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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7051393inversion1nstd229human GRCh38 chr2: 101,323,195-101,457,050 , GRCh37.p13 chr2: 101,939,657-102,073,512 CREG2, RFX8, 1 more genes
    nsv6695770copy number variation1nstd229human GRCh38 chr2: 101,102,526-102,065,468 , GRCh37.p13 chr2: 101,718,988-102,681,928 LOC107985789, PRCPP1, 17 more genes
    nsv6695585copy number variation1nstd229human GRCh38 chr2: 101,416,374-101,431,448 , GRCh37.p13 chr2: 102,032,836-102,047,910 RFX8
    nsv6693600copy number variation1nstd229human GRCh38 chr2: 101,469,365-101,474,443 , GRCh37.p13 chr2: 102,085,827-102,090,905 RFX8
    nsv6691881copy number variation1nstd229human GRCh38 chr2: 101,410,209-101,410,264 , GRCh37.p13 chr2: 102,026,671-102,026,726 RFX8
    nsv6691684copy number variation1nstd229human GRCh38 chr2: 101,452,978-101,453,150 , GRCh37.p13 chr2: 102,069,440-102,069,612 RFX8
    nsv6687625copy number variation1nstd229human GRCh38 chr2: 101,398,735-101,400,851 , GRCh37.p13 chr2: 102,015,197-102,017,313 RFX8
    nsv6687279copy number variation1nstd229human GRCh38 chr2: 101,279,320-101,725,723 , GRCh37.p13 chr2: 101,895,782-102,342,185 MIR5696, LOC105373512, 9 more genes
    nsv6686856copy number variation1nstd229human GRCh38 chr2: 101,422,425-101,426,827 , GRCh37.p13 chr2: 102,038,887-102,043,289 RFX8
    nsv6685895copy number variation1nstd229human GRCh38 chr2: 101,474,709-101,475,492 , GRCh37.p13 chr2: 102,091,171-102,091,954 RFX8
    nsv6685861copy number variation1nstd229human GRCh38 chr2: 101,419,904-101,424,844 , GRCh37.p13 chr2: 102,036,366-102,041,306 RFX8
    nsv6680278copy number variation1nstd229human GRCh38 chr2: 101,402,960-101,403,480 , GRCh37.p13 chr2: 102,019,422-102,019,942 RFX8
    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
    nsv6352542copy number variation1nstd223human GRCh38 chr2: 101,403,635-101,408,312 , GRCh37.p13 chr2: 102,020,097-102,024,774 RFX8
    nsv6352519copy number variation1nstd223human GRCh38 chr2: 101,465,458-101,468,259 , GRCh37.p13 chr2: 102,081,920-102,084,721 RFX8
    nsv6341951copy number variation1nstd223human GRCh38 chr2: 101,439,783-101,441,240 , GRCh37.p13 chr2: 102,056,245-102,057,702 RFX8
    nsv6340248copy number variation1nstd223human GRCh38 chr2: 101,398,735-101,400,845 , GRCh37.p13 chr2: 102,015,197-102,017,307 RFX8
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6314726copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196 ACTG2, ACYP2, 1713 more genes
    nsv6299004copy number variation1nstd186human GRCh37 chr2: 102,019,462-102,148,080 , GRCh38.p12 chr2: 101,403,000-101,531,618 RPS6P3, RFX8, 2 more genes
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