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Items: 1 to 20 of 327

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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
    nsv7140085copy number variation1nstd232human GRCh37.p13 chr4: 2,947,887-2,947,971 , GRCh38.p12 chr4: 2,946,160-2,946,244 NOP14, NOP14-AS1
    nsv7137196copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-34,512,694 , GRCh38.p12 chr4: 68,453-34,511,072 ECM1P2, LOC105378240, 482 more genes
    nsv7049289inversion1nstd229human GRCh38 chr4: 1,879,237-2,966,412 , GRCh37.p13 chr4: 1,880,964-2,968,139 RNF4, SCARNA22, 28 more genes
    nsv7043144inversion1nstd229human GRCh38 chr4: 2,884,197-3,271,248 , GRCh37.p13 chr4: 2,885,924-3,272,975 HTT, NOP14, 8 more genes
    nsv7040457inversion1nstd229human GRCh38 chr4: 2,747,436-3,221,045 , GRCh37.p13 chr4: 2,749,163-3,222,772 HTT, NOP14-AS1, 10 more genes
    nsv7039441inversion1nstd229human GRCh38 chr4: 1,689,472-2,959,448 , GRCh37.p13 chr4: 1,691,199-2,961,175 NOP14-AS1, LOC112268460, 34 more genes
    nsv6736472copy number variation1nstd229human GRCh38 chr4: 2,943,830-2,949,023 , GRCh37.p13 chr4: 2,945,557-2,950,750 NOP14-AS1, NOP14
    nsv6735535copy number variation1nstd229human GRCh38 chr4: 2,903,490-3,202,303 , GRCh37.p13 chr4: 2,905,217-3,204,030 MFSD10, GRK4, 7 more genes
    nsv6735145copy number variation1nstd229human GRCh38 chr4: 2,879,132-2,943,025 , GRCh37.p13 chr4: 2,880,859-2,944,752 NOP14-AS1, MFSD10, 2 more genes
    nsv6728207copy number variation1nstd229human GRCh38 chr4: 2,945,281-2,952,126 , GRCh37.p13 chr4: 2,947,008-2,953,853 NOP14-AS1, NOP14
    nsv6728099copy number variation1nstd229human GRCh38 chr4: 2,936,520-2,941,719 , GRCh37.p13 chr4: 2,938,247-2,943,446 NOP14-AS1, NOP14
    nsv6723730copy number variation1nstd229human GRCh38 chr4: 2,940,958-2,941,108 , GRCh37.p13 chr4: 2,942,685-2,942,835 NOP14, NOP14-AS1
    nsv6636582copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,346-12,369,983 , GRCh38.p12 chr4: 68,454-12,368,359 NELFA, OR7E111FP, 289 more genes
    nsv6636417copy number variation1nstd102humanUncertain significance GRCh37 chr4: 2,906,453-3,225,478 , GRCh38.p12 chr4: 2,904,726-3,223,751 GRK4, MFSD10, 7 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
    nsv6634358copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-49,089,361 , GRCh38.p12 chr4: 68,453-49,087,344 LINC02475, LOC105374344, 658 more genes
    nsv6372296copy number variation1nstd223human GRCh38 chr4: 2,940,424-3,030,121 , GRCh37.p13 chr4: 2,942,151-3,031,848 NOP14, GRK4, 1 more genes
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