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Items: 1 to 20 of 1404

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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
    nsv7137048copy number variation1nstd102humanPathogenic GRCh37 chr4: 40,337,485-41,941,400 , GRCh38.p12 chr4: 40,335,468-41,939,383 RNU6-1195P, RNU6-836P, 23 more genes
    nsv7057597inversion1nstd229human GRCh38 chr4: 40,706,162-41,294,144 , GRCh37.p13 chr4: 40,708,179-41,296,161 UCHL1-DT, UCHL1, 6 more genes
    nsv7055239inversion1nstd229human GRCh38 chr4: 40,146,946-41,050,224 , GRCh37.p13 chr4: 40,148,566-41,052,241 RHOH, RBM47, 10 more genes
    nsv7054319inversion1nstd229human GRCh38 chr4: 40,437,339-43,087,585 , GRCh37.p13 chr4: 40,439,356-43,089,602 RN7SKP82, RPS7P7, 33 more genes
    nsv7049429inversion1nstd229human GRCh38 chr4: 40,815,620-40,817,747 , GRCh37.p13 chr4: 40,817,637-40,819,764 APBB2, NSUN7
    nsv7045750inversion1nstd229human GRCh38 chr4: 41,031,168-41,109,767 , GRCh37.p13 chr4: 41,033,185-41,111,784 APBB2, RNU6-836P
    nsv7044695inversion1nstd229human GRCh38 chr4: 40,916,759-40,930,070 , GRCh37.p13 chr4: 40,918,776-40,932,087 APBB2
    nsv7041873inversion1nstd229human GRCh38 chr4: 40,939,479-40,939,560 , GRCh37.p13 chr4: 40,941,496-40,941,577 APBB2
    nsv6738068copy number variation1nstd229human GRCh38 chr4: 41,170,839-41,177,428 , GRCh37.p13 chr4: 41,172,856-41,179,445 APBB2
    nsv6737971copy number variation1nstd229human GRCh38 chr4: 40,836,569-40,836,604 , GRCh37.p13 chr4: 40,838,586-40,838,621 APBB2
    nsv6737955copy number variation1nstd229human GRCh38 chr4: 40,799,001-40,811,900 , GRCh37.p13 chr4: 40,801,018-40,813,917 APBB2, NSUN7
    nsv6737897copy number variation1nstd229human GRCh38 chr4: 40,950,886-40,951,731 , GRCh37.p13 chr4: 40,952,903-40,953,748 APBB2
    nsv6737713copy number variation1nstd229human GRCh38 chr4: 40,988,329-40,991,579 , GRCh37.p13 chr4: 40,990,346-40,993,596 RNA5SP160, APBB2
    nsv6737705copy number variation1nstd229human GRCh38 chr4: 41,058,594-41,066,319 , GRCh37.p13 chr4: 41,060,611-41,068,336 APBB2
    nsv6736906copy number variation1nstd229human GRCh38 chr4: 40,807,101-40,848,400 , GRCh37.p13 chr4: 40,809,118-40,850,417 NSUN7, APBB2
    nsv6736510copy number variation1nstd229human GRCh38 chr4: 40,950,151-40,952,419 , GRCh37.p13 chr4: 40,952,168-40,954,436 APBB2
    nsv6736281copy number variation1nstd229human GRCh38 chr4: 40,878,048-40,878,116 , GRCh37.p13 chr4: 40,880,065-40,880,133 APBB2
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