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Items: 1 to 20 of 31

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3878119copy number variation1nstd102humanBenign GRCh37 chr4: 96,240,018-96,255,088 , GRCh38.p12 chr4: 95,318,867-95,333,937 UNC5C
    nsv3872131copy number variation1nstd102humanBenign GRCh37 chr4: 96,246,506-96,247,348 , GRCh38.p12 chr4: 95,325,355-95,326,197 UNC5C
    nsv3883032copy number variation1nstd102humanBenign GRCh37 chr4: 96,246,695-96,247,498 , GRCh38.p12 chr4: 95,325,544-95,326,347 UNC5C
    nsv3972183copy number variation1nstd102humanLikely benign GRCh37 chr4: 95,987,699-96,171,863 , GRCh38.p12 chr4: 95,066,548-95,250,712 UNC5C, BMPR1B
    nsv3913596copy number variation1nstd102humanUncertain significance NCBI36 chr4: 96,042,147-96,347,350 , GRCh37 chr4: 95,823,124-96,128,327 , GRCh38 chr4: 94,901,973-95,207,176 UNC5C, BMPR1B
    nsv4456870copy number variation1nstd102humanUncertain significance GRCh37 chr4: 96,059,519-96,361,153 , GRCh38.p12 chr4: 95,138,368-95,440,002 UNC5C, BMPR1B
    nsv3874481copy number variation1nstd102humanUncertain significance GRCh37 chr4: 95,975,469-96,181,052 , GRCh38.p12 chr4: 95,054,318-95,259,901 UNC5C, BMPR1B
    nsv3916742copy number variation1nstd102humanLikely benign NCBI36 chr4: 95,720,284-96,328,830 , GRCh38 chr4: 94,580,110-95,188,656 , GRCh37 chr4: 95,501,261-96,109,807 UNC5C, BMPR1B-DT, 2 more genes
    nsv3884602copy number variation1nstd102humanLikely benign GRCh37 chr4: 95,492,115-96,091,575 , GRCh38.p12 chr4: 94,570,964-95,170,424 UNC5C, PDLIM5, 2 more genes
    nsv4684259copy number variation1nstd102humanUncertain significance GRCh37 chr4: 96,376,995-96,828,109 , GRCh38.p12 chr4: 95,455,844-95,906,958 UNC5C, UNC5C-AS1, 3 more genes
    nsv3913203copy number variation1nstd102humanUncertain significance GRCh38 chr4: 94,616,498-95,446,867 , GRCh37 chr4: 95,537,649-96,368,018 , NCBI36 chr4: 95,756,672-96,587,041 UNC5C, PDLIM5, 2 more genes
    nsv4456972copy number variation1nstd102humanUncertain significance GRCh37 chr4: 95,732,136-96,494,451 , GRCh38.p12 chr4: 94,810,985-95,573,300 UNC5C, BMPR1B, 1 more genes
    nsv3923759copy number variation1nstd102humanPathogenic NCBI36 chr4: 58,862,002-102,129,682 , GRCh37.p13 chr4: 59,167,245-101,910,659 , GRCh38.p12 chr4: 58,301,079-100,989,502 UNC5C, EREG, 530 more genes
    nsv3923733copy number variation1nstd102humanPathogenic GRCh38 chr4: 80,427,023-100,855,441 , GRCh37 chr4: 81,348,177-101,776,598 , NCBI36 chr4: 81,567,201-101,995,621 UNC5C, PDLIM5, 215 more genes
    nsv7148241copy number variation1nstd102humanPathogenic GRCh38 chr4: 79,123,548-99,457,773 , GRCh37.p13 chr4: 80,044,702-100,378,930 UNC5C, LOC105377327, 214 more genes
    nsv3888958copy number variation1nstd102humanPathogenic GRCh37 chr4: 81,314,915-96,636,651 , GRCh38.p12 chr4: 80,393,761-95,715,500 UNC5C, LOC391674, 156 more genes
    nsv3885328copy number variation1nstd102humanPathogenic GRCh37 chr4: 92,201,567-103,043,808 , GRCh38.p12 chr4: 91,280,416-102,122,651 UNC5C, TRMT10A, 86 more genes
    nsv3910689copy number variation1nstd102humanPathogenic GRCh38 chr4: 92,610,413-101,521,991 , GRCh37 chr4: 93,531,564-102,443,148 , NCBI36 chr4: 93,750,587-102,662,171 UNC5C, GRID2, 77 more genes
    nsv3888291copy number variation1nstd102humanPathogenic GRCh37 chr4: 90,005,204-96,971,785 , GRCh38.p12 chr4: 89,084,053-96,050,634 UNC5C, HMGB3P15, 33 more genes
    nsv3873978copy number variation1nstd102humanPathogenic GRCh37 chr4: 11,525-191,028,879 , GRCh38.p12 chr4: 11,525-190,107,724 UNC5C, LOC100422029, 2358 more genes
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