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Items: 1 to 20 of 936

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076885inversion1nstd229human GRCh38 chr22: 22,166,804-22,475,762 , GRCh37.p13 chr22: 22,521,197-22,830,099 LOC105372952, IGLV1-51, 37 more genes
    nsv7035422copy number variation1nstd229human GRCh38 chr22: 22,196,346-22,918,168 , GRCh37.p13 chr22: 22,550,746-23,260,340 IGLJ4, IGLV1-41, 98 more genes
    nsv7028727copy number variation1nstd229human GRCh38 chr22: 22,371,661-22,381,863 , GRCh37.p13 chr22: 22,726,029-22,736,232 IGL, IGLV1-44, 1 more genes
    nsv7022030copy number variation1nstd229human GRCh38 chr22: 22,362,840-22,389,038 , GRCh37.p13 chr22: 22,717,200-22,743,406 IGLV7-46, IGLV5-45, 3 more genes
    nsv7020052copy number variation1nstd229human GRCh38 chr22: 22,357,755-22,380,757 , GRCh37.p13 chr22: 22,712,103-22,735,126 ASH2LP2, IGL, 4 more genes
    nsv6637335copy number variation1nstd102humanPathogenic GRCh37 chr22: 21,465,662-22,962,962 , GRCh38.p12 chr22: 21,111,373-22,620,492 ABHD17AP5, UBE2L3, 97 more genes
    nsv6627184copy number variation1nstd224human GRCh37 chr22: 21,799,719-23,803,722 , GRCh38.p12 chr22: 21,445,430-23,461,535 BCRP4, GNAZ, 158 more genes
    nsv6552430copy number variation1nstd223human GRCh38 chr22: 22,376,361-22,899,720 , GRCh37.p13 chr22: 22,730,730-23,241,900 ZNF280B, IGLVI-20, 69 more genes
    nsv6551420copy number variation1nstd223human GRCh38 chr22: 22,099,252-22,905,006 , GRCh37.p13 chr22: 22,453,662-23,247,186 IGLJ3, BCRP4, 99 more genes
    nsv6546953copy number variation1nstd223human GRCh38 chr22: 22,369,797-22,395,199 , GRCh37.p13 chr22: 22,724,165-22,749,537 IGL, IGLVI-42, 4 more genes
    nsv6540095copy number variation1nstd223human GRCh38 chr22: 20,268,331-23,402,807 , GRCh37.p13 chr22: 20,255,854-23,744,994 IGLC2, IGLVIV-53, 214 more genes
    nsv6540089copy number variation1nstd223human GRCh38 chr22: 22,322,194-22,403,946 , GRCh37.p13 chr22: 22,676,550-22,758,278 IGLVVII-41-1, IGLV1-41, 15 more genes
    nsv6539336copy number variation1nstd223human GRCh38 chr22: 22,362,840-22,389,038 , GRCh37.p13 chr22: 22,717,200-22,743,406 IGLV1-44, IGLV5-45, 3 more genes
    nsv6315562copy number variation1nstd102humanPathogenic GRCh37 chr22: 21,798,906-25,039,018 , GRCh38.p12 chr22: 21,444,617-24,643,051 IGLVI-42, ADORA2A-AS1, 205 more genes
    nsv6315480copy number variation1nstd102humanPathogenic GRCh37 chr22: 21,462,566-22,962,196 , GRCh38.p12 chr22: 21,108,277-22,619,726 IGLV8-61, SDF2L1, 97 more genes
    nsv6314782copy number variation1nstd220human GRCh38.p12 chr22: 21,351,861-24,248,764 , GRCh37 chr22: 21,706,150-24,644,732 ASLP1, BCR, 195 more genes
    nsv6306831copy number variation1nstd186human GRCh37 chr22: 22,453,601-23,235,888 , GRCh38.p12 chr22: 22,099,191-22,893,708 , IGLV2-14, 97 more genes
    nsv6305929copy number variation1nstd186human GRCh37 chr22: 22,724,451-23,247,171 , GRCh38.p12 chr22: 22,370,083-22,904,991 , IGLV1-41, 74 more genes
    nsv6291464copy number variation1nstd102humanPathogenic GRCh37 chr22: 21,465,661-24,631,791 , GRCh38.p12 chr22: 21,111,372-24,235,823 IGLVIV-64, FAM230B, 205 more genes
    nsv6290344copy number variation1nstd102humanUncertain significance GRCh37 chr22: 21,905,051-22,989,041 , GRCh38.p12 chr22: 21,550,762-22,646,571 IGLV1-47, LOC100736408, 81 more genes
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