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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5289997copy number variation1nstd204human GRCh38.p13 chr18: 24,637,466-24,638,615 , GRCh37.p13 chr18: 22,217,430-22,218,579 LINC01915
    nsv5288766copy number variation1nstd204human GRCh38.p13 chr18: 24,638,316-24,639,515 , GRCh37.p13 chr18: 22,218,280-22,219,479 LINC01915
    nsv5283914copy number variation1nstd204human GRCh38.p13 chr18: 24,626,118-24,627,217 , GRCh37.p13 chr18: 22,206,082-22,207,181 LINC01915
    nsv5280510copy number variation1nstd204human GRCh38.p13 chr18: 24,622,341-24,649,417 , GRCh37.p13 chr18: 22,202,305-22,229,381 LINC01915
    nsv5026976copy number variation1nstd200human GRCh38 chr18: 24,631,370-24,632,057 , GRCh37.p13 chr18: 22,211,334-22,212,021 LINC01915
    nsv5023996copy number variation1nstd200human GRCh38 chr18: 22,048,064-24,963,279 , GRCh37.p13 chr18: 19,628,025-22,543,243 , LOC105372028, 47 more genes
    nsv4852329copy number variation1nstd200human GRCh37 chr18: 22,211,334-22,212,021 , GRCh38.p12 chr18: 24,631,370-24,632,057 LINC01915
    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
    nsv4500282mobile element insertion1nstd166human GRCh37.p13 chr18: 22,235,650-22,235,650 , GRCh38.p12 chr18: 24,655,686-24,655,686 LINC01915
    nsv4336672sequence alteration1nstd166human GRCh37.p13 chr18: 21,176,191-70,772,863 , GRCh38.p12 chr18: 23,596,227-73,105,628 , CDH2, 557 more genes
    nsv4272070copy number variation1nstd166human GRCh37.p13 chr18: 22,202,000-22,242,000 , GRCh38.p12 chr18: 24,622,036-24,662,036 LINC01915
    nsv4265368copy number variation1nstd166human GRCh37.p13 chr18: 22,230,244-22,230,380 , GRCh38.p12 chr18: 24,650,280-24,650,416 LINC01915
    nsv4257109copy number variation1nstd166human GRCh37.p13 chr18: 22,213,575-22,213,707 , GRCh38.p12 chr18: 24,633,611-24,633,743 LINC01915
    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
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