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Items: 1 to 20 of 99

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5721577mobile element insertion1nstd211human GRCh38 chr4: 56,320,402-56,320,402 , GRCh37.p13 chr4: 57,186,568-57,186,568 CRACD, MRPL22P1
    nsv5674237copy number variation1nstd102humanPathogenic GRCh38 chr4: 51,891,814-76,009,719 , GRCh37.p13 chr4: 52,757,980-76,930,872 FTLP10, RNU6-410P, 335 more genes
    nsv5557875sequence alteration1nstd206human GRCh38 chr4: 56,179,761-56,589,194 , GRCh37.p13 chr4: 57,045,927-57,455,360 , PPAT, 12 more genes
    nsv5555750mobile element insertion1nstd206human GRCh38 chr4: 56,320,402-56,320,453 , GRCh37.p13 chr4: 57,186,568-57,186,619 CRACD, MRPL22P1
    nsv5039232inversion1nstd200human GRCh38 chr4: 9,660,225-57,055,279 , GRCh37.p13 chr4: 9,661,849-57,921,445 , KRT18P63, 533 more genes
    nsv5034204inversion1nstd200human GRCh38 chr4: 45,103,677-117,623,076 , GRCh37.p13 chr4: 45,105,694-118,544,231 , LOC100129728, 913 more genes
    nsv4928805copy number variation1nstd200human GRCh38 chr4: 56,213,754-56,393,163 , GRCh37.p13 chr4: 57,079,920-57,259,329 , PPAT, 7 more genes
    nsv4878267inversion1nstd200human GRCh37 chr4: 45,105,694-118,544,231 , GRCh38.p12 chr4: 45,103,677-117,623,076 , MIR367, 913 more genes
    nsv4761770inversion1nstd199human GRCh37 chr4: 34,988-191,015,248 , GRCh38.p12 chr4: 34,988-190,094,093 , ADD1, 2433 more genes
    nsv4758212inversion1nstd199human GRCh37 chr4: 30,775-191,019,445 , GRCh38.p12 chr4: 30,775-190,098,290 , ADD1, 2433 more genes
    nsv4754592inversion1nstd199human GRCh37 chr4: 27,111-191,020,337 , GRCh38.p12 chr4: 27,111-190,099,182 , ADD1, 2433 more genes
    nsv4753570inversion1nstd199human GRCh37 chr4: 19,034-191,028,414 , GRCh38.p12 chr4: 19,034-190,107,259 , ADD1, 2434 more genes
    nsv4751554inversion1nstd199human GRCh37 chr4: 18,939-191,034,785 , GRCh38.p12 chr4: 18,939-190,113,630 , ADD1, 2434 more genes
    nsv4673993copy number variation1nstd102humanUncertain significance GRCh37 chr4: 57,067,953-57,957,651 , GRCh38.p12 chr4: 56,201,787-57,091,485 LOC285453, PPAT, 27 more genes
    nsv4558011mobile element insertion1nstd166human GRCh37.p13 chr4: 57,186,553-57,186,553 , GRCh38.p12 chr4: 56,320,387-56,320,387 CRACD, MRPL22P1
    nsv4382322copy number variation1nstd173human GRCh37 chr4: 57,006,969-57,225,313 , GRCh38.p12 chr4: 56,140,803-56,359,147 , MRPL22P1, 6 more genes
    nsv4337678sequence alteration1nstd166human GRCh37.p13 chr4: 57,045,915-57,455,360 , GRCh38.p12 chr4: 56,179,749-56,589,194 , ARL9, 13 more genes
    nsv4337474sequence alteration1nstd166human GRCh37.p13 chr4: 57,101,147-57,380,044 , GRCh38.p12 chr4: 56,234,981-56,513,878 , CRACD, 11 more genes
    nsv4107273copy number variation1nstd166human GRCh37.p13 chr4: 56,828,561-57,670,971 , GRCh38.p12 chr4: 55,962,395-56,804,805 , GLDCP1, 24 more genes
    nsv4104127copy number variation1nstd166human GRCh37.p13 chr4: 57,006,969-57,295,947 , GRCh38.p12 chr4: 56,140,803-56,429,781 , LOC101928760, 8 more genes
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