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Items: 1 to 20 of 167

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148056copy number variation1nstd102humanPathogenic GRCh37 chr2: 186,698,504-223,918,111 , GRCh38.p12 chr2: 185,833,777-223,053,393 DNAJB1P1, MTCO2P17, 580 more genes
    nsv7049459inversion1nstd229human GRCh38 chr2: 199,624,566-202,238,851 , GRCh37.p13 chr2: 200,489,289-203,103,574 LOC105373833, NDUFB3, 76 more genes
    nsv6697182copy number variation1nstd229human GRCh38 chr2: 192,562,889-202,434,958 , GRCh37.p13 chr2: 193,427,615-203,299,681 RNU6-915P, SLC44A3P1, 150 more genes
    nsv6691332copy number variation1nstd229human GRCh38 chr2: 201,151,827-201,154,649 , GRCh37.p13 chr2: 202,016,550-202,019,372 CFLAR-AS1, CFLAR
    nsv6686818copy number variation1nstd229human GRCh38 chr2: 201,089,117-201,158,268 , GRCh37.p13 chr2: 201,953,840-202,022,991 RNU7-45P, CFLAR-AS1, 4 more genes
    nsv6678493copy number variation1nstd229human GRCh38 chr2: 201,151,058-201,154,525 , GRCh37.p13 chr2: 202,015,781-202,019,248 CFLAR-AS1, CFLAR
    nsv6637127copy number variation1nstd102humanPathogenic GRCh37 chr2: 189,909,904-209,468,383 , GRCh38.p12 chr2: 189,045,178-208,603,658 LOC100421409, LOC100507443, 310 more genes
    nsv6552662inversion1nstd223human GRCh38 chr2: 201,142,604-201,143,513 , GRCh37.p13 chr2: 202,007,327-202,008,236 CFLAR, CFLAR-AS1
    nsv6315398copy number variation1nstd102humanPathogenic GRCh37 chr2: 185,697,659-213,002,074 , GRCh38.p12 chr2: 184,832,932-212,137,349 LOC107985785, MYO1B, 381 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6315388copy number variation1nstd102humanUncertain significance GRCh37 chr2: 201,838,259-202,711,243 , GRCh38.p12 chr2: 200,973,536-201,846,520 MTND4LP13, SCYL2P1, 36 more genes
    nsv6313730copy number variation1nstd102humanPathogenic GRCh37 chr2: 200,851,079-209,054,267 , GRCh38.p12 chr2: 199,986,356-208,189,543 RN7SKP200, PIMREGP1, 179 more genes
    nsv6311365copy number variation5nstd102humanUncertain significance, Pathogenic GRCh37 chr2: 201,943,606-204,824,322 , GRCh38.p12 chr2: 201,078,883-203,959,599 MTND4LP17, SNORD11, 87 more genes
    nsv6134530copy number variation1nstd213human GRCh37 chr2: 201,780,000-202,780,001 , GRCh38.p12 chr2: 200,915,277-201,915,278 CASP8, CASP10, 37 more genes
    nsv5831846copy number variation1nstd209human GRCh38 chr2: 201,135,967-201,139,854 , GRCh37.p13 chr2: 202,000,690-202,004,577 CFLAR, IMPDH1P10, 1 more genes
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5445534copy number variation1nstd206human GRCh38 chr2: 201,143,395-201,156,199 , GRCh37.p13 chr2: 202,008,118-202,020,922 CFLAR, CFLAR-AS1
    nsv4910327copy number variation1nstd200human GRCh38 chr2: 201,151,058-201,154,519 , GRCh37.p13 chr2: 202,015,781-202,019,242 CFLAR-AS1, CFLAR
    nsv4728725copy number variation1nstd102humanPathogenic GRCh37 chr2: 178,397,959-243,007,457 , GRCh38.p12 chr2: 177,533,231-242,065,306 LOC105376755, FZD7, 1013 more genes
    nsv4728199copy number variation1nstd102humanUncertain significance GRCh37 chr2: 202,011,822-202,749,788 , GRCh38.p12 chr2: 201,147,099-201,885,065 MTCO1P16, CFLAR, 26 more genes
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