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Items: 1 to 20 of 31

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3917126copy number variation1nstd102humanPathogenic GRCh38 chr4: 116,630,862-145,429,900 , NCBI36 chr4: 117,771,466-146,570,502 , GRCh37 chr4: 117,552,018-146,351,052 UCP1, SETD7, 294 more genes
    nsv3912421copy number variation1nstd102humanPathogenic NCBI36 chr4: 129,260,477-143,571,978 , GRCh37 chr4: 129,041,027-143,352,528 , GRCh38 chr4: 128,119,872-142,431,375 UCP1, PCDH10-DT, 120 more genes
    nsv6291168copy number variation1nstd102humanPathogenic GRCh37 chr4: 138,289,049-145,923,298 , GRCh38.p12 chr4: 137,367,895-145,002,146 UCP1, LOC105377447, 92 more genes
    nsv4674499copy number variation1nstd102humanPathogenic GRCh37 chr4: 139,531,815-146,095,109 , GRCh38.p12 chr4: 138,610,661-145,173,957 UCP1, GUSBP5, 77 more genes
    nsv6290718copy number variation1nstd102humanPathogenic GRCh37 chr4: 136,529,470-141,564,812 , GRCh38.p12 chr4: 135,608,315-140,643,658 UCP1, MGARP, 61 more genes
    nsv4674743copy number variation1nstd102humanPathogenic GRCh37 chr4: 137,901,978-141,527,647 , GRCh38.p12 chr4: 136,980,824-140,606,493 UCP1, RAB33B-AS1, 56 more genes
    nsv3873978copy number variation1nstd102humanPathogenic GRCh37 chr4: 11,525-191,028,879 , GRCh38.p12 chr4: 11,525-190,107,724 UCP1, LOC100422029, 2358 more genes
    nsv3876533copy number variation1nstd102humanPathogenic GRCh37 chr4: 49,450-190,963,766 , GRCh38.p12 chr4: 49,556-190,042,611 UCP1, LOC100420289, 2347 more genes
    nsv3884499copy number variation1nstd102humanPathogenic GRCh37 chr4: 12,440-190,904,441 , GRCh38.p12 chr4: 12,440-189,983,286 UCP1, MTND4LP29, 2341 more genes
    nsv3880085copy number variation2nstd102humanPathogenic GRCh37 chr4: 68,346-190,957,473 , GRCh38.p12 chr4: 68,454-190,036,318 UCP1, LOC112268460, 2345 more genes
    nsv3883791copy number variation1nstd102humanPathogenic GRCh37 chr4: 49,450-190,915,650 , GRCh38.p12 chr4: 49,556-189,994,495 UCP1, LOC105377343, 2341 more genes
    nsv3875534copy number variation1nstd102humanPathogenic GRCh37 chr4: 93,071,152-190,957,473 , GRCh38.p12 chr4: 92,150,001-190,036,318 UCP1, KLKB1, 1118 more genes
    nsv6291432copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354 UCP1, SNHG27, 1091 more genes
    nsv3874596copy number variation1nstd102humanPathogenic GRCh37 chr4: 109,199,664-189,752,726 , GRCh38.p12 chr4: 108,278,508-188,831,572 UCP1, RPL6P12, 938 more genes
    nsv3924008copy number variation1nstd102humanPathogenic GRCh38 chr4: 118,065,569-190,042,639 , GRCh37 chr4: 118,986,724-190,828,225 , NCBI36 chr4: 119,206,172-191,200,788 UCP1, PPID, 828 more genes
    nsv3874610copy number variation1nstd102humanPathogenic GRCh37 chr4: 119,437,495-190,904,301 , GRCh38.p12 chr4: 118,516,340-189,983,146 UCP1, OTUD4, 813 more genes
    nsv3918110copy number variation1nstd102humanPathogenic NCBI36 chr4: 122,658,828-191,220,419 , GRCh38 chr4: 121,518,223-190,062,270 , GRCh37 chr4: 122,439,378-190,828,225 UCP1, SCRG1, 770 more genes
    nsv4455301copy number variation1nstd102humanPathogenic GRCh37 chr4: 124,873,497-185,278,662 , GRCh38.p12 chr4: 123,952,342-184,357,509 UCP1, SMARCA5, 633 more genes
    nsv3911855copy number variation1nstd102humanPathogenic GRCh38 chr4: 125,432,943-185,761,887 , GRCh37 chr4: 126,354,098-186,683,041 , NCBI36 chr4: 126,573,548-186,920,035 UCP1, RPL26P16, 656 more genes
    nsv3911177copy number variation1nstd102humanPathogenic GRCh38 chr4: 131,985,253-190,095,391 , NCBI36 chr4: 133,125,858-191,250,527 , GRCh37 chr4: 132,906,408-190,828,225 UCP1, SNORD73B, 683 more genes
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