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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093619copy number variation1nstd228human GRCh37 chr4: 171,508,974-190,957,473 , GRCh38.p12 chr4: 170,587,823-190,036,318 AGA, SLC25A4, 240 more genes
    nsv7056086inversion1nstd229human GRCh38 chr4: 174,912,619-184,252,538 , GRCh37.p13 chr4: 175,833,770-185,173,691 WDR17, LOC105377580, 84 more genes
    nsv6750923copy number variation1nstd229human GRCh38 chr4: 176,272,550-176,752,778 , GRCh37.p13 chr4: 177,193,701-177,673,932 ASB5, LOC100421630, 3 more genes
    nsv6634364copy number variation1nstd102humanPathogenic GRCh37 chr4: 167,779,888-190,957,473 , GRCh38.p12 chr4: 166,858,737-190,036,318 LOC101928551, LOC107986330, 279 more genes
    nsv6634351copy number variation1nstd102humanPathogenic GRCh37 chr4: 159,174,483-190,957,473 , GRCh38.p12 chr4: 158,253,331-190,036,318 COPS3P1, LOC339975, 363 more genes
    nsv6570050inversion1nstd223human GRCh38 chr4: 169,780,525-178,315,900 , GRCh37.p13 chr4: 170,701,676-179,237,054 LOC101928409, LOC100131553, 91 more genes
    nsv6393022copy number variation1nstd223human GRCh38 chr4: 176,318,201-176,320,900 , GRCh37.p13 chr4: 177,239,352-177,242,051 SPCS3
    nsv6392196copy number variation1nstd223human GRCh38 chr4: 176,325,180-176,331,713 , GRCh37.p13 chr4: 177,246,331-177,252,864 SPCS3
    nsv6378783copy number variation1nstd223human GRCh38 chr4: 176,319,301-176,321,600 , GRCh37.p13 chr4: 177,240,452-177,242,751 SPCS3
    nsv6315348copy number variation1nstd102humanPathogenic GRCh37 chr4: 174,944,132-190,957,473 , GRCh38.p12 chr4: 174,022,981-190,036,318 SPATA4, ADAM20P2, 203 more genes
    nsv6313729copy number variation1nstd102humanPathogenic GRCh37 chr4: 159,755,174-190,225,765 , GRCh38.p12 chr4: 158,834,022-189,304,611 NAF1, LOC107986200, 336 more genes
    nsv6313663copy number variation1nstd102humanPathogenic GRCh37 chr4: 175,855,408-190,957,473 , GRCh38.p12 chr4: 174,934,257-190,036,318 LINC01596, NDUFB5P1, 190 more genes
    nsv6291006copy number variation1nstd102humanUncertain significance GRCh37 chr4: 177,188,481-177,619,344 , GRCh38.p12 chr4: 176,267,330-176,698,190 HAFML, SPCS3, 3 more genes
    nsv6135072copy number variation1nstd213human GRCh37 chr4: 176,260,000-177,270,001 , GRCh38.p12 chr4: 175,338,849-176,348,850 GPM6A, SPCS3, 8 more genes
    nsv6134911copy number variation1nstd213human GRCh37 chr4: 147,270,000-190,610,001 , GRCh38.p12 chr4: 146,348,848-189,688,847 , AGA, 517 more genes
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5462109copy number variation1nstd206human GRCh38 chr4: 175,785,135-176,386,595 , GRCh37.p13 chr4: 176,706,286-177,307,746 GPM6A, SPCS3, 6 more genes
    nsv5458987copy number variation1nstd206human GRCh38 chr4: 176,330,406-176,330,472 , GRCh37.p13 chr4: 177,251,557-177,251,623 SPCS3
    nsv4944070copy number variation1nstd200human GRCh38 chr4: 176,105,965-176,401,146 , GRCh37.p13 chr4: 177,027,116-177,322,297 SPCS3, SPATA4, 2 more genes
    nsv4930124copy number variation1nstd200human GRCh38 chr4: 176,235,214-177,166,440 , GRCh37.p13 chr4: 177,156,365-178,087,594 VEGFC, SPCS3, 4 more genes
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