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Items: 1 to 20 of 93

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142915copy number variation1nstd232human GRCh37.p13 chr1: 23,885,510-23,885,616 , GRCh38.p12 chr1: 23,559,019-23,559,125 , GRCh38.p12 chr1|NW_014040926.1: 328,998-329,104 ID3
    nsv7099186copy number variation1nstd231human GRCh38.p12 chr1: 23,507,765-23,861,716 , GRCh37 chr1: 23,834,257-24,188,206 E2F2, FUCA1, 15 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
    nsv7044760inversion1nstd229human GRCh38 chr1: 22,155,852-26,348,296 , GRCh37.p13 chr1: 22,482,345-26,674,787 MIR4684, PDIK1L, 120 more genes
    nsv6647420copy number variation1nstd229human GRCh38 chr1: 23,559,728-23,569,009 , GRCh37.p13 chr1: 23,886,219-23,895,499 ID3
    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
    nsv6636481copy number variation1nstd102humanUncertain significance GRCh37 chr1: 23,680,995-24,224,241 , GRCh38.p12 chr1: 23,354,502-23,897,751 CNR2, E2F2, 20 more genes
    nsv6315455copy number variation1nstd102humanPathogenic GRCh37 chr1: 23,814,543-24,163,928 , GRCh38.p12 chr1: 23,488,050-23,837,438 LOC105376860, LOC101928163, 14 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
    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
    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
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4761183inversion1nstd199human GRCh37 chr1: 16,884,570-145,374,569 , GRCh38.p12 chr1: 16,558,075-149,528,945 , ABCA4, 2341 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4594379copy number variation1nstd183human GRCh37 chr1: 23,884,553-23,885,540 , GRCh38.p12 chr1: 23,558,062-23,559,049 , GRCh38.p12 chr1|NW_014040926.1: 328,041-329,028 ID3
    nsv4580809copy number variation1nstd183human GRCh37 chr1: 23,884,427-23,886,586 , GRCh38.p12 chr1|NW_014040926.1: 327,915-330,074 , GRCh38.p12 chr1: 23,557,936-23,560,095 ID3
    nsv4580547copy number variation1nstd183human GRCh37 chr1: 23,885,376-23,885,535 , GRCh38.p12 chr1: 23,558,885-23,559,044 , GRCh38.p12 chr1|NW_014040926.1: 328,864-329,023 ID3
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