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Items: 1 to 20 of 377

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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
    nsv7045478inversion1nstd229human GRCh38 chr4: 184,811,410-187,241,218 , GRCh37.p13 chr4: 185,732,564-188,162,372 RPSAP70, MIR3945, 42 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
    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
    nsv6754930copy number variation1nstd229human GRCh38 chr4: 184,846,001-184,848,000 , GRCh37.p13 chr4: 185,767,155-185,769,154 MIR3945HG
    nsv6753704copy number variation1nstd229human GRCh38 chr4: 184,845,978-184,847,984 , GRCh37.p13 chr4: 185,767,132-185,769,138 MIR3945HG
    nsv6749277copy number variation1nstd229human GRCh38 chr4: 184,727,501-184,863,700 , GRCh37.p13 chr4: 185,648,655-185,784,854 ACSL1, SLED1, 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
    nsv6744073copy number variation1nstd229human GRCh38 chr4: 184,840,720-184,848,380 , GRCh37.p13 chr4: 185,761,874-185,769,534 MIR3945HG, LOC105377587
    nsv6743190copy number variation1nstd229human GRCh38 chr4: 184,840,701-184,849,500 , GRCh37.p13 chr4: 185,761,855-185,770,654 MIR3945HG, LOC105377587, 1 more genes
    nsv6738671copy number variation1nstd229human GRCh38 chr4: 184,826,540-184,856,523 , GRCh37.p13 chr4: 185,747,694-185,777,677 MIR3945HG, ACSL1, 2 more genes
    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
    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
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