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Items: 1 to 20 of 173

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5907258copy number variation1nstd209human GRCh38 chr4: 87,165,110-92,683,258 , GRCh37.p13 chr4: 88,086,262-93,604,409 HSP90AB3P, SPP1, 61 more genes
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5547030insertion1nstd206human GRCh38 chr4: 68,996,170-113,894,177 , GRCh37.p13 chr4: 69,861,888-114,815,333 , MIR548AH, 616 more genes
    nsv5095318mobile element insertion1nstd203human GRCh38 chr4: 88,274,678-88,274,693 , GRCh37.p13 chr4: 89,195,830-89,195,845 RNU6-112P, PPM1K
    nsv5040446inversion1nstd200human GRCh38 chr4: 76,223,829-89,968,114 , GRCh37.p13 chr4: 77,144,982-90,889,265 , KPNA2P1, 209 more genes
    nsv5034204inversion1nstd200human GRCh38 chr4: 45,103,677-117,623,076 , GRCh37.p13 chr4: 45,105,694-118,544,231 , LOC100129728, 913 more genes
    nsv4925891copy number variation1nstd200human GRCh38 chr4: 88,251,803-88,314,970 , GRCh37.p13 chr4: 89,172,955-89,236,122 RNU6-112P, PPM1K, 1 more genes
    nsv4923457copy number variation1nstd200human GRCh38 chr4: 88,252,596-88,258,524 , GRCh37.p13 chr4: 89,173,748-89,179,676 PPM1K
    nsv4878267inversion1nstd200human GRCh37 chr4: 45,105,694-118,544,231 , GRCh38.p12 chr4: 45,103,677-117,623,076 , MIR367, 913 more genes
    nsv4809367copy number variation1nstd200human GRCh37 chr4: 89,172,951-89,236,137 , GRCh38.p12 chr4: 88,251,799-88,314,985 PPM1K-DT, RNU6-112P, 1 more genes
    nsv4800547copy number variation1nstd200human GRCh37 chr4: 89,173,748-89,179,676 , GRCh38.p12 chr4: 88,252,596-88,258,524 PPM1K
    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
    nsv4739281copy number variation1nstd199human GRCh37 chr4: 89,187,628-89,187,786 , GRCh38.p12 chr4: 88,266,476-88,266,634 PPM1K
    nsv4729814copy number variation1nstd102humanPathogenic GRCh38 chr4: 88,268,907-90,128,499 , GRCh37.p13 chr4: 89,190,059-91,049,650 SNCA-AS1, LOC102723458, 27 more genes
    nsv4714757copy number variation1nstd195human GRCh37 chr4: 89,180,501-89,233,201 , GRCh38.p12 chr4: 88,259,349-88,312,049 PPM1K, PPM1K-DT, 1 more genes
    nsv4709652copy number variation1nstd195human GRCh38.p12 chr4: 88,161,849-88,259,299 , GRCh37 chr4: 89,083,001-89,180,451 ABCG2, PPM1K, 4 more genes
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