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Items: 1 to 20 of 159

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5494029copy number variation1nstd206human GRCh38 chr12: 110,699,970-110,715,913 , GRCh37.p13 chr12: 111,137,775-111,153,718 PPP1CC, HVCN1
    nsv5319183copy number variation1nstd204human GRCh38.p13 chr12: 110,699,943-110,715,938 , GRCh37.p13 chr12: 111,137,748-111,153,743 PPP1CC, HVCN1
    nsv5317310copy number variation1nstd204human GRCh38.p13 chr12: 110,697,077-110,702,295 , GRCh37.p13 chr12: 111,134,882-111,140,100 HVCN1
    nsv5276631copy number variation1nstd204human GRCh38.p13 chr12: 110,699,934-110,709,741 , GRCh37.p13 chr12: 111,137,739-111,147,546 PPP1CC, HVCN1
    nsv5274613copy number variation1nstd204human GRCh38.p13 chr12: 110,696,597-110,702,571 , GRCh37.p13 chr12: 111,134,402-111,140,376 HVCN1
    nsv5263598copy number variation1nstd204human GRCh38.p13 chr12: 110,661,557-110,663,756 , GRCh37.p13 chr12: 111,099,362-111,101,561 HVCN1
    nsv4995591copy number variation1nstd200human GRCh38 chr12: 110,672,461-110,672,586 , GRCh37.p13 chr12: 111,110,266-111,110,391 HVCN1
    nsv4830267copy number variation1nstd200human GRCh37 chr12: 111,110,266-111,110,391 , GRCh38.p12 chr12: 110,672,461-110,672,586 HVCN1
    nsv4756208inversion1nstd199human GRCh37 chr12: 104,359,633-125,801,147 , GRCh38.p12 chr12: 103,965,855-125,316,601 , ACACB, 453 more genes
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
    nsv4754840inversion1nstd199human GRCh37 chr12: 104,382,539-125,801,164 , GRCh38.p12 chr12: 103,988,761-125,316,618 , ACACB, 452 more genes
    nsv4736781copy number variation1nstd199human GRCh37 chr12: 25,957,322-125,801,148 , GRCh38.p12 chr12: 25,804,388-125,316,602 , RNA5SP368, 1787 more genes
    nsv4728881copy number variation1nstd102humanPathogenic GRCh37 chr12: 106,498,814-112,252,906 , GRCh38.p12 chr12: 106,105,036-111,815,102 ATP2A2, CUX2, 115 more genes
    nsv4672099copy number variation1nstd186human GRCh37 chr12: 111,137,848-111,146,971 , GRCh38.p12 chr12: 110,700,043-110,709,166 PPP1CC, HVCN1
    nsv4615311copy number variation2nstd183human GRCh37 chr12: 111,137,848-111,146,971 , GRCh38.p12 chr12: 110,700,043-110,709,166 PPP1CC, HVCN1
    nsv4602908copy number variation1nstd183human GRCh37 chr12: 111,131,806-111,149,788 , GRCh38.p12 chr12: 110,694,001-110,711,983 HVCN1, PPP1CC
    nsv4421570copy number variation1nstd174human GRCh37 chr12: 111,136,224-111,146,971 , GRCh38.p12 chr12: 110,698,419-110,709,166 PPP1CC, HVCN1
    nsv4223262copy number variation1nstd166human GRCh37.p13 chr12: 111,123,591-111,123,746 , GRCh38.p12 chr12: 110,685,786-110,685,941 HVCN1
    nsv4217164copy number variation1nstd166human GRCh37.p13 chr12: 111,137,712-111,153,718 , GRCh38.p12 chr12: 110,699,907-110,715,913 PPP1CC, HVCN1
    nsv3956075insertion1nstd168human GRCh38 chr12: 110,701,211-110,719,376 , GRCh37.p13 chr12: 111,139,016-111,157,181 PPP1CC, HVCN1
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