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Items: 1 to 20 of 115

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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
    nsv7041145inversion1nstd229human GRCh38 chr4: 36,063,907-36,070,463 , GRCh37.p13 chr4: 36,065,529-36,072,085 ARAP2, LOC651644
    nsv6737657copy number variation1nstd229human GRCh38 chr4: 35,877,171-36,151,716 , GRCh37.p13 chr4: 35,878,793-36,153,338 LOC105374397, ARAP2, 1 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
    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
    nsv6728644copy number variation1nstd229human GRCh38 chr4: 35,864,624-36,065,403 , GRCh37.p13 chr4: 35,866,246-36,067,025 LOC105374396, LOC105374397, 2 more genes
    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
    nsv6634739copy number variation1nstd227human GRCh38.p12 chr4: 35,858,331-36,066,664 , GRCh37 chr4: 35,859,953-36,068,286 ARAP2, LOC651644, 2 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
    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
    nsv6364694copy number variation1nstd223human GRCh38 chr4: 36,064,401-36,065,800 , GRCh37.p13 chr4: 36,066,023-36,067,422 ARAP2, LOC651644
    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
    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
    nsv5315327copy number variation1nstd204human GRCh38.p13 chr4: 35,864,621-36,065,407 , GRCh37.p13 chr4: 35,866,243-36,067,029 LOC105374396, LOC105374397, 2 more genes
    nsv5224843copy number variation1nstd204human GRCh38.p13 chr4: 35,965,301-36,065,400 , GRCh37.p13 chr4: 35,966,923-36,067,022 LOC105374397, LOC651644, 1 more genes
    nsv5223783copy number variation1nstd204human GRCh38.p13 chr4: 35,864,601-36,064,000 , GRCh37.p13 chr4: 35,866,223-36,065,622 LOC105374397, LOC651644, 2 more genes
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