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Items: 1 to 20 of 268

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148229copy number variation1nstd102humanPathogenic GRCh38 chr4: 2,904,667-42,963,232 , GRCh37.p13 chr4: 2,906,394-42,965,249 LINC01587, RN7SKP82, 509 more genes
    nsv7148161copy number variation1nstd102humanPathogenic GRCh38 chr4: 1-49,062,177 , GRCh37.p13 chr4: 507,005-49,064,194 SLIRPP2, STIM2-AS1, 659 more genes
    nsv7148157copy number variation1nstd102humanPathogenic GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396 OR7E84P, FAM193A, 764 more genes
    nsv7145604insertion1nstd232human GRCh37.p13 chr4: 24,542,573-24,542,573 , GRCh38.p12 chr4: 24,540,950-24,540,950 DHX15
    nsv7144177insertion1nstd232human GRCh37.p13 chr4: 24,572,472-24,572,472 , GRCh38.p12 chr4: 24,570,849-24,570,849 DHX15
    nsv7142609insertion1nstd232human GRCh37.p13 chr4: 24,558,033-24,558,033 , GRCh38.p12 chr4: 24,556,410-24,556,410 DHX15
    nsv7137196copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-34,512,694 , GRCh38.p12 chr4: 68,453-34,511,072 ECM1P2, LOC105378240, 482 more genes
    nsv7098818copy number variation1nstd102humanPathogenic GRCh38 chr4: 11,399,082-38,137,335 , GRCh37.p13 chr4: 11,400,706-38,138,956 LOC105374542, PPARGC1A, 232 more genes
    nsv7047237inversion1nstd229human GRCh38 chr4: 15,975,453-25,472,708 , GRCh37.p13 chr4: 15,977,076-25,474,330 LOC107986219, LOC102723675, 78 more genes
    nsv7045243inversion1nstd229human GRCh38 chr4: 24,518,332-25,683,739 , GRCh37.p13 chr4: 24,519,955-25,685,361 CCDC149, ATP5MGP3, 22 more genes
    nsv6737847copy number variation1nstd229human GRCh38 chr4: 24,409,942-24,692,090 , GRCh37.p13 chr4: 24,411,565-24,693,713 DHX15, LINC02473, 4 more genes
    nsv6736244copy number variation1nstd229human GRCh38 chr4: 24,440,186-24,558,403 , GRCh37.p13 chr4: 24,441,809-24,560,026 DHX15, PPARGC1A, 1 more genes
    nsv6725935copy number variation1nstd229human GRCh38 chr4: 24,415,319-24,565,940 , GRCh37.p13 chr4: 24,416,942-24,567,563 DHX15, PPARGC1A, 2 more genes
    nsv6721405copy number variation1nstd229human GRCh38 chr4: 24,558,201-24,563,400 , GRCh37.p13 chr4: 24,559,824-24,565,023 DHX15, RN7SL16P
    nsv6720351copy number variation1nstd229human GRCh38 chr4: 24,419,701-24,535,100 , GRCh37.p13 chr4: 24,421,324-24,536,723 PPARGC1A, DHX15, 1 more genes
    nsv6719128copy number variation1nstd229human GRCh38 chr4: 24,402,314-24,618,834 , GRCh37.p13 chr4: 24,403,937-24,620,457 PPARGC1A, DHX15, 2 more genes
    nsv6637075copy number variation1nstd102humanUncertain significance GRCh37 chr4: 16,249,194-24,864,955 , GRCh38.p12 chr4: 16,247,571-24,863,333 LOC107986262, QDPR, 63 more genes
    nsv6634358copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-49,089,361 , GRCh38.p12 chr4: 68,453-49,087,344 LINC02475, LOC105374344, 658 more genes
    nsv6629476copy number variation1nstd224human GRCh37 chr4: 24,584,445-24,706,382 , GRCh38.p12 chr4: 24,582,822-24,704,759 DHX15, ATP5MGP3, 1 more genes
    nsv6574397inversion1nstd223human GRCh38 chr4: 24,530,422-24,531,182 , GRCh37.p13 chr4: 24,532,045-24,532,805 DHX15
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