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Items: 1 to 20 of 131

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077519inversion1nstd229human GRCh38 chr12: 86,495,718-92,133,299 , GRCh37.p13 chr12: 86,889,495-92,527,075 CEP290, MIR3059, 60 more genes
    nsv7074415inversion1nstd229human GRCh38 chr12: 87,777,005-87,863,168 , GRCh37.p13 chr12: 88,170,782-88,256,945 MKRN9P, LINC02258, 1 more genes
    nsv7060010inversion1nstd229human GRCh38 chr12: 86,085,575-91,207,469 , GRCh37.p13 chr12: 86,479,353-91,601,246 POC1B, C12orf50, 55 more genes
    nsv6937877copy number variation1nstd229human GRCh38 chr12: 87,781,993-87,782,668 , GRCh37.p13 chr12: 88,175,770-88,176,445 LINC02258, MKRN9P
    nsv6937266copy number variation1nstd229human GRCh38 chr12: 87,669,425-87,863,293 , GRCh37.p13 chr12: 88,063,202-88,257,070 MKRN9P, CYCSP30, 3 more genes
    nsv6920810copy number variation1nstd229human GRCh38 chr12: 86,380,249-87,989,805 , GRCh37.p13 chr12: 86,774,027-88,383,582 LOC107984478, RPL23AP68, 12 more genes
    nsv6594773inversion1nstd223human GRCh38 chr12: 87,777,001-87,863,170 , GRCh37.p13 chr12: 88,170,778-88,256,947 GADD45AP1, MKRN9P, 1 more genes
    nsv6470919copy number variation1nstd223human GRCh38 chr12: 87,669,425-87,863,288 , GRCh37.p13 chr12: 88,063,202-88,257,065 LINC02258, MKRN9P, 3 more genes
    nsv6462044copy number variation1nstd223human GRCh38 chr12: 87,781,968-87,782,457 , GRCh37.p13 chr12: 88,175,745-88,176,234 LINC02258, MKRN9P
    nsv6314045copy number variation1nstd102humanUncertain significance GRCh37 chr12: 87,592,859-88,575,639 , GRCh38.p12 chr12: 87,199,082-88,181,862 LOC100420011, LOC107984542, 14 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
    nsv6132719copy number variation1nstd213human GRCh37 chr12: 87,560,000-88,490,001 , GRCh38.p12 chr12: 87,166,223-88,096,224 CYCSP30, LOC105369880, 15 more genes
    nsv6132715copy number variation1nstd213human GRCh37 chr12: 84,440,000-93,800,001 , GRCh38.p12 chr12: 84,046,221-93,406,225 , BTG1, 102 more genes
    nsv5939070copy number variation1nstd209human GRCh38 chr12: 87,781,772-87,782,259 , GRCh37.p13 chr12: 88,175,549-88,176,036 LINC02258, MKRN9P
    nsv5933951copy number variation1nstd209human GRCh38 chr12: 87,781,968-87,782,456 , GRCh37.p13 chr12: 88,175,745-88,176,233 LINC02258, MKRN9P
    nsv5696000mobile element insertion1nstd211human GRCh38 chr12: 87,782,886-87,782,886 , GRCh37.p13 chr12: 88,176,663-88,176,663 LINC02258, MKRN9P
    nsv5590134copy number variation1nstd207human GRCh38 chr12: 87,781,968-87,782,456 , GRCh37.p13 chr12: 88,175,745-88,176,233 MKRN9P, LINC02258
    nsv5498454copy number variation1nstd206human GRCh38 chr12: 87,781,662-87,782,426 , GRCh37.p13 chr12: 88,175,439-88,176,203 LINC02258, MKRN9P
    nsv5316555copy number variation1nstd204human GRCh37.p13 chr12: 88,175,746-88,176,228 , GRCh38.p13 chr12: 87,781,969-87,782,451 MKRN9P, LINC02258
    nsv5041434inversion1nstd200human GRCh38 chr12: 87,777,003-87,863,169 , GRCh37.p13 chr12: 88,170,780-88,256,946 GADD45AP1, MKRN9P, 1 more genes
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