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Items: 1 to 20 of 405

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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
    nsv7138366copy number variation1nstd232human GRCh37.p13 chr4: 6,580,736-6,580,825 , GRCh38.p12 chr4: 6,579,009-6,579,098 MAN2B2
    nsv7137196copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-34,512,694 , GRCh38.p12 chr4: 68,453-34,511,072 ECM1P2, LOC105378240, 482 more genes
    nsv7057432inversion1nstd229human GRCh38 chr4: 4,018,387-9,499,063 , GRCh37.p13 chr4: 4,020,114-9,500,707 CPZ, OR7E85P, 127 more genes
    nsv7056110inversion1nstd229human GRCh38 chr4: 3,991,106-9,653,685 , GRCh37.p13 chr4: 3,992,833-9,655,309 MAN2B2, SH3TC1, 134 more genes
    nsv7050522inversion1nstd229human GRCh38 chr4: 4,174,346-12,367,773 , GRCh37.p13 chr4: 4,176,073-12,369,397 USP17L29, MIR4274, 165 more genes
    nsv7044696inversion1nstd229human GRCh38 chr4: 3,996,444-9,648,382 , GRCh37.p13 chr4: 3,998,171-9,650,006 EVC, USP17L18, 134 more genes
    nsv7039148inversion1nstd229human GRCh38 chr4: 4,150,240-8,956,846 , GRCh37.p13 chr4: 4,151,967-8,958,572 PPP2R2C, CRMP1, 80 more genes
    nsv7038223inversion1nstd229human GRCh38 chr4: 3,989,150-9,655,696 , GRCh37.p13 chr4: 3,990,877-9,657,320 RNA5SP152, MRFAP1, 134 more genes
    nsv6736196copy number variation1nstd229human GRCh38 chr4: 6,616,301-6,620,000 , GRCh37.p13 chr4: 6,618,028-6,621,727 MAN2B2
    nsv6735267copy number variation1nstd229human GRCh38 chr4: 6,579,107-6,586,570 , GRCh37.p13 chr4: 6,580,834-6,588,297 MAN2B2
    nsv6734091copy number variation1nstd229human GRCh38 chr4: 6,532,746-7,719,355 , GRCh37.p13 chr4: 6,534,473-7,721,082 MRFAP1, TADA2B, 27 more genes
    nsv6730353copy number variation1nstd229human GRCh38 chr4: 6,616,101-6,620,100 , GRCh37.p13 chr4: 6,617,828-6,621,827 MAN2B2
    nsv6728543copy number variation1nstd229human GRCh38 chr4: 6,592,873-6,611,426 , GRCh37.p13 chr4: 6,594,600-6,613,153 MAN2B2
    nsv6727671copy number variation1nstd229human GRCh38 chr4: 6,622,747-6,624,962 , GRCh37.p13 chr4: 6,624,474-6,626,689 MAN2B2
    nsv6727508copy number variation1nstd229human GRCh38 chr4: 5,958,577-6,585,601 , GRCh37.p13 chr4: 5,960,304-6,587,328 C4orf50, WFS1, 5 more genes
    nsv6723836copy number variation1nstd229human GRCh38 chr4: 6,610,366-6,616,637 , GRCh37.p13 chr4: 6,612,093-6,618,364 MAN2B2
    nsv6723208copy number variation1nstd229human GRCh38 chr4: 5,355,032-14,502,279 , GRCh37.p13 chr4: 5,356,759-14,503,903 OR7E86P, LINC02447, 164 more genes
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