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Items: 1 to 20 of 208

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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
    nsv7048640inversion1nstd229human GRCh38 chr4: 13,649,014-14,982,273 , GRCh37.p13 chr4: 13,650,638-14,983,897 C9orf78P2, LOC107986182, 9 more genes
    nsv7044725inversion1nstd229human GRCh38 chr4: 14,031,306-14,396,800 , GRCh37.p13 chr4: 14,032,930-14,398,424 LINC01085, KLF17P2
    nsv6735847copy number variation1nstd229human GRCh38 chr4: 14,119,798-14,120,044 , GRCh37.p13 chr4: 14,121,422-14,121,668 LINC01085
    nsv6732009copy number variation1nstd229human GRCh38 chr4: 13,174,270-14,155,070 , GRCh37.p13 chr4: 13,175,894-14,156,694 LOC101929048, HSP90AB2P, 14 more genes
    nsv6727829copy number variation1nstd229human GRCh38 chr4: 14,108,601-14,111,800 , GRCh37.p13 chr4: 14,110,225-14,113,424 LINC01085
    nsv6726750copy number variation1nstd229human GRCh38 chr4: 14,100,606-14,200,269 , GRCh37.p13 chr4: 14,102,230-14,201,893 LINC01085, KLF17P2
    nsv6725269copy number variation1nstd229human GRCh38 chr4: 13,702,660-14,142,258 , GRCh37.p13 chr4: 13,704,284-14,143,882 LINC01085, KLF17P2, 4 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
    nsv6723049copy number variation1nstd229human GRCh38 chr4: 14,115,009-14,187,474 , GRCh37.p13 chr4: 14,116,633-14,189,098 LINC01085, KLF17P2
    nsv6719490copy number variation1nstd229human GRCh38 chr4: 13,830,545-14,119,063 , GRCh37.p13 chr4: 13,832,169-14,120,687 LOC107986182, LINC01085, 3 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
    nsv6373244copy number variation1nstd223human GRCh38 chr4: 14,108,599-14,111,770 , GRCh37.p13 chr4: 14,110,223-14,113,394 LINC01085
    nsv6369876copy number variation1nstd223human GRCh38 chr4: 14,134,101-14,140,000 , GRCh37.p13 chr4: 14,135,725-14,141,624 LINC01085
    nsv6369783copy number variation1nstd223human GRCh38 chr4: 14,100,606-14,200,268 , GRCh37.p13 chr4: 14,102,230-14,201,892 KLF17P2, LINC01085
    nsv6369340copy number variation1nstd223human GRCh38 chr4: 14,117,587-14,118,444 , GRCh37.p13 chr4: 14,119,211-14,120,068 LINC01085
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