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Items: 1 to 20 of 227

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057108inversion1nstd229human GRCh38 chr4: 154,728,774-156,655,899 , GRCh37.p13 chr4: 155,649,926-157,577,051 RNU2-66P, LOC105377501, 38 more genes
    nsv7048230inversion1nstd229human GRCh38 chr4: 149,781,104-157,324,460 , GRCh37.p13 chr4: 150,702,256-158,245,612 LOC107986197, LINC02273, 119 more genes
    nsv7048094inversion1nstd229human GRCh38 chr4: 155,844,059-155,966,169 , GRCh37.p13 chr4: 156,765,211-156,887,321 CTSO, LOC105377507, 2 more genes
    nsv7043564inversion1nstd229human GRCh38 chr4: 155,820,622-155,993,550 , GRCh37.p13 chr4: 156,741,774-156,914,702 CTSO, TDO2, 2 more genes
    nsv7040065inversion1nstd229human GRCh38 chr4: 155,949,752-156,115,949 , GRCh37.p13 chr4: 156,870,904-157,037,101 LOC102724785, CTSO, 1 more genes
    nsv6741670copy number variation1nstd229human GRCh38 chr4: 155,934,101-155,970,500 , GRCh37.p13 chr4: 156,855,253-156,891,652 CTSO
    nsv6738998copy number variation1nstd229human GRCh38 chr4: 155,733,737-156,363,984 , GRCh37.p13 chr4: 156,654,889-157,285,136 GUCY1A1, FTH1P21, 8 more genes
    nsv6738516copy number variation1nstd229human GRCh38 chr4: 155,583,112-156,035,647 , GRCh37.p13 chr4: 156,504,264-156,956,799 FTH1P21, TDO2, 6 more genes
    nsv6636780copy number variation1nstd102humanUncertain significance GRCh37 chr4: 156,496,867-156,951,937 , GRCh38.p12 chr4: 155,575,715-156,030,785 GUCY1B1, ASIC5, 6 more genes
    nsv6629563copy number variation1nstd224human GRCh37 chr4: 156,693,777-156,950,378 , GRCh38.p12 chr4: 155,772,625-156,029,226 , GRCh38.p12 chr4|NW_003315914.1: 1-164,536 CTSO, FTH1P21, 4 more genes
    nsv6565650inversion1nstd223human GRCh38 chr4: 155,944,516-155,967,464 , GRCh37.p13 chr4: 156,865,668-156,888,616 CTSO
    nsv6134911copy number variation1nstd213human GRCh37 chr4: 147,270,000-190,610,001 , GRCh38.p12 chr4: 146,348,848-189,688,847 , AGA, 517 more genes
    nsv6134895copy number variation1nstd213human GRCh37 chr4: 156,720,000-156,880,001 , GRCh38.p12 chr4: 155,798,848-155,958,849 , GRCh38.p12 chr4|NW_003315914.1: 1-136,121 CTSO, GUCY1B1, 3 more genes
    nsv6134884copy number variation1nstd213human GRCh37 chr4: 109,230,000-161,720,001 , GRCh38.p12 chr4: 108,308,844-160,798,849 , ANK2, 616 more genes
    nsv6134731copy number variation1nstd213human GRCh37 chr4: 109,230,000-161,710,001 , GRCh38.p12 chr4: 108,308,844-160,788,849 , ANK2, 616 more genes
    nsv6112754copy number variation1nstd102humanPathogenic GRCh37 chr4: 131,303,317-168,722,402 , GRCh38.p12 chr4: 130,382,162-167,801,251 MIR3139, CLGN, 407 more genes
    nsv5680420mobile element insertion2nstd211human GRCh38 chr4: 155,940,261-155,940,261 , GRCh37.p13 chr4: 156,861,413-156,861,413 CTSO
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5400832mobile element insertion1nstd206human GRCh38 chr4: 155,940,261-155,940,312 , GRCh37.p13 chr4: 156,861,413-156,861,464 CTSO
    nsv5377722translocation1nstd200human GRCh38 chr4: 155,967,464-155,967,464 , GRCh38 chr4: 155,944,516-155,944,516 , GRCh37.p13 chr4: 156,865,668-156,865,668 , GRCh37.p13 chr4: 156,888,616-156,888,616 CTSO
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