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Items: 1 to 20 of 107

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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
    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
    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
    nsv6732651copy number variation1nstd229human GRCh38 chr4: 36,382,657-36,629,775 , GRCh37.p13 chr4: 36,384,279-36,631,397 LINC02505, MIR1255B1, 1 more genes
    nsv6727910copy number variation1nstd229human GRCh38 chr4: 36,426,121-36,426,269 , GRCh37.p13 chr4: 36,427,743-36,427,891 MIR1255B1
    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
    nsv6720170copy number variation1nstd229human GRCh38 chr4: 36,389,405-36,434,431 , GRCh37.p13 chr4: 36,391,027-36,436,053 MIR1255B1
    nsv6718710copy number variation1nstd229human GRCh38 chr4: 36,417,998-36,521,964 , GRCh37.p13 chr4: 36,419,620-36,523,586 LOC100130532, MIR1255B1, 1 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
    nsv6315440copy number variation1nstd102humanPathogenic GRCh37 chr4: 114,784-47,569,569 , GRCh38.p12 chr4: 114,902-47,567,552 FAM86KP, ENPP7P11, 631 more genes
    nsv6313559copy number variation1nstd102humanPathogenic GRCh37 chr4: 19,892,850-37,325,128 , GRCh38.p12 chr4: 19,891,227-37,323,506 LOC102723846, KCNIP4-IT1, 135 more genes
    nsv6297170copy number variation1nstd186human GRCh37 chr4: 36,112,961-36,505,492 , GRCh38.p12 chr4: 36,111,339-36,503,870 ARAP2, DTHD1, 4 more genes
    nsv6135335copy number variation1nstd213human GRCh37 chr4: 36,070,000-36,550,001 , GRCh38.p12 chr4: 36,068,378-36,548,379 ARAP2, DTHD1, 5 more genes
    nsv6135334copy number variation1nstd213human GRCh37 chr4: 35,190,000-37,140,001 , GRCh38.p12 chr4: 35,188,378-37,138,379 ARAP2, DTHD1, 13 more genes
    nsv5459508copy number variation1nstd206human GRCh38 chr4: 36,111,339-36,503,870 , GRCh37.p13 chr4: 36,112,961-36,505,492 ARAP2, DTHD1, 4 more genes
    nsv5039232inversion1nstd200human GRCh38 chr4: 9,660,225-57,055,279 , GRCh37.p13 chr4: 9,661,849-57,921,445 , KRT18P63, 533 more genes
    nsv4761770inversion1nstd199human GRCh37 chr4: 34,988-191,015,248 , GRCh38.p12 chr4: 34,988-190,094,093 , ADD1, 2433 more genes
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