh37 chr13: 67,429,611-67,429,611 , GRCh37 chr13: 74,549,711-74,549,711 , GRCh37 chr13: 74,549,711-74,549,711 , GRCh37 chr13: 76,454,241-76,454,241 , GRCh37 chr13: 76,454,243-76,454,243 , GRCh37 chr13: 91,224,005-91,224,005 , GRCh37 chr13: 91,224,009-91,224,009 , GRCh37 chr13: 103,049,008-103,049,008 , GRCh37 chr13: 103,049,012-103,049,012 , GRCh37 chr13: 105,498,130-105,498,130 , GRCh37 chr13: 105,498,131-105,498,131 , GRCh38.p12 chr1: 187,411,365-187,411,365 , GRCh38.p12 chr1: 187,411,390-187,411,390 , GRCh38.p12 chr1: 187,411,390-187,411,390 , GRCh38.p12 chr1: 187,970,370-187,970,370 , GRCh38.p12 chr1: 219,493,768-219,493,768 , GRCh38.p12 chr1: 219,493,768-219,493,768 , GRCh38.p12 chr12: 23,453,068-23,453,068 , GRCh38.p12 chr12: 23,453,072-23,453,072 , GRCh38.p12 chr12: 23,472,609-23,472,609 , GRCh38.p12 chr12: 23,641,670-23,641,670 , GRCh38.p12 chr6: 130,632,936-130,632,936 , GRCh38.p12 chr6: 130,632,938-130,632,938 , GRCh38.p12 chr6: 132,183,236-132,183,236 , GRCh38.p12 chr6: 132,183,240-132,183,240 , GRCh38.p12 chr6: 136,709,532-136,709,532 , GRCh38.p12 chr6: 136,709,532-136,709,532 , GRCh38.p12 chr6: 136,737,018-136,737,018 , GRCh38.p12 chr6: 136,737,022-136,737,022 , GRCh38.p12 chr6: 136,737,949-136,737,949 , GRCh38.p12 chr6: 136,737,951-136,737,951 , GRCh38.p12 chr7: 111,970,982-111,970,982 , GRCh38.p12 chr7: 114,122,054-114,122,054 , GRCh38.p12 chr9: 114,566,197-114,566,197 , GRCh38.p12 chr9: 114,566,198-114,566,198 , GRCh38.p12 chr13: 29,670,675-29,670,675 , GRCh38.p12 chr13: 29,670,678-29,670,678 , GRCh38.p12 chr13: 34,700,641-34,700,641 , GRCh38.p12 chr13: 34,700,642-34,700,642 , GRCh38.p12 chr13: 35,208,085-35,208,085 , GRCh38.p12 chr13: 35,208,090-35,208,090 , GRCh38.p12 chr13: 37,971,667-37,971,667 , GRCh38.p12 chr13: 37,971,739-37,971,739 , GRCh38.p12 chr13: 59,313,959-59,313,959 , GRCh38.p12 chr13: 59,313,962-59,313,962 , GRCh38.p12 chr13: 65,927,743-65,927,743 , GRCh38.p12 chr13: 65,927,743-65,927,743 , GRCh38.p12 chr13: 66,855,473-66,855,473 , GRCh38.p12 chr13: 66,855,479-66,855,479 , GRCh38.p12 chr13: 73,975,574-73,975,574 , GRCh38.p12 chr13: 73,975,574-73,975,574 , GRCh38.p12 chr13: 75,880,105-75,880,105 , GRCh38.p12 chr13: 75,880,107-75,880,107 , GRCh38.p12 chr13: 90,571,751-90,571,751 , GRCh38.p12 chr13: 90,571,755-90,571,755 , GRCh38.p12 chr13: 102,396,658-102,396,658 , GRCh38.p12 chr13: 102,396,662-102,396,662 , GRCh38.p12 chr13: 104,845,779-104,845,779 , GRCh38.p12 chr13: 104,845,780-104,845,780 FGF14, MAP3K5, 14 more genes
    nsv7075726inversion1nstd229human GRCh38 chr13: 103,367,726-104,921,977 , GRCh37.p13 chr13: 104,020,076-105,574,328 LINC01309, RPL7P45, 8 more genes
    nsv7072238inversion1nstd229human GRCh38 chr13: 103,363,903-104,918,685 , GRCh37.p13 chr13: 104,016,253-105,571,036 RPL7P45, LOC105370340, 8 more genes
