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Items: 1 to 20 of 523

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6129452insertion1nstd186human GRCh37 chr21: 11,063,075-11,063,075 , GRCh38.p12 chr21: 10,449,382-10,449,382 , GRCh38.p12 chr13|NW_011332699.1: 127,919-127,919 BAGE5, BAGE2
    nsv6116166copy number variation1nstd186human GRCh37 chr21: 11,054,457-11,097,657 , GRCh38.p12 chr21: 10,414,800-10,458,000 , GRCh38.p12 chr13|NW_011332699.1: 93,539-136,534 BAGE5, BAGE2
    nsv5341914translocation1nstd200human GRCh37 chr7: 151,975,580-151,975,580 , GRCh37 chr21: 11,063,234-11,063,234 , GRCh38.p12 chr21: 10,449,223-10,449,223 , GRCh38.p12 chr7: 152,278,495-152,278,495 , GRCh38.p12 chr13|NW_011332699.1: 127,760-127,760 KMT2C, BAGE5, 1 more genes
    nsv5340065translocation1nstd200human GRCh37 chr7: 151,979,777-151,979,777 , GRCh37 chr21: 11,067,043-11,067,043 , GRCh38.p12 chr21: 10,445,414-10,445,414 , GRCh38.p12 chr7: 152,282,692-152,282,692 , GRCh38.p12 chr13|NW_011332699.1: 123,958-123,958 KMT2C, BAGE5, 1 more genes
    nsv5337221translocation1nstd200human GRCh37 chr7: 152,099,188-152,099,188 , GRCh37 chr21: 11,097,543-11,097,543 , GRCh38.p12 chr21: 10,414,914-10,414,914 , GRCh38.p12 chr7: 152,402,103-152,402,103 , GRCh38.p12 chr13|NW_011332699.1: 93,539-93,539 KMT2C, BAGE5, 1 more genes
    nsv5333168translocation1nstd200human GRCh37 chr7: 152,085,957-152,085,957 , GRCh37 chr21: 11,092,540-11,092,540 , GRCh38.p12 chr21: 10,419,917-10,419,917 , GRCh38.p12 chr7: 152,388,872-152,388,872 , GRCh38.p12 chr13|NW_011332699.1: 98,504-98,504 KMT2C, BAGE5, 1 more genes
    nsv5330979translocation1nstd200human GRCh37 chr7: 151,979,130-151,979,130 , GRCh37 chr21: 11,066,992-11,066,992 , GRCh38.p12 chr21: 10,445,465-10,445,465 , GRCh38.p12 chr7: 152,282,045-152,282,045 , GRCh38.p12 chr13|NW_011332699.1: 124,009-124,009 KMT2C, BAGE5, 1 more genes
    nsv4759703insertion1nstd199human GRCh37 chr21: 11,067,042-11,067,042 , GRCh38.p12 chr21: 10,445,415-10,445,415 , GRCh38.p12 chr13|NW_011332699.1: 123,959-123,959 BAGE5, BAGE2
    nsv4758100inversion1nstd199human GRCh38.p12 chr21: 10,426,271-10,427,036 , GRCh37 chr21: 11,085,421-11,086,186 , GRCh38.p12 chr13|NW_011332699.1: 104,855-105,585 BAGE5, BAGE2
    nsv4748103copy number variation1nstd199human GRCh37 chr21: 11,089,824-11,092,577 , GRCh38.p12 chr21: 10,419,880-10,422,633 , GRCh38.p12 chr13|NW_011332699.1: 98,467-101,221 BAGE5, BAGE2
    nsv4732420copy number variation1nstd199human GRCh38.p12 chr21: 10,334,869-10,567,120 , GRCh37 chr21: 10,945,337-11,177,588 , GRCh38.p12 chr13|NW_011332699.1: 1-169,908 TPTE, BAGE5, 2 more genes
    nsv4716158translocation1nstd195human GRCh38.p12 chr21: 10,424,234-10,424,234 , GRCh37 chr21: 11,088,223-11,088,223 , GRCh37 chr7: 152,084,287-152,084,287 , GRCh38.p12 chr7: 152,387,202-152,387,202 , GRCh38.p12 chr13|NW_011332699.1: 102,818-102,818 KMT2C, BAGE5, 1 more genes
    nsv4714072translocation1nstd195human GRCh38.p12 chr21: 10,466,695-10,466,695 , GRCh37 chr21: 11,045,762-11,045,762 , GRCh37 chr7: 151,958,364-151,958,364 , GRCh38.p12 chr7: 152,261,279-152,261,279 , GRCh38.p12 chr13|NW_011332699.1: 145,228-145,228 KMT2C, BAGE5, 1 more genes
    nsv4713244translocation1nstd195human GRCh38.p12 chr21: 10,449,164-10,449,164 , GRCh37 chr21: 11,063,293-11,063,293 , GRCh37 chr7: 151,975,829-151,975,829 , GRCh38.p12 chr7: 152,278,744-152,278,744 , GRCh38.p12 chr13|NW_011332699.1: 127,701-127,701 KMT2C, BAGE5, 1 more genes
    nsv4712517translocation1nstd195human GRCh38.p12 chr21: 10,424,234-10,424,234 , GRCh37 chr21: 11,088,223-11,088,223 , GRCh37 chr7: 152,084,287-152,084,287 , GRCh38.p12 chr7: 152,387,202-152,387,202 , GRCh38.p12 chr13|NW_011332699.1: 102,818-102,818 KMT2C, BAGE5, 1 more genes
    nsv4711309translocation1nstd195human GRCh38.p12 chr21: 10,445,591-10,445,591 , GRCh37 chr21: 11,066,866-11,066,866 , GRCh37 chr7: 151,979,438-151,979,438 , GRCh38.p12 chr7: 152,282,353-152,282,353 , GRCh38.p12 chr13|NW_011332699.1: 124,135-124,135 KMT2C, BAGE5, 1 more genes
    nsv4710786copy number variation1nstd195human GRCh37 chr21: 11,020,151-11,158,351 , GRCh38.p12 chr21: 10,354,106-10,492,306 , GRCh38.p12 chr13|NW_011332699.1: 16,879-169,908 BAGE5, BAGE2, 1 more genes
    nsv4710717translocation1nstd195human GRCh38.p12 chr21: 10,455,222-10,455,222 , GRCh37 chr21: 11,057,235-11,057,235 , GRCh37 chr7: 151,969,660-151,969,660 , GRCh38.p12 chr7: 152,272,575-152,272,575 , GRCh38.p12 chr13|NW_011332699.1: 133,760-133,760 KMT2C, BAGE5, 1 more genes
    nsv4710685translocation1nstd195human GRCh38.p12 chr21: 10,425,382-10,425,382 , GRCh37 chr21: 11,087,075-11,087,075 , GRCh37 chr7: 152,083,169-152,083,169 , GRCh38.p12 chr7: 152,386,084-152,386,084 , GRCh38.p12 chr13|NW_011332699.1: 103,966-103,966 KMT2C, BAGE5, 1 more genes
    nsv4710062copy number variation1nstd195human GRCh37 chr21: 11,012,351-11,160,851 , GRCh38.p12 chr21: 10,351,606-10,500,106 , GRCh38.p12 chr13|NW_011332699.1: 14,388-169,908 BAGE5, BAGE2, 1 more genes
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