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Items: 1 to 20 of 195

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098787copy number variation1nstd102humanUncertain significance GRCh37 chr6: 32,148,920-36,953,949 , GRCh38.p12 chr6: 32,181,143-36,986,173 CUTA, SYNGAP1, 184 more genes
    nsv7097426copy number variation1nstd102humanUncertain significance GRCh37 chr6: 30,695,893-36,953,949 , GRCh38.p12 chr6: 30,728,116-36,986,173 LEMD2, PSORS1C1, 321 more genes
    nsv7053830inversion1nstd229human GRCh38 chr6: 29,164,448-38,692,657 , GRCh37.p13 chr6: 29,132,225-38,660,433 GTF2H4, RNF8, 472 more genes
    nsv7045112inversion1nstd229human GRCh38 chr6: 30,561,326-37,907,708 , GRCh37.p13 chr6: 30,529,103-37,875,484 ZBTB22, PNPLA1, 355 more genes
    nsv7038851inversion1nstd229human GRCh38 chr6: 32,132,840-33,082,625 , GRCh37.p13 chr6: 32,100,617-33,050,402 TAP1, LOC100294145, 48 more genes
    nsv6788814copy number variation1nstd229human GRCh38 chr6: 32,184,574-32,184,643 , GRCh37.p13 chr6: 32,152,351-32,152,420 PBX2, AGER
    nsv6779807copy number variation1nstd229human GRCh38 chr6: 31,800,134-32,311,768 , GRCh37.p13 chr6: 31,767,911-32,279,545 NELFE, CYP21A1P, 43 more genes
    nsv6402266copy number variation1nstd223human GRCh38 chr6: 31,522,086-32,653,908 , GRCh37.p13 chr6: 31,489,863-32,621,685 MIR6833, LY6G5B, 102 more genes
    nsv6169943copy number variation1nstd214human GRCh38 chr6: 32,184,580-32,184,642 , GRCh37.p13 chr6: 32,152,357-32,152,419 AGER, PBX2
    nsv6135917copy number variation1nstd213human GRCh37 chr6: 30,110,000-32,450,001 , GRCh38.p12 chr6: 30,142,223-32,482,224 ABCF1, AGER, 186 more genes
    nsv6009216copy number variation1nstd212human GRCh38 chr6: 32,184,580-32,184,643 , GRCh37.p13 chr6: 32,152,357-32,152,420 PBX2, AGER
    nsv5890393copy number variation1nstd209human GRCh38 chr6: 32,184,580-32,184,642 , GRCh37.p13 chr6: 32,152,357-32,152,419 PBX2, AGER
    nsv5566913copy number variation1nstd207human GRCh38 chr6: 32,184,580-32,184,642 , GRCh37.p13 chr6: 32,152,357-32,152,419 PBX2, AGER
    nsv5473905copy number variation1nstd206human GRCh38 chr6: 32,184,584-32,184,643 , GRCh37.p13 chr6: 32,152,361-32,152,420 AGER, PBX2
    nsv5362819translocation1nstd200human GRCh38 chr6: 32,184,584-32,184,584 , GRCh38 chr6: 32,184,643-32,184,643 , GRCh37.p13 chr6: 32,152,361-32,152,361 , GRCh37.p13 chr6: 32,152,420-32,152,420 PBX2, AGER
    nsv5320521translocation1nstd204human GRCh37.p13 chr6: 32,152,361-32,152,361 , GRCh37.p13 chr6: 32,152,420-32,152,420 , GRCh38.p13 chr6: 32,184,584-32,184,584 , GRCh38.p13 chr6: 32,184,643-32,184,643 AGER, PBX2
    nsv5234405copy number variation1nstd204human GRCh38.p13 chr6: 30,240,001-32,313,700 , GRCh37.p13 chr6: 30,207,778-32,281,477 DDAH2, LOC105375018, 175 more genes
    nsv5231391copy number variation1nstd204human GRCh37.p13 chr6: 32,145,178-32,165,377 , GRCh38.p13 chr6: 32,177,401-32,197,600 AGER, NOTCH4, 5 more genes
    nsv4757608inversion1nstd199human GRCh37 chr6: 26,743,921-58,149,359 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4756329inversion1nstd199human GRCh37 chr6: 26,745,246-58,149,317 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
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