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Items: 1 to 20 of 124

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5902184copy number variation1nstd209human GRCh38 chr5: 170,802,809-170,802,864 , GRCh37.p13 chr5: 170,229,813-170,229,868 GABRP
    nsv5627807insertion1nstd207human GRCh38 chr5: 170,802,699-170,802,699 , GRCh37.p13 chr5: 170,229,703-170,229,703 GABRP
    nsv5565735copy number variation1nstd207human GRCh38 chr5: 170,802,699-170,802,752 , GRCh37.p13 chr5: 170,229,703-170,229,756 GABRP
    nsv4742160copy number variation1nstd199human GRCh37 chr5: 170,229,726-170,229,779 , GRCh38.p12 chr5: 170,802,722-170,802,775 GABRP
    nsv4597888copy number variation1nstd183human GRCh37 chr5: 170,063,238-170,780,570 , GRCh38.p12 chr5: 170,636,234-171,353,566 LOC107986474, GABRP, 10 more genes
    nsv4592792copy number variation1nstd183human GRCh37 chr5: 170,063,076-170,777,960 , GRCh38.p12 chr5: 170,636,072-171,350,956 KCNIP1, LOC107986473, 10 more genes
    nsv4578263copy number variation1nstd102humanPathogenic GRCh37 chr5: 166,420,934-173,324,844 , GRCh38.p12 chr5: 166,993,929-173,897,841 LINC01187, TENM2-AS1, 112 more genes
    nsv4456608copy number variation1nstd102humanUncertain significance GRCh37 chr5: 169,923,301-170,592,803 , GRCh38.p12 chr5: 170,496,297-171,165,799 LOC107986474, KCNIP1-AS1, 7 more genes
    nsv4455586copy number variation1nstd102humanPathogenic GRCh37 chr5: 156,597,181-171,166,353 , GRCh38.p12 chr5: 157,170,170-171,739,349 LOC105377677, GABRA6, 164 more genes
    nsv4124844copy number variation1nstd166human GRCh37.p13 chr5: 170,209,391-170,209,959 , GRCh38.p12 chr5: 170,782,387-170,782,955 LOC107986475, GABRP
    nsv4117506copy number variation1nstd166human GRCh37.p13 chr5: 170,210,622-170,215,743 , GRCh38.p12 chr5: 170,783,618-170,788,739 GABRP
    nsv3924400copy number variation1nstd102humanPathogenic NCBI36 chr5: 156,185,101-180,629,412 , GRCh37 chr5: 156,252,523-180,696,806 , GRCh38 chr5: 156,825,512-181,269,805 CEP192P1, ARL2BPP6, 443 more genes
    nsv3921186copy number variation1nstd102humanPathogenic GRCh38 chr5: 164,386,701-181,269,805 , GRCh37 chr5: 163,813,707-180,696,806 , NCBI36 chr5: 163,746,285-180,629,412 TENM2, LOC107986479, 347 more genes
    nsv3921182copy number variation1nstd102humanPathogenic GRCh37 chr5: 149,094,155-180,699,152 , GRCh38 chr5: 149,714,592-181,272,151 , NCBI36 chr5: 149,074,348-180,631,758 RN7SKP148, TCOF1, 553 more genes
    nsv3920339copy number variation1nstd102humanPathogenic NCBI36 chr5: 164,323,950-180,629,412 , GRCh37.p13 chr5: 164,391,372-180,696,806 , GRCh38.p12 chr5: 164,964,366-181,269,805 MIR1229, LOC105377713, 343 more genes
    nsv3918887copy number variation1nstd102humanPathogenic GRCh37 chr5: 168,761,759-180,712,302 , NCBI36 chr5: 168,694,337-180,644,908 , GRCh38 chr5: 169,334,755-181,285,301 RPS8P7, LOC107986476, 311 more genes
    nsv3914475copy number variation1nstd102humanUncertain significance GRCh37 chr5: 167,860,417-170,844,183 , GRCh38 chr5: 168,433,412-171,417,179 , NCBI36 chr5: 167,792,995-170,776,788 INSYN2B, LOC107986472, 48 more genes
    nsv3912593copy number variation1nstd102humanUncertain significance NCBI36 chr5: 332,389-180,837,866 , GRCh37.p13 chr5: 279,389-180,905,260 , GRCh38.p12 chr5: 279,274-181,478,259 LOC105378993, LOC107986375, 2492 more genes
    nsv3911021copy number variation1nstd102humanLikely benign NCBI36 chr5: 169,586,204-170,388,340 , GRCh38 chr5: 170,226,622-171,028,731 , GRCh37 chr5: 169,653,626-170,455,735 RANBP17, LOC107986474, 13 more genes
    nsv3889848copy number variation1nstd102humanPathogenic GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719 MEGF10, LOC100128407, 2080 more genes
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