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Items: 1 to 20 of 329

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099181copy number variation1nstd231human GRCh38.p12 chr1: 18,899,486-20,046,918 , GRCh37 chr1: 19,225,980-20,373,411 CAPZB, HTR6, 32 more genes
    nsv7098827copy number variation1nstd102humanPathogenic GRCh37 chr1: 4,481,271-20,530,242 , GRCh38.p12 chr1: 4,421,211-20,203,749 LOC107985467, LINC01777, 386 more genes
    nsv7095949copy number variation1nstd102humanUncertain significance GRCh37 chr1: 19,199,339-24,690,861 , GRCh38.p12 chr1: 18,872,845-24,364,371 RPL29P6, NBPF3, 156 more genes
    nsv7095496copy number variation3nstd102humanUncertain significance GRCh37 chr1: 19,199,339-22,987,879 , GRCh38.p12 chr1: 18,872,845-22,661,386 RN7SL277P, MPHOSPH6P1, 103 more genes
    nsv7053544inversion1nstd229human GRCh38 chr1: 19,112,180-19,119,691 , GRCh37.p13 chr1: 19,438,674-19,446,185 UBR4
    nsv7049927inversion1nstd229human GRCh38 chr1: 12,447,483-21,286,051 , GRCh37.p13 chr1: 12,507,539-21,612,544 SLC25A34, RNA5SP41, 238 more genes
    nsv6646941copy number variation1nstd229human GRCh38 chr1: 19,114,509-19,118,802 , GRCh37.p13 chr1: 19,441,003-19,445,296 UBR4
    nsv6646874copy number variation1nstd229human GRCh38 chr1: 19,200,551-19,292,975 , GRCh37.p13 chr1: 19,527,045-19,619,469 AKR7L, EMC1, 5 more genes
    nsv6646873copy number variation1nstd229human GRCh38 chr1: 19,146,694-19,147,247 , GRCh37.p13 chr1: 19,473,188-19,473,741 UBR4
    nsv6646872copy number variation1nstd229human GRCh38 chr1: 19,074,400-19,075,583 , GRCh37.p13 chr1: 19,400,894-19,402,077 UBR4
    nsv6646787copy number variation1nstd229human GRCh38 chr1: 19,151,466-19,154,531 , GRCh37.p13 chr1: 19,477,960-19,481,025 UBR4
    nsv6646786copy number variation1nstd229human GRCh38 chr1: 19,146,123-19,244,963 , GRCh37.p13 chr1: 19,472,617-19,571,457 UBR4, EMC1-AS1, 1 more genes
    nsv6646785copy number variation1nstd229human GRCh38 chr1: 19,130,012-19,135,905 , GRCh37.p13 chr1: 19,456,506-19,462,399 UBR4
    nsv6646783copy number variation1nstd229human GRCh38 chr1: 19,069,501-19,083,200 , GRCh37.p13 chr1: 19,395,995-19,409,694 UBR4
    nsv6646589copy number variation1nstd229human GRCh38 chr1: 18,782,901-19,372,400 , GRCh37.p13 chr1: 19,109,395-19,698,894 MIR4695, AKR7A3, 15 more genes
    nsv6646405copy number variation1nstd229human GRCh38 chr1: 19,145,507-19,145,530 , GRCh37.p13 chr1: 19,472,001-19,472,024 UBR4
    nsv6646404copy number variation1nstd229human GRCh38 chr1: 19,141,439-19,145,193 , GRCh37.p13 chr1: 19,467,933-19,471,687 UBR4
    nsv6326094copy number variation1nstd223human GRCh38 chr1: 19,130,012-19,135,902 , GRCh37.p13 chr1: 19,456,506-19,462,396 UBR4
    nsv6320963copy number variation1nstd223human GRCh38 chr1: 19,111,688-19,192,016 , GRCh37.p13 chr1: 19,438,182-19,518,510 UBR4
    nsv6290472copy number variation1nstd102humanPathogenic GRCh37 chr1: 16,773,001-20,221,073 , GRCh38.p12 chr1: 16,446,506-19,894,580 MIR1290, RNU6-1099P, 92 more genes
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