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Items: 1 to 20 of 143

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7067508inversion1nstd229human GRCh38 chr8: 51,755,366-56,976,322 , GRCh37.p13 chr8: 52,667,926-57,888,881 CHCHD2P10, LOC105375850, 81 more genes
    nsv7064051inversion1nstd229human GRCh38 chr8: 53,370,406-56,357,942 , GRCh37.p13 chr8: 54,282,966-57,270,501 CHCHD2P10, RN7SL798P, 51 more genes
    nsv6857941copy number variation1nstd229human GRCh38 chr8: 55,411,549-55,698,605 , GRCh37.p13 chr8: 56,324,109-56,611,164 LOC105375845, LOC105375846, 3 more genes
    nsv6850697copy number variation1nstd229human GRCh38 chr8: 55,454,401-55,458,300 , GRCh37.p13 chr8: 56,366,961-56,370,860 SBF1P1, XKR4
    nsv6849745copy number variation1nstd229human GRCh38 chr8: 55,444,792-55,450,516 , GRCh37.p13 chr8: 56,357,352-56,363,076 SBF1P1, XKR4
    nsv6848642copy number variation1nstd229human GRCh38 chr8: 55,452,756-55,453,136 , GRCh37.p13 chr8: 56,365,316-56,365,696 SBF1P1, XKR4
    nsv6847992copy number variation1nstd229human GRCh38 chr8: 54,863,026-55,486,960 , GRCh37.p13 chr8: 55,775,586-56,399,520 SBF1P1, LOC107986887, 4 more genes
    nsv6844062copy number variation1nstd229human GRCh38 chr8: 55,441,911-55,447,800 , GRCh37.p13 chr8: 56,354,471-56,360,360 SBF1P1, XKR4
    nsv6569954inversion1nstd223human GRCh38 chr8: 50,962,824-58,188,676 , GRCh37.p13 chr8: 51,875,384-59,101,235 LOC101929398, LOC107986888, 98 more genes
    nsv6427839copy number variation1nstd223human GRCh38 chr8: 55,455,101-55,455,500 , GRCh37.p13 chr8: 56,367,661-56,368,060 XKR4, SBF1P1
    nsv6136681copy number variation1nstd213human GRCh37 chr8: 46,860,000-86,550,001 , GRCh38.p12 chr8: 45,948,378-85,637,772 CEBPD, EYA1, 519 more genes
    nsv6136061copy number variation1nstd213human GRCh37 chr8: 54,780,000-63,060,001 , GRCh38.p12 chr8: 53,867,440-62,147,442 RAB2A, SDCBP, 117 more genes
    nsv5956782insertion1nstd209human GRCh38 chr8: 55,454,148-55,454,148 , GRCh37.p13 chr8: 56,366,708-56,366,708 XKR4, SBF1P1
    nsv5713206mobile element insertion2nstd211human GRCh38 chr8: 55,454,162-55,454,162 , GRCh37.p13 chr8: 56,366,722-56,366,722 XKR4, SBF1P1
    nsv5403042mobile element insertion1nstd206human GRCh38 chr8: 55,454,162-55,454,213 , GRCh37.p13 chr8: 56,366,722-56,366,773 XKR4, SBF1P1
    nsv5106351mobile element insertion1nstd203human GRCh38 chr8: 55,454,148-55,454,162 , GRCh37.p13 chr8: 56,366,708-56,366,722 XKR4, SBF1P1
    nsv4683142copy number variation1nstd102humanUncertain significance GRCh37 chr8: 54,978,308-56,436,786 , GRCh38.p12 chr8: 54,065,748-55,524,227 XKR4, LOC105375844, 21 more genes
    nsv4485796mobile element insertion1nstd166human GRCh37.p13 chr8: 56,366,708-56,366,708 , GRCh38.p12 chr8: 55,454,148-55,454,148 SBF1P1, XKR4
    nsv4456871copy number variation1nstd102humanPathogenic GRCh37 chr8: 39,555,657-64,049,089 , GRCh38.p12 chr8: 39,698,138-63,136,530 CRIPTOP5, TRIM60P15, 297 more genes
    nsv4456811copy number variation1nstd102humanPathogenic GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385 TERF1, LOC107986945, 1511 more genes
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