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Items: 1 to 20 of 624

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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
    nsv7097006copy number variation1nstd102humanUncertain significance GRCh37 chr4: 8,869,419-10,118,290 , GRCh38.p12 chr4: 8,867,693-10,116,666 RNA5SP153, USP17L29, 59 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
    nsv7055114inversion1nstd229human GRCh38 chr4: 8,400,925-10,237,375 , GRCh37.p13 chr4: 8,402,652-10,238,999 LOC101928948, SLC2A9-AS1, 65 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
    nsv7040714inversion1nstd229human GRCh38 chr4: 8,676,530-9,855,545 , GRCh37.p13 chr4: 8,678,256-9,857,169 LOC101928948, UNC93B8, 56 more genes
    nsv7040297inversion1nstd229human GRCh38 chr4: 9,427,948-9,546,060 , GRCh37.p13 chr4: 9,429,674-9,547,685 OR7E84P, UNC93B7, 6 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
    nsv6729747copy number variation1nstd229human GRCh38 chr4: 9,447,572-9,460,796 , GRCh37.p13 chr4: 9,449,298-9,462,522 OR7E86P, DEFB131A
    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
    nsv6718881copy number variation1nstd229human GRCh38 chr4: 3,908,216-9,748,640 , GRCh37.p13 chr4: 3,909,943-9,750,264 USP17L21, CYTL1, 143 more genes
    nsv6636582copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,346-12,369,983 , GRCh38.p12 chr4: 68,454-12,368,359 NELFA, OR7E111FP, 289 more genes
    nsv6636256copy number variation1nstd102humanPathogenic GRCh37 chr4: 1-12,785,001 , GRCh38.p12 chr4: 10,001-12,783,377 AFAP1-AS1, LOC389199, 294 more genes
    nsv6634909copy number variation1nstd227human GRCh38.p12 chr4: 9,369,390-9,455,251 , GRCh37 chr4: 9,371,116-9,456,977 USP17L6P, DEFB131A, 4 more genes
    nsv6634358copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-49,089,361 , GRCh38.p12 chr4: 68,453-49,087,344 LINC02475, LOC105374344, 658 more genes
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