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Items: 1 to 20 of 162

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5674237copy number variation1nstd102humanPathogenic GRCh38 chr4: 51,891,814-76,009,719 , GRCh37.p13 chr4: 52,757,980-76,930,872 FTLP10, RNU6-410P, 335 more genes
    nsv5352961translocation1nstd200human GRCh38 chr4: 55,078,361-55,078,361 , GRCh38 chr4: 55,078,449-55,078,449 , GRCh37.p13 chr4: 55,944,528-55,944,528 , GRCh37.p13 chr4: 55,944,616-55,944,616 KDR
    nsv5083112mobile element insertion1nstd203human GRCh38 chr4: 55,100,917-55,100,930 , GRCh37.p13 chr4: 55,967,084-55,967,097 KDR
    nsv5039232inversion1nstd200human GRCh38 chr4: 9,660,225-57,055,279 , GRCh37.p13 chr4: 9,661,849-57,921,445 , KRT18P63, 533 more genes
    nsv5034204inversion1nstd200human GRCh38 chr4: 45,103,677-117,623,076 , GRCh37.p13 chr4: 45,105,694-118,544,231 , LOC100129728, 913 more genes
    nsv4878267inversion1nstd200human GRCh37 chr4: 45,105,694-118,544,231 , GRCh38.p12 chr4: 45,103,677-117,623,076 , MIR367, 913 more genes
    nsv4761770inversion1nstd199human GRCh37 chr4: 34,988-191,015,248 , GRCh38.p12 chr4: 34,988-190,094,093 , ADD1, 2433 more genes
    nsv4758212inversion1nstd199human GRCh37 chr4: 30,775-191,019,445 , GRCh38.p12 chr4: 30,775-190,098,290 , ADD1, 2433 more genes
    nsv4754592inversion1nstd199human GRCh37 chr4: 27,111-191,020,337 , GRCh38.p12 chr4: 27,111-190,099,182 , ADD1, 2433 more genes
    nsv4753570inversion1nstd199human GRCh37 chr4: 19,034-191,028,414 , GRCh38.p12 chr4: 19,034-190,107,259 , ADD1, 2434 more genes
    nsv4751554inversion1nstd199human GRCh37 chr4: 18,939-191,034,785 , GRCh38.p12 chr4: 18,939-190,113,630 , ADD1, 2434 more genes
    nsv4539925insertion1nstd166human GRCh37.p13 chr4: 55,985,993-55,985,993 , GRCh38.p12 chr4: 55,119,826-55,119,826 KDR
    nsv4521809copy number variation1nstd166human GRCh37.p13 chr4: 55,983,127-55,983,178 , GRCh38.p12 chr4: 55,116,960-55,117,011 KDR
    nsv4108054copy number variation1nstd166human GRCh37.p13 chr4: 55,944,528-55,944,616 , GRCh38.p12 chr4: 55,078,361-55,078,449 KDR
    nsv4105483copy number variation1nstd166human GRCh37.p13 chr4: 55,963,249-55,963,389 , GRCh38.p12 chr4: 55,097,082-55,097,222 KDR
    nsv3919213copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,766,026-60,850,197 , NCBI36 chr4: 52,460,783-60,532,792 , GRCh38 chr4: 51,899,860-59,984,479 LNX1-AS1, RPL7AP31, 106 more genes
    nsv3917232copy number variation1nstd102humanPathogenic NCBI36 chr4: 54,759,525-62,818,428 , GRCh38 chr4: 54,198,601-62,270,115 , GRCh37 chr4: 55,064,768-63,135,833 CLOCK, TMEM165, 84 more genes
    nsv3914335copy number variation1nstd102humanPathogenic GRCh37 chr4: 44,358,218-63,111,600 , NCBI36 chr4: 44,052,975-62,794,195 , GRCh38 chr4: 44,356,201-62,245,882 RPL22P13, RNA5SP161, 178 more genes
    nsv3913938copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,736,191-55,968,559 , GRCh38 chr4: 51,870,025-55,102,392 , NCBI36 chr4: 52,430,948-55,663,316 LINC02260, ERVMER34-1, 42 more genes
    nsv3913811copy number variation1nstd102humanPathogenic GRCh38 chr4: 51,831,622-97,505,618 , GRCh37 chr4: 52,697,788-98,426,769 , NCBI36 chr4: 52,392,545-98,645,792 LOC105377297, HNRNPA1P56, 582 more genes
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