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Items: 1 to 20 of 288

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112732copy number variation1nstd102humanPathogenic GRCh37 chr5: 13,200-4,012,072 , GRCh38.p12 chr5: 13,200-4,011,958 SLC9A3-AS1, LOC107984098, 76 more genes
    nsv5381771copy number variation1nstd102humanPathogenic GRCh37 chr5: 22,149-29,048,823 , GRCh38.p12 chr5: 22,149-29,048,716 OTULINL, AKTIPP2, 317 more genes
    nsv4944310copy number variation1nstd200human GRCh38 chr5: 3,579,000-3,637,071 , GRCh37.p13 chr5: 3,579,114-3,637,185 IRX1, LOC107986399
    nsv4936861copy number variation1nstd200human GRCh38 chr5: 3,596,775-3,596,896 , GRCh37.p13 chr5: 3,596,889-3,597,010 IRX1
    nsv4728897copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,576-4,305,172 , GRCh38.p12 chr5: 113,461-4,305,059 PPP4R2P1, MIR6075, 75 more genes
    nsv4685752copy number variation1nstd102humanPathogenic GRCh37 chr5: 71,904-22,078,969 , GRCh38.p12 chr5: 71,789-22,078,860 LINC01377, LOC100421308, 277 more genes
    nsv4674705copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,576-5,657,333 , GRCh38.p12 chr5: 113,461-5,657,220 LOC101929898, MIR4635, 90 more genes
    nsv4674549copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,576-4,325,585 , GRCh38.p12 chr5: 113,461-4,325,472 LINC01017, LOC105374614, 75 more genes
    nsv4674497copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,576-14,738,180 , GRCh38.p12 chr5: 113,461-14,738,071 LOC101929003, MTCYBP37, 192 more genes
    nsv4674444copy number variation1nstd102humanPathogenic GRCh37 chr5: 1,322,680-10,762,544 , GRCh38.p12 chr5: 1,322,565-10,762,432 LOC100132773, LINC01019, 125 more genes
    nsv4674161copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,576-23,364,376 , GRCh38.p12 chr5: 113,461-23,364,267 LOC102723561, LOC107986397, 287 more genes
    nsv4674139copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,576-5,194,484 , GRCh38.p12 chr5: 113,461-5,194,371 BRD9, LOC100310782, 84 more genes
    nsv4674130copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,576-11,767,720 , GRCh38.p12 chr5: 113,461-11,767,608 SLC9A3-AS1, LINC02114, 169 more genes
    nsv4673948copy number variation1nstd102humanUncertain significance GRCh37 chr5: 2,402,960-5,395,826 , GRCh38.p12 chr5: 2,402,846-5,395,713 LSINCT5, LOC107984098, 29 more genes
    nsv4598085copy number variation2nstd183human GRCh37 chr5: 3,594,547-3,596,541 , GRCh38.p12 chr5: 3,594,433-3,596,427 IRX1
    nsv4598083copy number variation1nstd183human GRCh37 chr5: 3,570,157-3,678,789 , GRCh38.p12 chr5: 3,570,043-3,678,675 LOC107986399, IRX1
    nsv4411688copy number variation1nstd174human GRCh37 chr5: 3,590,051-3,608,624 , GRCh38.p12 chr5: 3,589,937-3,608,510 IRX1
    nsv4400449copy number variation1nstd174human GRCh37 chr5: 3,594,547-3,597,830 , GRCh38.p12 chr5: 3,594,433-3,597,716 IRX1
    nsv4369315copy number variation1nstd173human GRCh37 chr5: 113,577-10,304,966 , GRCh38.p12 chr5: 113,462-10,304,854 , LOC105374625, 158 more genes
    nsv4349271copy number variation1nstd102humanPathogenic GRCh37 chr5: 140,474-26,906,925 , GRCh38.p12 chr5: 140,359-26,906,816 MIR4636, LRRC14B, 304 more genes
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