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Items: 1 to 20 of 164

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7045923inversion1nstd229human GRCh38 chr2: 24,038,406-24,041,887 , GRCh37.p13 chr2: 24,261,276-24,264,757 FKBP1B, WDCP
    nsv6677204copy number variation1nstd229human GRCh38 chr2: 24,035,314-24,035,344 , GRCh37.p13 chr2: 24,258,184-24,258,214 WDCP, FKBP1B
    nsv6676890copy number variation1nstd229human GRCh38 chr2: 23,963,439-24,043,304 , GRCh37.p13 chr2: 24,186,309-24,266,174 FKBP1B, RN7SL610P, 3 more genes
    nsv6670437copy number variation1nstd229human GRCh38 chr2: 24,035,837-24,042,799 , GRCh37.p13 chr2: 24,258,707-24,265,669 FKBP1B, WDCP
    nsv6666873copy number variation1nstd229human GRCh38 chr2: 23,622,207-24,033,282 , GRCh37.p13 chr2: 23,845,077-24,256,152 SDHCP3, KLHL29, 8 more genes
    nsv6663543copy number variation1nstd229human GRCh38 chr2: 23,871,801-24,132,500 , GRCh37.p13 chr2: 24,094,671-24,355,370 SF3B6, WDCP, 12 more genes
    nsv6637009copy number variation1nstd102humanUncertain significance GRCh37 chr2: 23,908,436-24,636,185 , GRCh38.p12 chr2: 23,685,566-24,413,316 HMGN2P20, KLHL29, 19 more genes
    nsv6636815copy number variation1nstd102humanPathogenic GRCh37 chr2: 706,460-35,523,639 , GRCh38.p12 chr2: 706,460-35,298,573 LOC105374455, RN7SL674P, 504 more genes
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CYP1B1-AS1, LOC107985771, 1649 more genes
    nsv6538978inversion1nstd223human GRCh38 chr2: 24,034,410-24,034,752 , GRCh37.p13 chr2: 24,257,280-24,257,622 FKBP1B, WDCP
    nsv6354916copy number variation1nstd223human GRCh38 chr2: 23,986,421-24,044,996 , GRCh37.p13 chr2: 24,209,291-24,267,866 FKBP1B, MFSD2B, 4 more genes
    nsv6354036copy number variation1nstd223human GRCh38 chr2: 24,034,290-24,035,649 , GRCh37.p13 chr2: 24,257,160-24,258,519 WDCP, FKBP1B
    nsv6353938copy number variation1nstd223human GRCh38 chr2: 24,035,691-24,036,400 , GRCh37.p13 chr2: 24,258,561-24,259,270 FKBP1B, WDCP
    nsv6352331copy number variation1nstd223human GRCh38 chr2: 24,041,613-25,123,987 , GRCh37.p13 chr2: 24,264,483-25,346,856 LOC105377626, ADCY3, 25 more genes
    nsv6342277copy number variation1nstd223human GRCh38 chr2: 24,042,606-24,059,792 , GRCh37.p13 chr2: 24,265,476-24,282,662 WDCP, RNU6-370P, 1 more genes
    nsv6337325copy number variation1nstd223human GRCh38 chr2: 23,963,253-24,089,139 , GRCh37.p13 chr2: 24,186,123-24,312,009 FAM228B, FKBP1B, 7 more genes
    nsv6335995copy number variation1nstd223human GRCh38 chr2: 24,041,200-24,042,570 , GRCh37.p13 chr2: 24,264,070-24,265,440 WDCP, FKBP1B
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6314937copy number variation1nstd102humanPathogenic GRCh37 chr2: 22,439,520-25,608,211 , GRCh38.p12 chr2: 22,216,648-25,385,342 ITSN2, POMC, 50 more genes
    nsv5988332copy number variation1nstd212human GRCh38 chr2: 24,041,355-24,045,335 , GRCh37.p13 chr2: 24,264,225-24,268,205 FKBP1B, WDCP, 1 more genes
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