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Items: 1 to 20 of 346

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137705copy number variation1nstd102humanPathogenic GRCh37 chr9: 36,419,493-40,774,118 , GRCh38.p12 chr9: 61,281,967-67,217,006 , GRCh38.p12 chr9: 36,419,496-39,445,729 ZNF658B, LOC105379814, 208 more genes
    nsv5919501copy number variation1nstd209human GRCh38 chr9: 61,557,000-65,487,786 , GRCh37.p13 chr: NaN-NaN , MTCO1P36, 98 more genes
    nsv5918216copy number variation1nstd209human GRCh38 chr9: 61,647,960-65,578,967 , GRCh37.p13 chr: NaN-NaN , SDR42E1P3, 99 more genes
    nsv5914346copy number variation1nstd209human GRCh38 chr9: 60,768,680-66,674,368 , GRCh37.p13 chr: NaN-NaN , MEP1AP3, 146 more genes
    nsv5910323copy number variation1nstd209human GRCh38 chr9: 61,604,972-65,538,433 , GRCh37.p13 chr: NaN-NaN , FAM242E, 98 more genes
    nsv5858979copy number variation2nstd209human GRCh38 chr9: 64,488,035-64,489,699 , GRCh37.p13 chr9: 69,500,453-69,502,117 GXYLT1P6
    nsv5850399copy number variation2nstd209human GRCh38 chr9: 64,486,417-64,489,699 , GRCh37.p13 chr9: 69,498,835-69,502,117 CNN2P3, GXYLT1P6
    nsv5259774copy number variation1nstd204human GRCh38.p13 chr9: 64,487,901-64,489,700 , GRCh37.p13 chr9: 69,500,319-69,502,118 GXYLT1P6
    nsv5258557copy number variation1nstd204human GRCh38.p13 chr9: 64,486,801-64,488,700 , GRCh37.p13 chr9: 69,499,219-69,501,118 CNN2P3, GXYLT1P6
    nsv5258150copy number variation1nstd204human GRCh38.p13 chr9: 64,475,401-64,516,700 , GRCh37.p13 chr9: 69,487,819-69,529,118 CNN2P3, GXYLT1P6
    nsv5257577copy number variation1nstd204human GRCh38.p13 chr9: 64,486,401-64,487,700 , GRCh37.p13 chr9: 69,498,819-69,500,118 CNN2P3, GXYLT1P6
    nsv5254110copy number variation1nstd204human GRCh38.p13 chr9: 64,475,601-64,491,600 , GRCh37.p13 chr9: 69,488,019-69,504,018 GXYLT1P6, CNN2P3
    nsv5253267copy number variation1nstd204human GRCh38.p13 chr9: 64,489,701-64,505,000 , GRCh37.p13 chr9: 69,502,119-69,517,418 GXYLT1P6
    nsv5253220copy number variation1nstd204human GRCh38.p13 chr9: 64,486,301-64,493,300 , GRCh37.p13 chr9: 69,498,719-69,505,718 CNN2P3, GXYLT1P6
    nsv5250113copy number variation1nstd204human GRCh38.p13 chr9: 64,490,301-64,505,000 , GRCh37.p13 chr9: 69,502,719-69,517,418 GXYLT1P6
    nsv5247994copy number variation1nstd204human GRCh37.p13 chr9: 69,475,419-69,573,618 , GRCh38.p13 chr9: 64,463,001-64,561,200 CNN2P3, GXYLT1P6, 4 more genes
    nsv5246626copy number variation1nstd204human GRCh38.p13 chr9: 64,486,301-64,566,700 , GRCh37.p13 chr9: 69,498,719-69,579,118 GXYLT1P6, CNN2P3
    nsv5245815copy number variation1nstd204human GRCh38.p13 chr9: 64,490,301-64,510,400 , GRCh37.p13 chr9: 69,502,719-69,522,818 GXYLT1P6
    nsv5244829copy number variation1nstd204human GRCh38.p13 chr9: 64,476,601-64,492,300 , GRCh37.p13 chr9: 69,489,019-69,504,718 GXYLT1P6, CNN2P3
    nsv5243740copy number variation1nstd204human GRCh38.p13 chr9: 64,488,215-64,489,699 , GRCh37.p13 chr9: 69,500,633-69,502,117 GXYLT1P6
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