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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3870867copy number variation1nstd102humanUncertain significance GRCh37 chr1: 231,828,116-231,928,554 , GRCh38.p12 chr1: 231,692,370-231,792,808 DISC1, TSNAX-DISC1
    nsv3874891copy number variation1nstd102humanLikely pathogenic GRCh38 chr1: 231,740,970-231,949,671 , GRCh37.p13 chr1: 231,876,716-232,085,417 DISC2, DISC1, 3 more genes
    nsv3878194copy number variation1nstd102humanBenign GRCh37 chr1: 231,709,404-231,813,134 , GRCh38.p12 chr1: 231,573,658-231,677,388 DISC1, RNU5A-5P, 2 more genes
    nsv3887735copy number variation1nstd102humanBenign GRCh37 chr1: 231,710,352-231,813,921 , GRCh38.p12 chr1: 231,574,606-231,678,175 LINC00582, DISC1, 2 more genes
    nsv3883873copy number variation1nstd102humanBenign GRCh37 chr1: 231,711,622-231,813,134 , GRCh38.p12 chr1: 231,575,876-231,677,388 DISC1, TSNAX-DISC1, 2 more genes
    nsv3908079copy number variation1nstd102humanBenign/Likely benign GRCh38 chr1: 231,579,387-231,678,175 , GRCh37 chr1: 231,715,133-231,813,921 , NCBI36 chr1: 229,781,756-229,880,544 DISC1, RNU5A-5P, 2 more genes
    nsv3896793copy number variation1nstd102humanLikely benign NCBI36 chr1: 229,816,289-229,880,603 , GRCh38 chr1: 231,613,920-231,678,234 , GRCh37 chr1: 231,749,666-231,813,980 TSNAX-DISC1, DISC1, 1 more genes
    nsv3886871copy number variation1nstd102humanBenign GRCh37 chr1: 232,074,973-232,121,222 , GRCh38.p12 chr1: 231,939,227-231,985,476 TSNAX-DISC1, DISC1-IT1, 1 more genes
    nsv6290368copy number variation1nstd102humanUncertain significance GRCh37 chr1: 231,908,212-232,027,911 , GRCh38.p12 chr1: 231,772,466-231,892,165 TSNAX-DISC1, DISC2, 2 more genes
    nsv6636472copy number variation1nstd102humanUncertain significance GRCh37 chr1: 231,859,872-231,966,836 , GRCh38.p12 chr1: 231,724,126-231,831,090 DISC1, LOC105373170, 2 more genes
    nsv3897606copy number variation1nstd102humanUncertain significance NCBI36 chr1: 230,152,662-230,259,407 , GRCh38 chr1: 231,950,293-232,057,038 , GRCh37 chr1: 232,086,039-232,192,784 LOC105373171, LOC105373172, 2 more genes
    nsv3915050copy number variation1nstd102humanUncertain significance NCBI36 chr1: 230,139,624-230,212,533 , GRCh37.p13 chr1: 232,073,001-232,145,910 , GRCh38.p12 chr1: 231,937,255-232,010,164 DISC1, TSNAX-DISC1, 1 more genes
    nsv3889287copy number variation1nstd102humanUncertain significance GRCh37 chr1: 231,908,346-231,943,836 , GRCh38.p12 chr1: 231,772,600-231,808,090 DISC1, LOC105373170, 1 more genes
    nsv6290413copy number variation1nstd102humanUncertain significance GRCh37 chr1: 231,922,558-231,943,836 , GRCh38.p12 chr1: 231,786,812-231,808,090 TSNAX-DISC1, DISC1, 1 more genes
    nsv4674424copy number variation1nstd102humanUncertain significance GRCh37 chr1: 231,763,761-232,045,506 , GRCh38.p12 chr1: 231,628,015-231,909,760 RNU5A-5P, LOC105373170, 3 more genes
    nsv4674109copy number variation1nstd102humanUncertain significance GRCh37 chr1: 231,788,026-232,045,506 , GRCh38.p12 chr1: 231,652,280-231,909,760 LOC105373170, DISC2, 3 more genes
    nsv3877481copy number variation1nstd102humannot provided GRCh38 chr1: 231,573,658-231,727,458 , GRCh37 chr1: 231,709,404-231,863,204 TSNAX-DISC1, RNU5A-5P, 2 more genes
    nsv4674001copy number variation1nstd102humanUncertain significance GRCh37 chr1: 232,067,056-232,204,833 , GRCh38.p12 chr1: 231,931,310-232,069,087 DISC1, LOC105373172, 3 more genes
    nsv3883963copy number variation1nstd102humannot provided GRCh37 chr1: 231,709,404-231,813,134 , GRCh38 chr1: 231,573,658-231,677,388 TSNAX-DISC1, LINC00582, 2 more genes
    nsv3874733copy number variation1nstd102humanUncertain significance GRCh37 chr1: 231,713,096-231,816,223 , GRCh38.p12 chr1: 231,577,350-231,680,477 LINC00582, TSNAX-DISC1, 2 more genes
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