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Items: 1 to 20 of 694

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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
    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
    nsv7055362inversion1nstd229human GRCh38 chr4: 26,793,374-26,793,713 , GRCh37.p13 chr4: 26,794,996-26,795,335 TBC1D19
    nsv7051717inversion1nstd229human GRCh38 chr4: 26,813,907-26,846,399 , GRCh37.p13 chr4: 26,815,529-26,848,021 TBC1D19
    nsv7041988inversion1nstd229human GRCh38 chr4: 26,693,878-27,160,863 , GRCh37.p13 chr4: 26,695,500-27,162,485 STIM2, STIM2-AS1, 2 more genes
    nsv6737880copy number variation1nstd229human GRCh38 chr4: 26,632,401-26,634,600 , GRCh37.p13 chr4: 26,634,023-26,636,222 TBC1D19
    nsv6737850copy number variation1nstd229human GRCh38 chr4: 26,783,357-26,783,999 , GRCh37.p13 chr4: 26,784,979-26,785,621 TBC1D19
    nsv6736216copy number variation1nstd229human GRCh38 chr4: 26,793,277-26,796,837 , GRCh37.p13 chr4: 26,794,899-26,798,459 TBC1D19
    nsv6735143copy number variation1nstd229human GRCh38 chr4: 26,831,301-26,834,700 , GRCh37.p13 chr4: 26,832,923-26,836,322 TBC1D19
    nsv6734232copy number variation1nstd229human GRCh38 chr4: 26,691,077-26,743,053 , GRCh37.p13 chr4: 26,692,699-26,744,675 TBC1D19
    nsv6734049copy number variation1nstd229human GRCh38 chr4: 26,781,292-26,781,343 , GRCh37.p13 chr4: 26,782,914-26,782,965 TBC1D19
    nsv6733732copy number variation1nstd229human GRCh38 chr4: 26,636,401-26,659,200 , GRCh37.p13 chr4: 26,638,023-26,660,822 TBC1D19
    nsv6732861copy number variation1nstd229human GRCh38 chr4: 26,829,397-26,829,756 , GRCh37.p13 chr4: 26,831,019-26,831,378 TBC1D19
    nsv6732477copy number variation1nstd229human GRCh38 chr4: 26,820,470-26,825,580 , GRCh37.p13 chr4: 26,822,092-26,827,202 TBC1D19
    nsv6732128copy number variation1nstd229human GRCh38 chr4: 26,636,301-26,648,100 , GRCh37.p13 chr4: 26,637,923-26,649,722 TBC1D19
    nsv6731963copy number variation1nstd229human GRCh38 chr4: 26,679,315-26,679,658 , GRCh37.p13 chr4: 26,680,937-26,681,280 TBC1D19
    nsv6729789copy number variation1nstd229human GRCh38 chr4: 26,807,738-26,807,781 , GRCh37.p13 chr4: 26,809,360-26,809,403 TBC1D19
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