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Items: 1 to 20 of 157

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7048744inversion1nstd229human GRCh38 chr4: 47,920,338-48,060,660 , GRCh37.p13 chr4: 47,922,355-48,062,677 CNGA1, NIPAL1, 1 more genes
    nsv6725842copy number variation1nstd229human GRCh38 chr4: 48,001,001-48,021,000 , GRCh37.p13 chr4: 48,003,018-48,023,017 CNGA1, NIPAL1
    nsv6720502copy number variation1nstd229human GRCh38 chr4: 48,031,639-48,032,643 , GRCh37.p13 chr4: 48,033,656-48,034,660 NIPAL1
    nsv6634358copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-49,089,361 , GRCh38.p12 chr4: 68,453-49,087,344 LINC02475, LOC105374344, 658 more genes
    nsv6559339inversion1nstd223human GRCh38 chr4: 48,025,454-48,026,175 , GRCh37.p13 chr4: 48,027,471-48,028,192 NIPAL1
    nsv6383147copy number variation1nstd223human GRCh38 chr4: 47,978,060-48,024,146 , GRCh37.p13 chr4: 47,980,077-48,026,163 LOC101927157, NIPAL1, 1 more genes
    nsv6376109copy number variation1nstd223human GRCh38 chr4: 48,032,031-48,039,728 , GRCh37.p13 chr4: 48,034,048-48,041,745 NIPAL1
    nsv6134938copy number variation1nstd213human GRCh37 chr4: 47,800,000-48,170,001 , GRCh38.p12 chr4: 47,797,983-48,167,984 CNGA1, TEC, 7 more genes
    nsv5088726mobile element insertion1nstd203human GRCh38 chr4: 48,023,817-48,023,834 , GRCh37.p13 chr4: 48,025,834-48,025,851 NIPAL1
    nsv5039232inversion1nstd200human GRCh38 chr4: 9,660,225-57,055,279 , GRCh37.p13 chr4: 9,661,849-57,921,445 , KRT18P63, 533 more genes
    nsv5034204inversion1nstd200human GRCh38 chr4: 45,103,677-117,623,076 , GRCh37.p13 chr4: 45,105,694-118,544,231 , LOC100129728, 913 more genes
    nsv4878267inversion1nstd200human GRCh37 chr4: 45,105,694-118,544,231 , GRCh38.p12 chr4: 45,103,677-117,623,076 , MIR367, 913 more genes
    nsv4791614copy number variation1nstd200human GRCh37 chr4: 43,358,175-53,119,711 , GRCh38.p12 chr4: 43,356,158-52,253,545 , LOC107986277, 78 more genes
    nsv4761770inversion1nstd199human GRCh37 chr4: 34,988-191,015,248 , GRCh38.p12 chr4: 34,988-190,094,093 , ADD1, 2433 more genes
    nsv4758212inversion1nstd199human GRCh37 chr4: 30,775-191,019,445 , GRCh38.p12 chr4: 30,775-190,098,290 , ADD1, 2433 more genes
    nsv4754592inversion1nstd199human GRCh37 chr4: 27,111-191,020,337 , GRCh38.p12 chr4: 27,111-190,099,182 , ADD1, 2433 more genes
    nsv4753570inversion1nstd199human GRCh37 chr4: 19,034-191,028,414 , GRCh38.p12 chr4: 19,034-190,107,259 , ADD1, 2434 more genes
    nsv4751554inversion1nstd199human GRCh37 chr4: 18,939-191,034,785 , GRCh38.p12 chr4: 18,939-190,113,630 , ADD1, 2434 more genes
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