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Items: 1 to 20 of 152

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5283601copy number variation1nstd204human GRCh38.p13 chr18: 24,322,101-24,324,600 , GRCh37.p13 chr18: 21,902,065-21,904,564 OSBPL1A, MIR320C2
    nsv5023996copy number variation1nstd200human GRCh38 chr18: 22,048,064-24,963,279 , GRCh37.p13 chr18: 19,628,025-22,543,243 , LOC105372028, 47 more genes
    nsv4852323copy number variation1nstd200human GRCh37 chr18: 21,900,653-21,901,180 , GRCh38.p12 chr18: 24,320,689-24,321,216 MIR320C2, OSBPL1A
    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
    nsv4620072copy number variation1nstd183human GRCh37 chr18: 21,893,529-21,909,237 , GRCh38.p12 chr18: 24,313,565-24,329,273 OSBPL1A, MIR320C2
    nsv4457647copy number variation1nstd102humanUncertain significance GRCh37 chr18: 21,391,033-21,964,238 , GRCh38.p12 chr18: 23,811,069-24,384,274 TTC39C, LAMA3, 8 more genes
    nsv4336672sequence alteration1nstd166human GRCh37.p13 chr18: 21,176,191-70,772,863 , GRCh38.p12 chr18: 23,596,227-73,105,628 , CDH2, 557 more genes
    nsv3958216copy number variation1nstd168human GRCh38 chr18: 24,292,794-24,361,008 , GRCh37.p13 chr18: 21,872,758-21,940,972 OSBPL1A, MIR320C2
    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
    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
    nsv3918488copy number variation1nstd102humanPathogenic NCBI36 chr18: 43,345-76,068,860 , GRCh38 chr18: 53,345-80,209,986 , GRCh37 chr18: 53,345-77,967,869 LOC105372027, ASXL3, 945 more genes
    nsv3916426copy number variation1nstd102humanPathogenic GRCh37 chr18: 149,089-77,992,274 , NCBI36 chr18: 139,089-76,093,265 , GRCh38 chr18: 149,089-80,234,391 TPGS2, TWSG1-DT, 941 more genes
    nsv3916358copy number variation1nstd102humanPathogenic GRCh38 chr18: 20,941,324-40,360,620 , NCBI36 chr18: 16,775,283-36,194,582 , GRCh37 chr18: 18,521,285-37,940,584 MIR4741, LOC105372029, 220 more genes
    nsv3915938copy number variation1nstd102humanPathogenic GRCh37 chr18: 18,569,723-77,967,869 , GRCh38 chr18: 20,989,762-80,209,986 , NCBI36 chr18: 16,823,721-76,068,860 LOC105372061, LOC107985171, 670 more genes
    nsv3914075copy number variation1nstd102humanPathogenic GRCh37 chr18: 18,540,281-26,181,841 , NCBI36 chr18: 16,794,279-24,435,839 , GRCh38 chr18: 20,960,320-28,601,877 LINC01900, HRH4, 106 more genes
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