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Items: 1 to 20 of 297

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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
    nsv7054725inversion1nstd229human GRCh38 chr4: 178,850,585-188,333,056 , GRCh37.p13 chr4: 179,771,739-189,254,210 RPL6P16, LOC105377568, 125 more genes
    nsv7054658inversion1nstd229human GRCh38 chr4: 183,954,061-185,864,650 , GRCh37.p13 chr4: 184,875,214-186,785,804 IRF2, LOC105377590, 39 more genes
    nsv7053039inversion1nstd229human GRCh38 chr4: 183,766,927-184,811,271 , GRCh37.p13 chr4: 184,688,080-185,732,425 LOC105377582, ENPP6, 18 more genes
    nsv7051710inversion1nstd229human GRCh38 chr4: 184,496,747-186,979,683 , GRCh37.p13 chr4: 185,417,901-187,900,837 LOC102723906, LINC02436, 47 more genes
    nsv7048281inversion1nstd229human GRCh38 chr4: 177,590,230-186,282,308 , GRCh37.p13 chr4: 178,511,384-187,203,462 STOX2, LINC01098, 105 more genes
    nsv6756944copy number variation1nstd229human GRCh38 chr4: 184,402,149-185,513,891 , GRCh37.p13 chr4: 185,323,303-186,435,045 LINC02365, SNX25, 27 more genes
    nsv6753568copy number variation1nstd229human GRCh38 chr4: 184,646,859-184,646,915 , GRCh37.p13 chr4: 185,568,013-185,568,069 CASP3
    nsv6753305copy number variation1nstd229human GRCh38 chr4: 184,553,201-184,755,400 , GRCh37.p13 chr4: 185,474,355-185,676,554 ACSL1, PRIMPOL, 4 more genes
    nsv6747995copy number variation1nstd229human GRCh38 chr4: 184,624,101-184,627,400 , GRCh37.p13 chr4: 185,545,255-185,548,554 CASP3, LINC02365
    nsv6745886copy number variation1nstd229human GRCh38 chr4: 184,539,137-184,649,010 , GRCh37.p13 chr4: 185,460,291-185,570,164 PRIMPOL, LOC100129245, 2 more genes
    nsv6745121copy number variation1nstd229human GRCh38 chr4: 184,532,501-184,694,600 , GRCh37.p13 chr4: 185,453,655-185,615,754 LINC02365, PRIMPOL, 4 more genes
    nsv6744840copy number variation1nstd229human GRCh38 chr4: 184,538,853-188,245,346 , GRCh37.p13 chr4: 185,460,007-189,166,500 F11-AS1, SORBS2, 66 more genes
    nsv6740569copy number variation1nstd229human GRCh38 chr4: 184,589,401-184,694,500 , GRCh37.p13 chr4: 185,510,555-185,615,654 CENPU, CASP3, 2 more genes
    nsv6740471copy number variation1nstd229human GRCh38 chr4: 184,587,311-184,638,673 , GRCh37.p13 chr4: 185,508,465-185,559,827 CASP3, LINC02365
    nsv6636301copy number variation1nstd102humanPathogenic GRCh37 chr4: 183,694,501-190,957,473 , GRCh38.p12 chr4: 182,773,348-190,036,318 LOC105377588, ENPP6, 139 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
    nsv6634350copy number variation1nstd102humanPathogenic GRCh37 chr4: 185,211,271-190,957,473 , GRCh38.p12 chr4: 184,290,118-190,036,318 LINC02374, SLED1, 102 more genes
    nsv6629399copy number variation1nstd224human GRCh37 chr4: 185,543,672-186,029,032 , GRCh38.p12 chr4: 184,622,518-185,107,878 PRIMPOL, HELT, 13 more genes
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