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Items: 1 to 20 of 942

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148239copy number variation1nstd102humanPathogenic GRCh38 chr13: 98,343,655-110,990,677 , GRCh37.p13 chr13: 98,995,909-111,643,024 CLYBL-AS3, PPIAP24, 162 more genes
    nsv7148164copy number variation1nstd102humanPathogenic GRCh38 chr13: 106,425,676-114,326,445 , GRCh37.p13 chr13: 107,078,024-115,085,141 TUBGCP3, LINC01043, 132 more genes
    nsv7144107insertion1nstd232human GRCh37.p13 chr13: 111,038,087-111,038,087 , GRCh38.p12 chr13: 110,385,740-110,385,740 COL4A2
    nsv7142577insertion1nstd232human GRCh37.p13 chr13: 111,131,743-111,131,743 , GRCh38.p12 chr13: 110,479,396-110,479,396 COL4A2
    nsv7094235copy number variation1nstd102humanUncertain significance GRCh37 chr13: 110,959,271-111,279,914 , GRCh38.p12 chr13: 110,306,924-110,627,567 RAB20, NAXD, 5 more genes
    nsv7093989copy number variation1nstd102humanUncertain significance GRCh37 chr13: 110,822,874-110,960,490 , GRCh38.p12 chr13: 110,170,527-110,308,143 COL4A1, COL4A2
    nsv7074580inversion1nstd229human GRCh38 chr13: 110,243,158-113,630,621 , GRCh37.p13 chr13: 110,895,505-114,284,936 LINC01070, NAXD, 71 more genes
    nsv7062466inversion1nstd229human GRCh38 chr13: 107,288,249-110,580,799 , GRCh37.p13 chr13: 107,940,597-111,233,146 RNA5SP39, MIR1267, 32 more genes
    nsv7060236inversion1nstd229human GRCh38 chr13: 109,400,177-111,221,158 , GRCh37.p13 chr13: 110,052,524-111,873,505 LINC00399, ANKRD10, 36 more genes
    nsv7059605inversion1nstd229human GRCh38 chr13: 110,238,294-111,024,734 , GRCh37.p13 chr13: 110,890,641-111,677,081 COL4A1, RPL21P107, 17 more genes
    nsv6957827copy number variation1nstd229human GRCh38 chr13: 110,400,001-110,889,200 , GRCh37.p13 chr13: 111,052,348-111,541,547 COL4A2-AS2, COL4A2, 12 more genes
    nsv6957375copy number variation1nstd229human GRCh38 chr13: 110,294,204-110,633,816 , GRCh37.p13 chr13: 110,946,551-111,286,163 RAB20, MIR8073, 5 more genes
    nsv6956614copy number variation1nstd229human GRCh38 chr13: 110,319,181-110,321,059 , GRCh37.p13 chr13: 110,971,528-110,973,406 COL4A2
    nsv6956558copy number variation1nstd229human GRCh38 chr13: 110,412,044-110,412,485 , GRCh37.p13 chr13: 111,064,391-111,064,832 COL4A2
    nsv6956195copy number variation1nstd229human GRCh38 chr13: 110,359,201-110,383,700 , GRCh37.p13 chr13: 111,011,548-111,036,047 COL4A2
    nsv6955723copy number variation1nstd229human GRCh38 chr13: 110,387,932-110,394,719 , GRCh37.p13 chr13: 111,040,279-111,047,066 COL4A2
    nsv6954592copy number variation1nstd229human GRCh38 chr13: 110,322,299-111,271,113 , GRCh37.p13 chr13: 110,974,646-111,923,460 ARHGEF7-AS2, LINC00567, 22 more genes
    nsv6953447copy number variation1nstd229human GRCh38 chr13: 110,342,447-110,402,405 , GRCh37.p13 chr13: 110,994,794-111,054,752 COL4A2
    nsv6952764copy number variation1nstd229human GRCh38 chr13: 110,160,401-110,482,000 , GRCh37.p13 chr13: 110,812,748-111,134,347 COL4A1, MIR8073, 2 more genes
    nsv6951490copy number variation1nstd229human GRCh38 chr13: 110,418,901-110,449,100 , GRCh37.p13 chr13: 111,071,248-111,101,447 COL4A2
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