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Items: 1 to 20 of 29

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3903382copy number variation1nstd102humanBenign GRCh37 chr7: 107,960,937-108,027,226 , GRCh38.p12 chr7: 108,320,493-108,386,782 NRCAM
    nsv4729293copy number variation1nstd102humanUncertain significance GRCh37 chr7: 108,025,055-108,085,810 , GRCh38.p12 chr7: 108,384,611-108,445,366 NRCAM
    nsv3883798copy number variation1nstd102humannot provided GRCh38 chr7: 108,418,130-108,425,882 , GRCh37 chr7: 108,058,574-108,066,326 NRCAM
    esv3648374copy number variation1estd216humannot provided GRCh37 chr7: 108,058,574-108,066,326 , GRCh38.p12 chr7: 108,418,130-108,425,882 NRCAM
    nsv3919826copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840 NRCAM, RNU6-438P, 2682 more genes
    nsv3888815copy number variation1nstd102humanPathogenic GRCh37 chr7: 12,258,147-140,494,267 , GRCh38.p12 chr7: 12,218,521-140,794,467 NRCAM, LOC107986817, 2014 more genes
    nsv3924380copy number variation1nstd102humanPathogenic GRCh37 chr7: 101,912,320-120,918,695 , GRCh38 chr7: 102,196,924-121,278,641 , NCBI36 chr7: 101,626,924-120,705,931 NRCAM, LOC102724434, 222 more genes
    nsv6313576copy number variation1nstd102humanPathogenic GRCh37 chr7: 100,676,872-119,156,160 , GRCh38.p12 chr7: 101,033,591-119,516,106 NRCAM, LHFPL3-AS2, 233 more genes
    nsv4675322copy number variation1nstd102humanPathogenic GRCh37 chr7: 106,617,406-123,217,914 , GRCh38.p12 chr7: 106,976,961-123,577,860 NRCAM, CBLL1-AS1, 168 more genes
    nsv3923570copy number variation1nstd102humanPathogenic NCBI36 chr7: 107,583,881-122,963,817 , GRCh37.p13 chr7: 107,796,645-123,176,581 , GRCh38.p12 chr7: 108,156,200-123,536,527 NRCAM, ANKRD7, 142 more genes
    nsv6313503copy number variation1nstd102humanPathogenic GRCh37 chr7: 99,417,471-111,586,308 , GRCh38.p12 chr7: 99,819,848-111,946,253 NRCAM, GJC3, 237 more genes
    nsv3912378copy number variation1nstd102humanPathogenic GRCh38 chr7: 101,807,149-112,414,850 , GRCh37 chr7: 101,450,429-112,054,905 , NCBI36 chr7: 101,237,149-111,842,141 NRCAM, DNAJC2, 139 more genes
    nsv4455557copy number variation1nstd102humanPathogenic GRCh37 chr7: 107,410,314-117,825,549 , GRCh38.p12 chr7: 107,769,869-118,185,495 NRCAM, RAC1P6, 103 more genes
    nsv3913401copy number variation1nstd102humanPathogenic GRCh37 chr7: 105,902,385-110,868,092 , GRCh38 chr7: 106,261,939-111,228,036 , NCBI36 chr7: 105,689,621-110,655,328 NRCAM, DUS4L-BCAP29, 52 more genes
    nsv3913409copy number variation1nstd102humanPathogenic NCBI36 chr7: 107,600,493-111,402,206 , GRCh37.p13 chr7: 107,813,257-111,614,970 , GRCh38.p12 chr7: 108,172,812-111,974,915 NRCAM, RNU7-83P, 24 more genes
    nsv7097853copy number variation1nstd102humanPathogenic GRCh37 chr7: 104,456,677-108,155,935 , GRCh38.p12 chr7: 104,816,230-108,515,491 NRCAM, RNU6-1322P, 57 more genes
    nsv3894780copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,704-159,122,532 , GRCh38.p12 chr7: 10,704-159,329,842 NRCAM, RNU6-565P, 2684 more genes
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 NRCAM, RPL23AP51, 2684 more genes
    nsv3909087copy number variation1nstd102humanPathogenic GRCh37 chr7: 44,935-159,126,310 , GRCh38.p12 chr7: 44,935-159,333,620 NRCAM, MNX1-AS2, 2682 more genes
    nsv3908592copy number variation2nstd102humanPathogenic GRCh37 chr7: 43,361-159,119,707 , GRCh38.p12 chr7: 43,361-159,327,017 NRCAM, TRGV3, 2682 more genes
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