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Items: 1 to 20 of 438

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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
    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
    nsv7096726copy number variation2nstd102humanUncertain significance GRCh37 chr4: 15,477,557-16,228,080 , GRCh38.p12 chr4: 15,475,933-16,226,457 LOC107986187, CC2D2A, 15 more genes
    nsv7044543inversion1nstd229human GRCh38 chr4: 15,624,859-15,624,881 , GRCh37.p13 chr4: 15,626,482-15,626,504 FBXL5
    nsv6737822copy number variation1nstd229human GRCh38 chr4: 15,631,001-15,632,800 , GRCh37.p13 chr4: 15,632,624-15,634,423 FBXL5
    nsv6735836copy number variation1nstd229human GRCh38 chr4: 15,650,419-15,652,295 , GRCh37.p13 chr4: 15,652,042-15,653,918 FBXL5, FAM200B
    nsv6735328copy number variation1nstd229human GRCh38 chr4: 15,662,167-15,662,266 , GRCh37.p13 chr4: 15,663,790-15,663,889 FBXL5, FAM200B
    nsv6734448copy number variation1nstd229human GRCh38 chr4: 15,619,373-15,682,394 , GRCh37.p13 chr4: 15,620,996-15,684,017 FBXL5, FAM200B
    nsv6733409copy number variation1nstd229human GRCh38 chr4: 15,636,678-15,638,510 , GRCh37.p13 chr4: 15,638,301-15,640,133 FBXL5
    nsv6730220copy number variation1nstd229human GRCh38 chr4: 15,628,034-15,630,667 , GRCh37.p13 chr4: 15,629,657-15,632,290 FBXL5
    nsv6730100copy number variation1nstd229human GRCh38 chr4: 15,662,600-15,672,684 , GRCh37.p13 chr4: 15,664,223-15,674,307 FBXL5, FAM200B
    nsv6729853copy number variation1nstd229human GRCh38 chr4: 15,673,783-15,675,638 , GRCh37.p13 chr4: 15,675,406-15,677,261 FBXL5, FAM200B
    nsv6729439copy number variation1nstd229human GRCh38 chr4: 15,605,800-15,612,263 , GRCh37.p13 chr4: 15,607,423-15,613,886 FBXL5
    nsv6729345copy number variation1nstd229human GRCh38 chr4: 15,616,452-15,616,826 , GRCh37.p13 chr4: 15,618,075-15,618,449 FBXL5
    nsv6728090copy number variation1nstd229human GRCh38 chr4: 15,643,831-15,643,982 , GRCh37.p13 chr4: 15,645,454-15,645,605 FBXL5
    nsv6725960copy number variation1nstd229human GRCh38 chr4: 15,636,463-15,636,669 , GRCh37.p13 chr4: 15,638,086-15,638,292 FBXL5
    nsv6723056copy number variation1nstd229human GRCh38 chr4: 15,640,601-15,745,400 , GRCh37.p13 chr4: 15,642,224-15,747,023 FAM200B, RPL10AP7, 3 more genes
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