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Items: 1 to 20 of 286

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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
    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
    nsv7045590inversion1nstd229human GRCh38 chr4: 184,865,780-184,988,144 , GRCh37.p13 chr4: 185,786,934-185,909,298 LINC01093, MIR4455, 1 more genes
    nsv7045478inversion1nstd229human GRCh38 chr4: 184,811,410-187,241,218 , GRCh37.p13 chr4: 185,732,564-188,162,372 RPSAP70, MIR3945, 42 more genes
    nsv7041443inversion1nstd229human GRCh38 chr4: 184,880,457-184,962,145 , GRCh37.p13 chr4: 185,801,611-185,883,299 LINC01093, MIR4455
    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
    nsv6756931copy number variation1nstd229human GRCh38 chr4: 184,811,611-184,933,734 , GRCh37.p13 chr4: 185,732,765-185,854,888 LINC01093, LOC105377587, 3 more genes
    nsv6753828copy number variation1nstd229human GRCh38 chr4: 184,892,331-184,892,994 , GRCh37.p13 chr4: 185,813,485-185,814,148 LINC01093
    nsv6752452copy number variation1nstd229human GRCh38 chr4: 184,890,166-184,901,429 , GRCh37.p13 chr4: 185,811,320-185,822,583 LINC01093
    nsv6745541copy number variation1nstd229human GRCh38 chr4: 184,890,706-184,891,037 , GRCh37.p13 chr4: 185,811,860-185,812,191 LINC01093
    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
    nsv6743928copy number variation1nstd229human GRCh38 chr4: 184,870,901-185,007,000 , GRCh37.p13 chr4: 185,792,055-185,928,154 LINC01093, LINC02437, 1 more genes
    nsv6743656copy number variation1nstd229human GRCh38 chr4: 184,858,701-185,004,800 , GRCh37.p13 chr4: 185,779,855-185,925,954 LINC01093, LINC02437, 1 more genes
    nsv6742418copy number variation1nstd229human GRCh38 chr4: 184,889,049-184,891,874 , GRCh37.p13 chr4: 185,810,203-185,813,028 LINC01093
    nsv6636309copy number variation1nstd102humanPathogenic GRCh37 chr4: 185,748,860-188,413,920 , GRCh38.p12 chr4: 184,827,706-187,492,766 ANKRD37, RNU6-1055P, 45 more genes
    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
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