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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7141228copy number variation1nstd232human GRCh37.p13 chr1: 206,546,250-206,546,318 , GRCh38.p12 chr1: 206,372,896-206,372,965 SRGAP2
    nsv7099257copy number variation1nstd231human GRCh38.p12 chr1: 203,396,218-207,103,915 , GRCh37 chr1: 203,365,346-207,277,260 ATP2B4, AVPR1B, 116 more genes
    nsv7095955copy number variation1nstd102humanUncertain significance GRCh37 chr1: 200,522,516-206,945,780 , GRCh38.p12 chr1: 200,553,388-206,772,435 ELF3, MAPKAPK2, 189 more genes
    nsv7095569copy number variation2nstd102humanUncertain significance GRCh37 chr1: 200,522,516-208,391,267 , GRCh38.p12 chr1: 200,553,388-208,217,922 TRK-TTT8-1, ADIPOR1, 228 more genes
    nsv7044092inversion1nstd229human GRCh38 chr1: 203,118,726-211,305,271 , GRCh37.p13 chr1: 203,087,854-211,478,613 LOC100420418, LINC00260, 201 more genes
    nsv6674148copy number variation1nstd229human GRCh38 chr1: 206,463,901-206,466,600 , GRCh37.p13 chr1|NW_003871057.1: 454,755-457,454 , GRCh37.p13 chr1: 206,637,241-206,639,939 SRGAP2
    nsv6668094copy number variation1nstd229human GRCh38 chr1: 206,459,007-206,459,112 , GRCh37.p13 chr1: 206,632,353-206,632,458 , GRCh37.p13 chr1|NW_003871057.1: 449,861-449,966 SRGAP2
    nsv6666553copy number variation1nstd229human GRCh38 chr1: 206,457,504-206,464,719 , GRCh37.p13 chr1: 206,630,850-206,638,059 , GRCh37.p13 chr1|NW_003871057.1: 448,358-455,573 SRGAP2
    nsv6636965copy number variation1nstd102humanPathogenic GRCh37 chr1: 181,453,460-213,107,248 , GRCh38.p12 chr1: 181,484,324-212,933,906 PRELP, SYT14, 527 more genes
    nsv6634372copy number variation1nstd102humanPathogenic GRCh37 chr1: 197,867,914-249,224,684 , GRCh38.p12 chr1: 197,898,784-248,930,485 LOC105373279, YBX1P9, 1036 more genes
    nsv6554773inversion1nstd223human GRCh38 chr1: 204,500,842-208,290,127 , GRCh37.p13 chr1: 204,469,970-208,463,472 RNA5SP75, LOC105372869, 108 more genes
    nsv6549026inversion1nstd223human GRCh38 chr1: 206,443,544-206,443,945 , GRCh37.p13 chr1: 206,616,894-206,617,291 , GRCh37.p13 chr1|NW_003871057.1: 434,398-434,799 SRGAP2
    nsv6536402inversion1nstd223human GRCh38 chr1: 206,452,871-206,452,947 , GRCh37.p13 chr1|NW_003871057.1: 443,725-443,801 , GRCh37.p13 chr1: 206,626,215-206,626,293 SRGAP2
    nsv6323596copy number variation1nstd223human GRCh38 chr1: 206,434,330-206,435,058 , GRCh37.p13 chr1|NW_003871057.1: 425,184-425,912 , GRCh37.p13 chr1: 206,607,680-206,608,408 SRGAP2
    nsv6318186copy number variation1nstd223human GRCh38 chr1: 206,417,138-206,417,452 , GRCh37.p13 chr1|NW_003871057.1: 407,992-408,306 , GRCh37.p13 chr1: 206,590,498-206,590,812 SRGAP2
    nsv6293967mobile element insertion1nstd186human GRCh37 chr1: 206,606,237-206,606,288 , GRCh38.p12 chr1: 206,432,887-206,432,938 SRGAP2
    nsv6293731mobile element insertion1nstd186human GRCh37 chr1: 206,615,030-206,615,081 , GRCh38.p12 chr1: 206,441,680-206,441,731 SRGAP2
    nsv6258076mobile element insertion1nstd215human GRCh38 chr1: 206,443,212-206,443,212 , GRCh37.p13 chr1|NW_003871057.1: 434,066-434,066 , GRCh37.p13 chr1: 206,616,562-206,616,562 SRGAP2
    nsv6258075mobile element insertion1nstd215human GRCh38 chr1: 206,441,680-206,441,680 , GRCh37.p13 chr1|NW_003871057.1: 432,534-432,534 , GRCh37.p13 chr1: 206,615,030-206,615,030 SRGAP2
    nsv6258074mobile element insertion1nstd215human GRCh38 chr1: 206,438,720-206,438,720 , GRCh37.p13 chr1|NW_003871057.1: 429,574-429,574 , GRCh37.p13 chr1: 206,612,070-206,612,070 SRGAP2
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