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Items: 1 to 20 of 160

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7005713copy number variation1nstd229human GRCh38 chr19: 33,458,650-39,721,746 , GRCh37.p13 chr19: 33,949,556-40,212,386 , TYROBP, 259 more genes
    nsv7005456copy number variation1nstd229human GRCh38 chr19: 35,863,391-36,727,332 , GRCh37.p13 chr19: 36,354,293-37,218,234 ZNF146, CLIP3, 39 more genes
    nsv6524430copy number variation1nstd223human GRCh38 chr19: 36,312,701-36,316,400 , GRCh37.p13 chr19: 36,803,603-36,807,302 LINC00665, LOC100134317
    nsv6290300copy number variation1nstd102humanPathogenic GRCh37 chr19: 19,546,923-41,313,229 , GRCh38.p12 chr19: 19,436,114-40,807,324 ZNF420, LOC105372330, 574 more genes
    nsv6133523copy number variation1nstd213human GRCh37 chr19: 34,000,000-42,200,001 , GRCh38.p12 chr19: 33,509,094-41,696,083 , ACTN4, 345 more genes
    nsv6133411copy number variation1nstd213human GRCh37 chr19: 36,670,000-36,940,001 , GRCh38.p12 chr19: 36,179,098-36,449,099 ZNF146, ZFP14, 7 more genes
    nsv6114113copy number variation1nstd186human GRCh37 chr19: 36,758,902-36,801,776 , GRCh38.p12 chr19: 36,268,000-36,310,874 LOC100134317
    nsv5668787inversion1nstd207human GRCh38 chr19: 36,159,810-36,322,017 , GRCh37.p13 chr19: 36,650,712-36,812,919 ZNF146, ZNF565, 3 more genes
    nsv5420801copy number variation1nstd206human GRCh38 chr19: 36,268,000-36,310,874 , GRCh37.p13 chr19: 36,758,902-36,801,776 LOC100134317
    nsv4680891copy number variation1nstd189human GRCh37.p13 chr19: 36,586,154-37,723,606 , GRCh38.p12 chr19: 36,095,252-37,232,704 CAPNS1, TBCB, 36 more genes
    nsv4620459copy number variation2nstd183human GRCh37 chr19: 36,751,414-36,806,636 , GRCh38.p12 chr19: 36,260,512-36,315,734 LINC00665, LOC100134317
    nsv4457372copy number variation1nstd102humanPathogenic GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575 ZNF461, LOC101927572, 735 more genes
    nsv4436633complex substitution1nstd102humanUncertain significance GRCh38.p12 chr19: 36,183,403-38,162,322 , GRCh37 chr19: 36,674,305-38,652,962 ZNF146, ZFP30, 60 more genes
    nsv4426671copy number variation1nstd174human GRCh37 chr19: 36,729,688-36,813,769 , GRCh38.p12 chr19: 36,238,786-36,322,867 ZNF565, LOC100134317, 2 more genes
    nsv4424017copy number variation1nstd174human GRCh37 chr19: 36,729,688-36,847,822 , GRCh38.p12 chr19: 36,238,786-36,356,920 ZNF146, ZFP14, 3 more genes
    nsv4417618copy number variation1nstd174human GRCh37 chr19: 36,757,242-36,807,287 , GRCh38.p12 chr19: 36,266,340-36,316,385 LINC00665, LOC100134317
    nsv4349605copy number variation1nstd102humanPathogenic GRCh37 chr19: 35,111,811-37,744,992 , GRCh38.p12 chr19: 34,620,906-37,254,090 ATP4A, RNY5P10, 129 more genes
    nsv4255425copy number variation1nstd166human GRCh37.p13 chr19: 36,802,000-36,841,000 , GRCh38.p12 chr19: 36,311,098-36,350,098 ZFP14, LINC00665, 1 more genes
    nsv3964718insertion1nstd168human GRCh38 chr19: 36,299,219-36,401,385 , GRCh37.p13 chr19: 36,790,121-36,892,287 ZFP14, ZFP82, 2 more genes
    nsv3961084inversion1nstd168human GRCh38 chr19: 36,102,738-37,299,603 , GRCh37.p13 chr19: 36,593,640-37,790,505 CAPNS1, TBCB, 38 more genes
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