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Items: 1 to 20 of 143

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5952034insertion1nstd209human GRCh38 chr3: 44,572,849-44,572,849 , GRCh37.p13 chr3: 44,614,341-44,614,341 ZKSCAN7-AS1, ZKSCAN7
    nsv5674433mobile element insertion1nstd211human GRCh38 chr3: 44,555,740-44,555,740 , GRCh37.p13 chr3: 44,597,232-44,597,232 ZKSCAN7-AS1, ZKSCAN7
    nsv5411515mobile element insertion1nstd206human GRCh38 chr3: 44,555,740-44,555,791 , GRCh37.p13 chr3: 44,597,232-44,597,283 ZKSCAN7-AS1, ZKSCAN7
    nsv5067209mobile element insertion1nstd203human GRCh38 chr3: 44,558,336-44,558,362 , GRCh37.p13 chr3: 44,599,828-44,599,854 ZKSCAN7, ZKSCAN7-AS1
    nsv5037434inversion1nstd200human GRCh38 chr3: 5,031,119-56,902,223 , GRCh37.p13 chr3: 5,072,804-56,936,251 , IRAK2, 925 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    nsv4911052copy number variation1nstd200human GRCh38 chr3: 44,570,612-44,570,668 , GRCh37.p13 chr3: 44,612,104-44,612,160 ZKSCAN7-AS1, ZKSCAN7
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 more genes
    nsv4877503inversion1nstd200human GRCh37 chr3: 24,885,632-100,711,157 , GRCh38.p12 chr3: 24,844,141-100,992,313 , LINC00692, 1088 more genes
    nsv4790494copy number variation1nstd200human GRCh37 chr3: 44,612,104-44,612,160 , GRCh38.p12 chr3: 44,570,612-44,570,668 , GRCh38.p12 chr3|NW_009646197.1: 95,966-96,022 ZKSCAN7-AS1, ZKSCAN7
    nsv4674744copy number variation1nstd102humanUncertain significance GRCh37 chr3: 44,444,902-45,413,927 , GRCh38.p12 chr3: 44,403,410-45,372,435 RPL12P44, TMEM42, 37 more genes
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
    nsv4470951mobile element insertion1nstd166human GRCh37.p13 chr3: 44,597,221-44,597,221 , GRCh38.p12 chr3|NW_009646197.1: 81,083-81,083 , GRCh38.p12 chr3: 44,555,729-44,555,729 ZKSCAN7-AS1, ZKSCAN7
    nsv4085809copy number variation1nstd166human GRCh37.p13 chr3: 44,602,172-44,624,525 , GRCh38.p12 chr3: 44,560,680-44,583,033 , GRCh38.p12 chr3|NW_009646197.1: 86,034-108,387 ZNF660, MPRIPP1, 3 more genes
    nsv4075978copy number variation1nstd166human GRCh37.p13 chr3: 44,621,229-44,621,397 , GRCh38.p12 chr3|NW_009646197.1: 105,091-105,259 , GRCh38.p12 chr3: 44,579,737-44,579,905 MPRIPP1, ZKSCAN7-AS1, 1 more genes
    nsv3967356copy number variation1nstd168human GRCh38 chr3: 44,583,269-44,626,657 , GRCh37.p13 chr3: 44,624,761-44,668,149 ZNF197, ZKSCAN7, 4 more genes
    nsv3889228copy number variation2nstd102humanPathogenic GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115 NDUFB4, LOC105374108, 2876 more genes
    nsv3885606copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156 RNU4-62P, SEMA3B-AS1, 2880 more genes
    nsv3885169copy number variation1nstd102humanPathogenic GRCh37 chr3: 16,923,595-45,249,923 , GRCh38.p12 chr3: 16,884,818-45,208,431 RNU6-243P, ZNF385D, 382 more genes
    nsv3883164copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 37,028,313-49,929,220 , GRCh38.p12 chr3: 36,986,822-49,891,787 ACAA1, ACVR2B, 344 more genes
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