U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 946

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7057909inversion1nstd229human GRCh38 chr7: 114,144,372-114,144,406 , GRCh37.p13 chr7: 113,784,427-113,784,461 FOXP2
    nsv7053845inversion1nstd229human GRCh38 chr7: 114,436,384-114,436,583 , GRCh37.p13 chr7: 114,076,439-114,076,638 FOXP2
    nsv7053373inversion1nstd229human GRCh38 chr7: 114,378,977-114,379,030 , GRCh37.p13 chr7: 114,019,032-114,019,085 FOXP2
    nsv7051954inversion1nstd229human GRCh38 chr7: 114,480,516-114,516,893 , GRCh37.p13 chr7: 114,120,571-114,156,948 FOXP2
    nsv7050056inversion1nstd229human GRCh38 chr7: 114,436,167-114,436,726 , GRCh37.p13 chr7: 114,076,222-114,076,781 FOXP2
    nsv7049829inversion1nstd229human GRCh38 chr7: 114,093,668-114,093,695 , GRCh37.p13 chr7: 113,733,723-113,733,750 FOXP2
    nsv7046050inversion1nstd229human GRCh38 chr7: 114,287,423-114,292,668 , GRCh37.p13 chr7: 113,927,478-113,932,723 FOXP2
    nsv7043165inversion1nstd229human GRCh38 chr7: 114,370,647-114,370,670 , GRCh37.p13 chr7: 114,010,702-114,010,725 FOXP2
    nsv6837850copy number variation1nstd229human GRCh38 chr7: 114,305,929-114,305,957 , GRCh37.p13 chr7: 113,945,984-113,946,012 FOXP2
    nsv6837321copy number variation1nstd229human GRCh38 chr7: 114,672,657-114,675,455 , GRCh37.p13 chr7: 114,312,712-114,315,510 FOXP2
    nsv6836924copy number variation1nstd229human GRCh38 chr7: 114,208,318-114,213,319 , GRCh37.p13 chr7: 113,848,373-113,853,374 FOXP2
    nsv6836471copy number variation1nstd229human GRCh38 chr7: 114,313,463-114,313,758 , GRCh37.p13 chr7: 113,953,518-113,953,813 FOXP2
    nsv6835953copy number variation1nstd229human GRCh38 chr7: 114,469,605-114,469,842 , GRCh37.p13 chr7: 114,109,660-114,109,897 FOXP2
    nsv6835792copy number variation1nstd229human GRCh38 chr7: 114,084,201-114,087,600 , GRCh37.p13 chr7: 113,724,256-113,727,655 FOXP2
    nsv6834869copy number variation1nstd229human GRCh38 chr7: 114,349,383-114,353,161 , GRCh37.p13 chr7: 113,989,438-113,993,216 FOXP2
    nsv6834680copy number variation1nstd229human GRCh38 chr7: 114,216,865-114,224,854 , GRCh37.p13 chr7: 113,856,920-113,864,909 FOXP2
    nsv6834223copy number variation1nstd229human GRCh38 chr7: 114,141,601-114,144,300 , GRCh37.p13 chr7: 113,781,656-113,784,355 FOXP2
    nsv6833283copy number variation1nstd229human GRCh38 chr7: 114,173,226-114,274,251 , GRCh37.p13 chr7: 113,813,281-113,914,306 FOXP2
    nsv6832356copy number variation1nstd229human GRCh38 chr7: 114,677,473-114,687,530 , GRCh37.p13 chr7: 114,317,528-114,327,585 FOXP2
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center