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Items: 1 to 20 of 494

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057058inversion1nstd229human GRCh38 chr4: 165,065,528-168,877,636 , GRCh37.p13 chr4: 165,986,680-169,798,787 DDX60L, RNA5SP170, 33 more genes
    nsv7055423inversion1nstd229human GRCh38 chr4: 164,775,658-165,238,157 , GRCh37.p13 chr4: 165,696,810-166,159,309 TRIM61, SMIM31, 17 more genes
    nsv7052357inversion1nstd229human GRCh38 chr4: 165,071,350-165,072,385 , GRCh37.p13 chr4: 165,992,502-165,993,537 TMEM192
    nsv6751864copy number variation1nstd229human GRCh38 chr4: 164,039,828-165,202,299 , GRCh37.p13 chr4: 164,960,980-166,123,451 LOC391711, TRIM75, 21 more genes
    nsv6751820copy number variation1nstd229human GRCh38 chr4: 164,784,634-165,203,278 , GRCh37.p13 chr4: 165,705,786-166,124,430 LOC100420385, TRIM60, 16 more genes
    nsv6751711copy number variation1nstd229human GRCh38 chr4: 165,069,827-165,070,016 , GRCh37.p13 chr4: 165,990,979-165,991,168 TMEM192
    nsv6750623copy number variation1nstd229human GRCh38 chr4: 164,776,894-165,258,284 , GRCh37.p13 chr4: 165,698,046-166,179,436 TMEM192, TRIM75, 18 more genes
    nsv6749186copy number variation1nstd229human GRCh38 chr4: 165,032,062-165,104,704 , GRCh37.p13 chr4: 165,953,214-166,025,856 TMEM192, TRIM75, 1 more genes
    nsv6740739copy number variation1nstd229human GRCh38 chr4: 165,093,385-165,094,290 , GRCh37.p13 chr4: 166,014,537-166,015,442 TMEM192
    nsv6740482copy number variation1nstd229human GRCh38 chr4: 164,057,383-165,303,005 , GRCh37.p13 chr4: 164,978,535-166,224,157 TRIM60P14, LOC391711, 24 more genes
    nsv6738361copy number variation1nstd229human GRCh38 chr4: 164,957,591-165,077,094 , GRCh37.p13 chr4: 165,878,743-165,998,246 FAM218A, TRIM75, 7 more genes
    nsv6636318copy number variation1nstd102humanUncertain significance GRCh37 chr4: 161,461,677-166,911,259 , GRCh38.p12 chr4: 160,540,525-165,990,107 LOC107986325, NACA3P, 60 more genes
    nsv6636254copy number variation1nstd102humanUncertain significance GRCh37 chr4: 164,980,534-166,223,066 , GRCh38.p12 chr4: 164,059,382-165,301,914 ANP32CP, GK3, 24 more genes
    nsv6634351copy number variation1nstd102humanPathogenic GRCh37 chr4: 159,174,483-190,957,473 , GRCh38.p12 chr4: 158,253,331-190,036,318 COPS3P1, LOC339975, 363 more genes
    nsv6629627copy number variation1nstd224human GRCh37 chr4: 165,836,060-166,110,819 , GRCh38.p12 chr4: 164,914,908-165,189,667 NACA3P, LOC391711, 13 more genes
    nsv6556007inversion1nstd223human GRCh38 chr4: 165,093,991-165,094,723 , GRCh37.p13 chr4: 166,015,143-166,015,875 TMEM192
    nsv6391412copy number variation1nstd223human GRCh38 chr4: 165,081,465-165,083,903 , GRCh37.p13 chr4: 166,002,617-166,005,055 TMEM192
    nsv6383201copy number variation1nstd223human GRCh38 chr4: 165,093,375-165,094,290 , GRCh37.p13 chr4: 166,014,527-166,015,442 TMEM192
    nsv6382663copy number variation1nstd223human GRCh38 chr4: 165,090,188-165,094,967 , GRCh37.p13 chr4: 166,011,340-166,016,119 TMEM192
    nsv6376685copy number variation1nstd223human GRCh38 chr4: 165,098,313-165,099,108 , GRCh37.p13 chr4: 166,019,465-166,020,260 TMEM192
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