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Items: 1 to 20 of 988

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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
    nsv7143408insertion1nstd232human GRCh37.p13 chr4: 20,937,545-20,937,545 , GRCh38.p12 chr4: 20,935,922-20,935,922 KCNIP4
    nsv7142161insertion1nstd232human GRCh37.p13 chr4: 21,161,005-21,161,005 , GRCh38.p12 chr4: 21,159,382-21,159,382 KCNIP4
    nsv7140164insertion1nstd232human GRCh37.p13 chr4: 21,323,342-21,323,342 , GRCh38.p12 chr4: 21,321,719-21,321,719 KCNIP4
    nsv7139633copy number variation1nstd232human GRCh37.p13 chr4: 21,758,749-21,758,820 , GRCh38.p12 chr4: 21,757,126-21,757,197 KCNIP4
    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
    nsv7057819inversion1nstd229human GRCh38 chr4: 21,128,302-21,137,113 , GRCh37.p13 chr4: 21,129,925-21,138,736 KCNIP4
    nsv7057488inversion1nstd229human GRCh38 chr4: 21,627,918-21,644,243 , GRCh37.p13 chr4: 21,629,541-21,645,866 KCNIP4
    nsv7057454inversion1nstd229human GRCh38 chr4: 21,800,403-21,821,305 , GRCh37.p13 chr4: 21,802,026-21,822,928 KCNIP4
    nsv7057393inversion1nstd229human GRCh38 chr4: 21,527,082-21,527,227 , GRCh37.p13 chr4: 21,528,705-21,528,850 KCNIP4
    nsv7054404inversion1nstd229human GRCh38 chr4: 21,527,212-21,527,319 , GRCh37.p13 chr4: 21,528,835-21,528,942 KCNIP4
    nsv7052144inversion1nstd229human GRCh38 chr4: 20,789,188-20,789,257 , GRCh37.p13 chr4: 20,790,811-20,790,880 KCNIP4
    nsv7052062inversion1nstd229human GRCh38 chr4: 21,644,238-21,657,135 , GRCh37.p13 chr4: 21,645,861-21,658,758 KCNIP4, RPL31P25
    nsv7050887inversion1nstd229human GRCh38 chr4: 21,803,666-21,803,745 , GRCh37.p13 chr4: 21,805,289-21,805,368 KCNIP4
    nsv7050846inversion1nstd229human GRCh38 chr4: 21,911,827-21,915,018 , GRCh37.p13 chr4: 21,913,450-21,916,641 KCNIP4
    nsv7047237inversion1nstd229human GRCh38 chr4: 15,975,453-25,472,708 , GRCh37.p13 chr4: 15,977,076-25,474,330 LOC107986219, LOC102723675, 78 more genes
    nsv7047196inversion1nstd229human GRCh38 chr4: 21,636,961-21,643,548 , GRCh37.p13 chr4: 21,638,584-21,645,171 KCNIP4
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