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Items: 1 to 20 of 277

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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
    nsv6696612copy number variation1nstd229human GRCh38 chr2: 201,067,901-201,120,900 , GRCh37.p13 chr2: 201,932,624-201,985,623 RNU6-1206P, RPL17P10, 4 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
    nsv6689413copy number variation1nstd229human GRCh38 chr2: 201,173,992-201,179,951 , GRCh37.p13 chr2: 202,038,715-202,044,674 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
    nsv6681242copy number variation1nstd229human GRCh38 chr2: 201,105,692-201,115,147 , GRCh37.p13 chr2: 201,970,415-201,979,870 CFLAR, LOC105373836
    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
    nsv6347739copy number variation1nstd223human GRCh38 chr2: 201,173,375-201,173,838 , GRCh37.p13 chr2: 202,038,098-202,038,561 CFLAR
    nsv6340134copy number variation1nstd223human GRCh38 chr2: 201,115,401-201,118,100 , GRCh37.p13 chr2: 201,980,124-201,982,823 LOC105373836, CFLAR
    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
    nsv6298205copy number variation1nstd186human GRCh37 chr2: 201,997,857-202,000,692 , GRCh38.p12 chr2: 201,133,134-201,135,969 IMPDH1P10, CFLAR
    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
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