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Items: 1 to 20 of 126

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098928copy number variation1nstd102humanUncertain significance GRCh38 chr12: 75,027,258-75,716,971 , GRCh37.p13 chr12: 75,421,038-76,110,751 LOC105369844, LOC100130268, 12 more genes
    nsv6932586copy number variation1nstd229human GRCh38 chr12: 75,472,613-75,607,690 , GRCh37.p13 chr12: 75,866,393-76,001,470 GLIPR1, LOC105369844, 2 more genes
    nsv6931491copy number variation1nstd229human GRCh38 chr12: 75,585,471-75,619,083 , GRCh37.p13 chr12: 75,979,251-76,012,863 PGDP2, LOC105369844
    nsv6930866copy number variation1nstd229human GRCh38 chr12: 75,216,232-75,678,264 , GRCh37.p13 chr12: 75,610,012-76,072,044 GLIPR1L1, KRR1, 10 more genes
    nsv6929467copy number variation1nstd229human GRCh38 chr12: 75,593,265-75,655,695 , GRCh37.p13 chr12: 75,987,045-76,049,475 LOC107984533, PGDP2, 1 more genes
    nsv6927372copy number variation1nstd229human GRCh38 chr12: 75,591,171-75,627,898 , GRCh37.p13 chr12: 75,984,951-76,021,678 PGDP2, LOC105369844
    nsv6925323copy number variation1nstd229human GRCh38 chr12: 75,592,101-75,638,000 , GRCh37.p13 chr12: 75,985,881-76,031,780 LOC105369844, PGDP2
    nsv6924104copy number variation1nstd229human GRCh38 chr12: 75,534,336-75,601,683 , GRCh37.p13 chr12: 75,928,116-75,995,463 PGDP2, LOC105369844
    nsv6637737copy number variation1nstd102humanUncertain significance GRCh37 chr12: 75,417,920-76,110,508 , GRCh38.p12 chr12: 75,024,140-75,716,728 CAPS2, GLIPR1, 13 more genes
    nsv6621840copy number variation1nstd224human GRCh37 chr12: 75,419,718-76,109,814 , GRCh38.p12 chr12: 75,025,938-75,716,034 GLIPR1, GLIPR1L1, 13 more genes
    nsv6587098inversion1nstd223human GRCh38 chr12: 70,939,082-79,478,721 , GRCh37.p13 chr12: 71,332,862-79,872,501 , H3P35, 83 more genes
    nsv6582770inversion1nstd223human GRCh38 chr12: 66,057,683-75,778,623 , GRCh37.p13 chr12: 66,451,463-76,172,403 CPSF6, TBC1D15, 135 more genes
    nsv6579681inversion1nstd223human GRCh38 chr12: 66,057,593-76,009,153 , GRCh37.p13 chr12: 66,451,373-76,402,933 SNORA113, LOC100509370, 138 more genes
    nsv6458306copy number variation1nstd223human GRCh38 chr12: 75,597,501-75,598,400 , GRCh37.p13 chr12: 75,991,281-75,992,180 LOC105369844, PGDP2
    nsv6291349copy number variation2nstd102humanUncertain significance GRCh37 chr12: 75,412,811-76,110,508 , GRCh38.p12 chr12: 75,019,031-75,716,728 RPL10P13, CAPS2, 13 more genes
    nsv6291127copy number variation1nstd102humanPathogenic GRCh37 chr12: 70,084,476-77,065,764 , GRCh38.p12 chr12: 69,690,696-76,671,984 LOC100130268, RNU6-1012P, 78 more genes
    nsv6143026copy number variation1nstd206human GRCh38 chr12: 48,500,915-111,724,058 , GRCh37.p13 chr12: 48,894,698-112,161,862 , LINC00592, 1206 more genes
    nsv6132438copy number variation1nstd213human GRCh37 chr12: 75,830,000-76,340,001 , GRCh38.p12 chr12: 75,436,220-75,946,221 GLIPR1, KRR1, 5 more genes
    nsv6132437copy number variation1nstd213human GRCh37 chr12: 75,550,000-78,060,001 , GRCh38.p12 chr12: 75,156,220-77,666,221 , CSRP2, 40 more genes
    nsv5365118translocation1nstd200human GRCh38 chr12: 75,600,425-75,600,425 , GRCh38 chr12: 75,591,044-75,591,044 , GRCh37.p13 chr12: 75,984,824-75,984,824 , GRCh37.p13 chr12: 75,994,205-75,994,205 LOC105369844, PGDP2
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