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Items: 1 to 20 of 122

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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
    nsv6647668copy number variation1nstd229human GRCh38 chr1: 23,976,715-24,015,575 , GRCh37.p13 chr1: 24,303,205-24,342,065 LOC105376863, LOC105378615, 2 more genes
    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
    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
    nsv6316387copy number variation1nstd223human GRCh38 chr1: 23,972,379-23,972,726 , GRCh37.p13 chr1: 24,298,869-24,299,216 SRSF10
    nsv6257558mobile element insertion1nstd215human GRCh38 chr1: 23,977,871-23,977,871 , GRCh37.p13 chr1: 24,304,361-24,304,361 SRSF10
    nsv6133987copy number variation1nstd213human GRCh37 chr1: 24,010,000-24,370,001 , GRCh38.p12 chr1: 23,683,510-24,043,511 CNR2, FUCA1, 17 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
    nsv5419917copy number variation1nstd206human GRCh38 chr1: 23,964,009-23,964,170 , GRCh37.p13 chr1: 24,290,499-24,290,660 SRSF10
    nsv5284077copy number variation1nstd204human GRCh38.p13 chr1: 23,963,986-23,964,191 , GRCh37.p13 chr1: 24,290,476-24,290,681 SRSF10
    nsv4903204copy number variation1nstd200human GRCh38 chr1: 23,713,966-24,337,591 , GRCh37.p13 chr1: 24,040,456-24,664,081 , IL22RA1, 25 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
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