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Items: 1 to 20 of 294

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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
    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
    nsv7097247copy number variation1nstd102humanUncertain significance GRCh37 chr4: 36,345,104-36,345,446 , GRCh38.p12 chr4: 36,343,482-36,343,824 DTHD1
    nsv7096729copy number variation1nstd102humanUncertain significance GRCh37 chr4: 36,317,844-36,318,128 , GRCh38.p12 chr4: 36,316,222-36,316,506 DTHD1
    nsv6737918copy number variation1nstd229human GRCh38 chr4: 36,264,155-36,306,664 , GRCh37.p13 chr4: 36,265,777-36,308,286 LOC439933, DTHD1
    nsv6737446copy number variation1nstd229human GRCh38 chr4: 33,221,950-37,299,602 , GRCh37.p13 chr4: 33,223,572-37,301,224 LOC100130532, LOC107986272, 24 more genes
    nsv6736323copy number variation1nstd229human GRCh38 chr4: 36,308,677-36,313,358 , GRCh37.p13 chr4: 36,310,299-36,314,980 DTHD1
    nsv6735517copy number variation1nstd229human GRCh38 chr4: 36,121,807-36,447,572 , GRCh37.p13 chr4: 36,123,429-36,449,194 ARAP2, MIR1255B1, 3 more genes
    nsv6734198copy number variation1nstd229human GRCh38 chr4: 35,669,623-36,406,945 , GRCh37.p13 chr4: 35,671,245-36,408,567 LOC439933, LOC651644, 5 more genes
    nsv6732814copy number variation1nstd229human GRCh38 chr4: 36,290,720-36,292,024 , GRCh37.p13 chr4: 36,292,342-36,293,646 DTHD1
    nsv6730111copy number variation1nstd229human GRCh38 chr4: 36,306,878-36,322,439 , GRCh37.p13 chr4: 36,308,500-36,324,061 DTHD1
    nsv6727581copy number variation1nstd229human GRCh38 chr4: 28,550,139-38,411,880 , GRCh37.p13 chr4: 28,551,761-38,413,501 LINC02497, MESTP3, 66 more genes
    nsv6727334copy number variation1nstd229human GRCh38 chr4: 36,332,214-36,332,260 , GRCh37.p13 chr4: 36,333,836-36,333,882 DTHD1
    nsv6726072copy number variation1nstd229human GRCh38 chr4: 36,347,393-36,350,489 , GRCh37.p13 chr4: 36,349,015-36,352,111 DTHD1
    nsv6721455copy number variation1nstd229human GRCh38 chr4: 36,306,601-36,328,300 , GRCh37.p13 chr4: 36,308,223-36,329,922 DTHD1
    nsv6721442copy number variation1nstd229human GRCh38 chr4: 36,308,241-36,308,407 , GRCh37.p13 chr4: 36,309,863-36,310,029 DTHD1
    nsv6719750copy number variation1nstd229human GRCh38 chr4: 36,268,994-36,287,476 , GRCh37.p13 chr4: 36,270,616-36,289,098 LOC439933, DTHD1
    nsv6718211copy number variation1nstd229human GRCh38 chr4: 36,321,812-36,325,931 , GRCh37.p13 chr4: 36,323,434-36,327,553 DTHD1
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