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Items: 1 to 20 of 144

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099184copy number variation1nstd231human GRCh38.p12 chr1: 21,486,574-23,087,716 , GRCh37 chr1: 21,813,067-23,414,209 ALPL, C1QA, 36 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
    nsv7044083inversion1nstd229human GRCh38 chr1: 22,142,029-22,142,209 , GRCh37.p13 chr1: 22,468,522-22,468,702 WNT4, LOC105376845
    nsv6647435copy number variation1nstd229human GRCh38 chr1: 22,122,621-22,126,645 , GRCh37.p13 chr1: 22,449,114-22,453,138 WNT4
    nsv6647434copy number variation1nstd229human GRCh38 chr1: 22,120,579-22,122,617 , GRCh37.p13 chr1: 22,447,072-22,449,110 WNT4
    nsv6647254copy number variation1nstd229human GRCh38 chr1: 21,562,611-27,513,090 , GRCh37.p13 chr1: 21,889,104-27,839,601 RPL18AP5, LINC00339, 184 more genes
    nsv6647227copy number variation1nstd229human GRCh38 chr1: 20,848,934-27,947,465 , GRCh37.p13 chr1: 21,175,427-28,273,976 RPL17P9, ALPL, 218 more genes
    nsv6160898copy number variation1nstd214human GRCh38 chr1: 22,119,106-22,119,250 , GRCh37.p13 chr1: 22,445,599-22,445,743 WNT4
    nsv6137724copy number variation1nstd102humanPathogenic GRCh37 chr1: 16,785,250-23,491,592 , GRCh38.p12 chr1: 16,458,755-23,165,099 PADI1, RPS15AP6, 176 more genes
    nsv6133948copy number variation1nstd213human GRCh37 chr1: 17,280,000-26,950,001 , GRCh38.p12 chr1: 16,953,505-26,623,510 ALPL, C1QA, 250 more genes
    nsv6133748copy number variation1nstd213human GRCh37 chr1: 17,270,000-26,960,001 , GRCh38.p12 chr1: 16,943,505-26,633,510 ALPL, C1QA, 250 more genes
    nsv6133629copy number variation1nstd213human GRCh37 chr1: 20,630,000-22,600,001 , GRCh38.p12 chr1: 20,303,507-22,273,508 ALPL, CDA, 52 more genes
    nsv6133572copy number variation1nstd213human GRCh37 chr1: 17,270,000-26,950,001 , GRCh38.p12 chr1: 16,943,505-26,623,510 ALPL, C1QA, 250 more genes
    nsv5982586copy number variation1nstd212human GRCh38 chr1: 22,123,055-22,125,021 , GRCh37.p13 chr1: 22,449,548-22,451,514 WNT4
    nsv5431644copy number variation1nstd206human GRCh38 chr1: 22,123,052-22,125,030 , GRCh37.p13 chr1: 22,449,545-22,451,523 WNT4
    nsv5431562copy number variation1nstd206human GRCh38 chr1: 22,119,074-22,119,193 , GRCh37.p13 chr1: 22,445,567-22,445,686 WNT4
    nsv5427686copy number variation1nstd206human GRCh38 chr1: 22,064,395-28,290,354 , GRCh37.p13 chr1: 22,390,888-28,616,865 , NCMAP-DT, 201 more genes
    nsv5280612copy number variation1nstd204human GRCh38.p13 chr1: 22,123,042-22,125,039 , GRCh37.p13 chr1: 22,449,535-22,451,532 WNT4
    nsv5208619copy number variation1nstd204human GRCh38.p13 chr1: 22,123,176-22,125,175 , GRCh37.p13 chr1: 22,449,669-22,451,668 WNT4
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