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Items: 1 to 20 of 186

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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
    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
    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
    nsv6729233copy number variation1nstd229human GRCh38 chr4: 36,242,020-36,242,234 , GRCh37.p13 chr4: 36,243,642-36,243,856 LOC439933, ARAP2
    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
    nsv6725511copy number variation1nstd229human GRCh38 chr4: 36,242,001-36,270,400 , GRCh37.p13 chr4: 36,243,623-36,272,022 ARAP2, LOC439933
    nsv6722504copy number variation1nstd229human GRCh38 chr4: 36,244,701-36,248,900 , GRCh37.p13 chr4: 36,246,323-36,250,522 LOC439933, ARAP2
    nsv6719750copy number variation1nstd229human GRCh38 chr4: 36,268,994-36,287,476 , GRCh37.p13 chr4: 36,270,616-36,289,098 LOC439933, DTHD1
    nsv6634358copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-49,089,361 , GRCh38.p12 chr4: 68,453-49,087,344 LINC02475, LOC105374344, 658 more genes
    nsv6629680copy number variation1nstd224human GRCh37 chr4: 35,673,557-36,407,872 , GRCh38.p12 chr4: 35,671,935-36,406,250 ARAP2, DTHD1, 5 more genes
    nsv6565402inversion1nstd223human GRCh38 chr4: 36,246,096-36,247,158 , GRCh37.p13 chr4: 36,247,718-36,248,780 LOC439933
    nsv6363291copy number variation1nstd223human GRCh38 chr4: 36,244,701-36,248,800 , GRCh37.p13 chr4: 36,246,323-36,250,422 ARAP2, LOC439933
    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
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