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Items: 1 to 20 of 377

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7141354insertion1nstd232human GRCh37.p13 chr1: 52,269,636-52,269,636 , GRCh38.p12 chr1: 51,803,964-51,803,964 NRDC
    nsv7140853insertion1nstd232human GRCh37.p13 chr1: 52,266,355-52,266,355 , GRCh38.p12 chr1: 51,800,683-51,800,683 NRDC
    nsv7138398copy number variation1nstd232human GRCh37.p13 chr1: 52,280,279-52,280,361 , GRCh38.p12 chr1: 51,814,607-51,814,689 NRDC
    nsv7099204copy number variation1nstd231human GRCh38.p12 chr1: 51,433,462-53,162,521 , GRCh37 chr1: 51,899,134-53,628,193 EPS15, GPX7, 53 more genes
    nsv7052650inversion1nstd229human GRCh38 chr1: 47,584,744-54,395,558 , GRCh37.p13 chr1: 48,050,416-54,861,231 ANAPC10P1, SPATA6, 137 more genes
    nsv7038227inversion1nstd229human GRCh38 chr1: 51,791,034-51,793,436 , GRCh37.p13 chr1: 52,256,706-52,259,108 NRDC
    nsv6651626copy number variation1nstd229human GRCh38 chr1: 51,861,909-51,866,341 , GRCh37.p13 chr1: 52,327,581-52,332,013 NRDC
    nsv6651625copy number variation1nstd229human GRCh38 chr1: 51,840,671-51,843,036 , GRCh37.p13 chr1: 52,306,343-52,308,708 NRDC
    nsv6651540copy number variation1nstd229human GRCh38 chr1: 51,849,665-51,850,010 , GRCh37.p13 chr1: 52,315,337-52,315,682 NRDC
    nsv6651539copy number variation1nstd229human GRCh38 chr1: 51,846,690-51,852,321 , GRCh37.p13 chr1: 52,312,362-52,317,993 NRDC
    nsv6651538copy number variation1nstd229human GRCh38 chr1: 51,812,640-52,176,504 , GRCh37.p13 chr1: 52,278,312-52,642,176 MIR761, RAB3B, 14 more genes
    nsv6651408copy number variation1nstd229human GRCh38 chr1: 51,857,185-51,861,275 , GRCh37.p13 chr1: 52,322,857-52,326,947 NRDC, TSEN15P2
    nsv6651406copy number variation1nstd229human GRCh38 chr1: 51,842,000-51,844,613 , GRCh37.p13 chr1: 52,307,672-52,310,285 NRDC
    nsv6651404copy number variation1nstd229human GRCh38 chr1: 51,762,101-51,802,200 , GRCh37.p13 chr1: 52,227,773-52,267,872 NRDC, OSBPL9
    nsv6651403copy number variation1nstd229human GRCh38 chr1: 51,700,001-52,215,600 , GRCh37.p13 chr1: 52,165,673-52,681,272 TXNDC12, MIR761, 19 more genes
    nsv6651389copy number variation1nstd229human GRCh38 chr1: 51,393,525-52,345,796 , GRCh37.p13 chr1: 51,859,197-52,811,468 SLC25A6P3, LOC724060, 26 more genes
    nsv6651312copy number variation1nstd229human GRCh38 chr1: 51,780,067-51,838,569 , GRCh37.p13 chr1: 52,245,739-52,304,241 OSBPL9, MIR761, 1 more genes
    nsv6638064copy number variation1nstd102humanassociation GRCh38 chr1: 48,666,286-52,808,894 , GRCh37.p13 chr1: 49,131,958-53,274,566 LOC105378710, RNU6-1026P, 80 more genes
    nsv6636580copy number variation1nstd102humanUncertain significance GRCh37 chr1: 51,797,643-52,256,345 , GRCh38.p12 chr1: 51,331,971-51,790,673 RNU6-877P, LOC105378719, 10 more genes
    nsv6551737inversion1nstd223human GRCh38 chr1: 51,845,451-51,846,164 , GRCh37.p13 chr1: 52,311,123-52,311,836 NRDC
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