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Items: 1 to 20 of 197

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5151867mobile element insertion1nstd203human GRCh38 chr18: 24,471,606-24,471,633 , GRCh37.p13 chr18: 22,051,570-22,051,597 HRH4
    nsv5141847mobile element insertion1nstd203human GRCh38 chr18: 24,461,541-24,461,553 , GRCh37.p13 chr18: 22,041,505-22,041,517 HRH4
    nsv5026974copy number variation1nstd200human GRCh38 chr18: 24,461,193-24,462,016 , GRCh37.p13 chr18: 22,041,157-22,041,980 HRH4
    nsv5026973copy number variation1nstd200human GRCh38 chr18: 24,452,527-24,460,601 , GRCh37.p13 chr18: 22,032,491-22,040,565 HRH4, IMPACT
    nsv5024015copy number variation1nstd200human GRCh38 chr18: 24,474,833-24,482,159 , GRCh37.p13 chr18: 22,054,797-22,062,123 HRH4
    nsv5023996copy number variation1nstd200human GRCh38 chr18: 22,048,064-24,963,279 , GRCh37.p13 chr18: 19,628,025-22,543,243 , LOC105372028, 47 more genes
    nsv4852328copy number variation1nstd200human GRCh37 chr18: 22,041,157-22,041,980 , GRCh38.p12 chr18: 24,461,193-24,462,016 HRH4
    nsv4676155copy number variation1nstd102humanPathogenic GRCh37 chr18: 20,689,919-49,455,212 , GRCh38.p12 chr18: 23,109,955-51,928,842 KLHL14, RPL23AP77, 318 more genes
    nsv4622834copy number variation1nstd183human GRCh37 chr18: 22,057,517-22,060,915 , GRCh38.p12 chr18: 24,477,553-24,480,951 HRH4
    nsv4503983mobile element insertion1nstd166human GRCh37.p13 chr18: 22,041,505-22,041,505 , GRCh38.p12 chr18: 24,461,541-24,461,541 HRH4
    nsv4336672sequence alteration1nstd166human GRCh37.p13 chr18: 21,176,191-70,772,863 , GRCh38.p12 chr18: 23,596,227-73,105,628 , CDH2, 557 more genes
    nsv4259791copy number variation1nstd166human GRCh37.p13 chr18: 22,054,812-22,062,106 , GRCh38.p12 chr18: 24,474,848-24,482,142 HRH4
    nsv3924706copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,227-78,014,123 , GRCh38 chr18: 136,227-80,256,240 , NCBI36 chr18: 126,227-76,115,097 LOC100420948, NPM1P2, 941 more genes
    nsv3924638copy number variation1nstd102humanPathogenic GRCh38 chr18: 20,962,119-74,691,446 , NCBI36 chr18: 16,796,078-70,532,390 , GRCh37 chr18: 18,542,080-72,403,402 HMGN1P30, LOC107985134, 596 more genes
    nsv3924351copy number variation1nstd102humanPathogenic NCBI36 chr18: 108,760-76,113,817 , GRCh38 chr18: 118,760-80,254,946 , GRCh37 chr18: 118,760-78,012,829 MIX23P1, LOC105372087, 942 more genes
    nsv3923838copy number variation1nstd102humanPathogenic NCBI36 chr18: 138,963-76,103,255 , GRCh37 chr18: 148,963-78,002,264 , GRCh38 chr18: 148,963-80,244,381 WDR7-OT1, HMGN1P30, 941 more genes
    nsv3920818copy number variation1nstd102humanPathogenic NCBI36 chr18: 15,370,696-76,117,153 , GRCh37.p13 chr18: 15,380,696-78,016,181 , GRCh38.p12 chr18: 15,380,697-80,258,298 AQP4-AS1, SERPINB8, 670 more genes
    nsv3920624copy number variation1nstd102humanUncertain significance GRCh37 chr18: 21,991,957-24,208,087 , NCBI36 chr18: 20,245,955-22,462,085 , GRCh38 chr18: 24,411,993-26,628,123 EIF4A3P1, SINHCAFP1, 29 more genes
    nsv3920487copy number variation1nstd102humanPathogenic NCBI36 chr18: 16,783,337-30,197,417 , GRCh38 chr18: 20,949,378-34,363,455 , GRCh37 chr18: 18,529,339-31,943,419 CCDC178, RNA5SP452, 159 more genes
    nsv3919004copy number variation1nstd102humanPathogenic GRCh38 chr18: 136,226-80,256,240 , GRCh37 chr18: 136,226-78,014,123 , NCBI36 chr18: 126,226-76,115,097 LIVAR, LINC03069, 941 more genes
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