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Items: 1 to 20 of 107

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5920900copy number variation1nstd209human GRCh38 chr9: 107,486,884-107,486,944 , GRCh37.p13 chr9: 110,249,165-110,249,225 KLF4
    nsv5912832copy number variation1nstd209human GRCh38 chr9: 107,487,627-107,487,677 , GRCh37.p13 chr9: 110,249,908-110,249,958 KLF4
    nsv5596133copy number variation1nstd207human GRCh38 chr9: 107,486,884-107,486,944 , GRCh37.p13 chr9: 110,249,165-110,249,225 KLF4
    nsv5379469translocation1nstd200human GRCh38 chr9: 107,483,094-107,483,094 , GRCh38 chr9: 107,482,094-107,482,094 , GRCh37.p13 chr9: 110,244,375-110,244,375 , GRCh37.p13 chr9: 110,245,375-110,245,375 KLF4
    nsv5040732inversion1nstd200human GRCh38 chr9: 100,673,006-127,581,711 , GRCh37.p13 chr9: 103,435,288-130,343,990 , LOC105379839, 440 more genes
    nsv4983054copy number variation1nstd200human GRCh38 chr9: 107,489,996-107,490,093 , GRCh37.p13 chr9: 110,252,277-110,252,374 , KLF4
    nsv4983053copy number variation1nstd200human GRCh38 chr9: 107,482,093-107,484,241 , GRCh37.p13 chr9: 110,244,374-110,246,522 KLF4
    nsv4837780copy number variation1nstd200human GRCh37 chr9: 110,246,910-110,247,083 , GRCh38.p12 chr9: 107,484,629-107,484,802 KLF4
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4455186copy number variation1nstd102humanPathogenic GRCh37 chr9: 71,416,475-141,020,389 , GRCh38.p12 chr9: 68,801,559-138,125,937 LOC105376327, ENG, 1304 more genes
    nsv4337085sequence alteration1nstd166human GRCh37.p13 chr9: 91,988,635-138,279,888 , GRCh38.p12 chr9: 89,373,720-135,388,042 , ABCA1, 927 more genes
    nsv4192075copy number variation1nstd166human GRCh37.p13 chr9: 110,244,375-110,246,449 , GRCh38.p12 chr9: 107,482,094-107,484,168 KLF4
    nsv4186695copy number variation1nstd166human GRCh37.p13 chr9: 110,203,982-110,412,618 , GRCh38.p12 chr9: 107,441,701-107,650,337 , KLF4, 6 more genes
    nsv4182568copy number variation1nstd166human GRCh37.p13 chr9: 110,246,910-110,247,083 , GRCh38.p12 chr9: 107,484,629-107,484,802 KLF4
    nsv3922685copy number variation1nstd102humanPathogenic GRCh38 chr9: 88,522,292-113,687,796 , NCBI36 chr9: 90,327,027-115,489,897 , GRCh37 chr9: 91,137,207-116,450,076 MUSK, LOC105376176, 464 more genes
    nsv3922684copy number variation2nstd102humanPathogenic NCBI36 chr9: 194,193-140,193,718 , GRCh38 chr9: 193,412-138,179,445 , GRCh37 chr9: 204,193-141,073,897 TDRD7, CDK9, 2170 more genes
    nsv3922633copy number variation2nstd102humanPathogenic GRCh38 chr9: 99,138,048-115,011,033 , NCBI36 chr9: 100,940,151-116,813,133 , GRCh37 chr9: 101,900,330-117,773,312 RAD23B, RNU6-432P, 262 more genes
    nsv3922551copy number variation1nstd102humanPathogenic GRCh38 chr9: 95,061,030-108,695,569 , NCBI36 chr9: 96,863,133-110,497,670 , GRCh37 chr9: 97,823,312-111,457,849 HEMGN, LOC105376183, 243 more genes
    nsv3921598copy number variation1nstd102humanPathogenic GRCh38 chr9: 203,861-138,125,937 , NCBI36 chr9: 193,861-140,140,210 , GRCh37 chr9: 203,861-141,020,389 PGAP4, ECPAS, 2167 more genes
    nsv3920713copy number variation1nstd102humanPathogenic NCBI36 chr9: 193,862-140,140,210 , GRCh38 chr9: 203,862-138,125,937 , GRCh37 chr9: 203,862-141,020,389 ABHD17B, LOC100533707, 2167 more genes
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