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Items: 1 to 20 of 120

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7044760inversion1nstd229human GRCh38 chr1: 22,155,852-26,348,296 , GRCh37.p13 chr1: 22,482,345-26,674,787 MIR4684, PDIK1L, 120 more genes
    nsv6647673copy number variation1nstd229human GRCh38 chr1: 24,137,623-24,141,568 , GRCh37.p13 chr1: 24,464,113-24,468,058 IL22RA1
    nsv6647671copy number variation1nstd229human GRCh38 chr1: 24,113,989-24,117,780 , GRCh37.p13 chr1: 24,440,479-24,444,270 IL22RA1
    nsv6647669copy number variation1nstd229human GRCh38 chr1: 24,050,344-24,296,672 , GRCh37.p13 chr1: 24,376,834-24,623,162 LOC105376864, LOC107984931, 5 more genes
    nsv6647289copy number variation1nstd229human GRCh38 chr1: 24,143,589-24,150,439 , GRCh37.p13 chr1: 24,470,079-24,476,929 IL22RA1
    nsv6647287copy number variation1nstd229human GRCh38 chr1: 24,132,219-24,133,118 , GRCh37.p13 chr1: 24,458,709-24,459,608 IL22RA1
    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
    nsv6636837copy number variation1nstd102humanUncertain significance GRCh37 chr1: 24,409,165-24,492,808 , GRCh38.p12 chr1: 24,082,675-24,166,318 LOC105376864, MYOM3-AS1, 3 more genes
    nsv6636637copy number variation1nstd102humanUncertain significance GRCh37 chr1: 24,363,507-24,875,537 , GRCh38.p12 chr1: 24,037,017-24,549,046 LOC105376864, GRHL3, 13 more genes
    nsv6636630copy number variation1nstd102humanUncertain significance GRCh37 chr1: 24,111,522-24,614,856 , GRCh38.p12 chr1: 23,785,032-24,288,366 HMGCL, PITHD1, 20 more genes
    nsv6636627copy number variation1nstd102humanUncertain significance GRCh37 chr1: 24,111,388-24,686,443 , GRCh38.p12 chr1: 23,784,898-24,359,953 MYOM3-AS1, BTBD6P1, 23 more genes
    nsv6335143copy number variation1nstd223human GRCh38 chr1: 24,113,942-24,117,779 , GRCh37.p13 chr1: 24,440,432-24,444,269 IL22RA1
    nsv6331475copy number variation1nstd223human GRCh38 chr1: 24,132,101-24,133,700 , GRCh37.p13 chr1: 24,458,591-24,460,190 IL22RA1
    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
    nsv6133648copy number variation1nstd213human GRCh37 chr1: 23,300,000-28,930,001 , GRCh38.p12 chr1: 22,973,507-28,603,489 RUNX3, CD52, 195 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
    nsv5869202copy number variation1nstd209human GRCh38 chr1: 24,117,193-24,118,704 , GRCh37.p13 chr1: 24,443,683-24,445,194 IL22RA1
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