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Items: 1 to 20 of 288

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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
    nsv7143121insertion1nstd232human GRCh37.p13 chr4: 7,754,687-7,754,687 , GRCh38.p12 chr4: 7,752,960-7,752,960 AFAP1-AS1
    nsv7139439copy number variation1nstd232human GRCh37.p13 chr4: 7,768,257-7,768,326 , GRCh38.p12 chr4: 7,766,530-7,766,599 AFAP1, AFAP1-AS1
    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
    nsv7055699inversion1nstd229human GRCh38 chr4: 7,177,879-7,980,235 , GRCh37.p13 chr4: 7,179,606-7,981,962 LOC105374371, SORCS2, 8 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
    nsv6737127copy number variation1nstd229human GRCh38 chr4: 7,743,968-7,896,899 , GRCh37.p13 chr4: 7,745,695-7,898,626 AFAP1-AS1, AFAP1
    nsv6733983copy number variation1nstd229human GRCh38 chr4: 7,326,226-7,824,663 , GRCh37.p13 chr4: 7,327,953-7,826,390 AFAP1, SORCS2, 3 more genes
    nsv6733105copy number variation1nstd229human GRCh38 chr4: 7,586,316-7,837,522 , GRCh37.p13 chr4: 7,588,043-7,839,249 SORCS2, AFAP1, 1 more genes
    nsv6727957copy number variation1nstd229human GRCh38 chr4: 7,767,810-7,768,192 , GRCh37.p13 chr4: 7,769,537-7,769,919 AFAP1, AFAP1-AS1
    nsv6727546copy number variation1nstd229human GRCh38 chr4: 7,476,106-7,909,357 , GRCh37.p13 chr4: 7,477,833-7,911,084 SORCS2, AFAP1-AS1, 1 more genes
    nsv6726202copy number variation1nstd229human GRCh38 chr4: 7,699,701-7,855,700 , GRCh37.p13 chr4: 7,701,428-7,857,427 AFAP1, AFAP1-AS1, 1 more genes
    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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