    nsv7069455inversion1nstd229human GRCh38 chr13: 104,397,285-105,386,238 , GRCh37.p13 chr13: 105,049,635-106,038,588 LOC105370343, LOC107984608, 6 more genes
    nsv7065956inversion1nstd229human GRCh38 chr13: 103,464,522-105,138,770 , GRCh37.p13 chr13: 104,116,872-105,791,121 RPL7P45, LOC107984606, 7 more genes
    nsv6954159copy number variation1nstd229human GRCh38 chr13: 104,874,868-104,883,717 , GRCh37.p13 chr13: 105,527,219-105,536,068 LOC107984608
    nsv6938700copy number variation1nstd229human GRCh38 chr13: 104,877,409-105,244,910 , GRCh37.p13 chr13: 105,529,760-105,897,261 LOC107984608, LOC105370343, 1 more genes
    nsv6638047copy number variation1nstd102humanPathogenic GRCh37 chr13: 75,268,539-115,107,733 , GRCh38.p12 chr13: 74,694,402-114,342,258 CUL4A, LOC105370373, 488 more genes
    nsv6637615copy number variation1nstd102humanPathogenic GRCh37 chr13: 93,535,335-105,788,229 , GRCh38.p12 chr13: 92,883,082-105,135,878 SNORD13G, FTLP8, 162 more genes
    nsv6637531copy number variation1nstd102humanPathogenic GRCh37 chr13: 100,334,135-110,383,902 , GRCh38.p12 chr13: 99,681,881-109,731,555 ARGLU1, LINC00343, 101 more genes
    nsv6637400copy number variation1nstd102humanPathogenic GRCh37 chr13: 97,142,120-115,107,733 , GRCh38.p12 chr13: 96,489,866-114,342,258 LOC107984609, LINC00354, 265 more genes
    nsv6637217copy number variation1nstd102humanPathogenic GRCh37 chr13: 99,421,603-115,107,733 , GRCh38.p12 chr13: 98,769,349-114,342,258 LOC107984609, CLYBL-AS2, 231 more genes
    nsv6634431copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,253,848-115,108,937 , GRCh38.p12 chr13: 18,679,708-114,343,462 MTUS2-AS1, LOC105370213, 1330 more genes
    nsv6622100copy number variation1nstd224human GRCh37 chr13: 105,464,837-105,716,018 , GRCh38.p12 chr13: 104,812,486-105,063,667 RPL7P45, LOC105370342, 5 more genes
    nsv6621770copy number variation1nstd224human GRCh37 chr13: 105,533,072-105,896,297 , GRCh38.p12 chr13: 104,880,721-105,243,946 LOC107984609, LOC105370343, 1 more genes
    nsv6493007copy number variation1nstd223human GRCh38 chr13: 104,887,001-104,887,800 , GRCh37.p13 chr13: 105,539,352-105,540,151 LOC107984608
    nsv6480840copy number variation1nstd223human GRCh38 chr13: 104,864,301-104,865,500 , GRCh37.p13 chr13: 105,516,652-105,517,851 LOC105370342, LOC107984608
    nsv6478424copy number variation1nstd223human GRCh38 chr13: 104,835,301-104,836,400 , GRCh37.p13 chr13: 105,487,652-105,488,751 LOC107984606, LOC107984608
    nsv6476686copy number variation1nstd223human GRCh38 chr13: 104,877,409-105,244,907 , GRCh37.p13 chr13: 105,529,760-105,897,258 LOC105370343, LOC107984609, 1 more genes
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