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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3917844copy number variation1nstd102humanLikely benign GRCh38 chr7: 88,789,989-89,802,049 , GRCh37 chr7: 88,419,303-89,431,363 , NCBI36 chr7: 88,257,239-89,269,299 TEX47, ZNF804B, 3 more genes
    nsv3911988copy number variation1nstd102humanLikely benign GRCh37 chr7: 88,407,067-89,242,492 , GRCh38 chr7: 88,777,753-89,613,178 , NCBI36 chr7: 88,245,003-89,080,428 TEX47, LOC105375387, 2 more genes
    nsv3890194copy number variation1nstd102humanBenign GRCh37 chr7: 88,410,013-89,244,814 , GRCh38.p12 chr7: 88,780,699-89,615,500 TEX47, LOC107986817, 2 more genes
    nsv3903600copy number variation1nstd102humanUncertain significance GRCh37 chr7: 88,407,067-89,242,644 , GRCh38.p12 chr7: 88,777,753-89,613,330 TEX47, ZNF804B, 2 more genes
    nsv3919826copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840 TEX47, 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 TEX47, LOC107986817, 2014 more genes
    nsv3914094copy number variation1nstd102humanPathogenic GRCh38 chr7: 84,002,634-95,228,883 , GRCh37 chr7: 83,631,950-94,858,195 , NCBI36 chr7: 83,469,886-94,696,131 TEX47, LINC03017, 121 more genes
    nsv3915862copy number variation1nstd102humanPathogenic NCBI36 chr7: 88,152,747-89,637,882 , GRCh37 chr7: 88,314,811-89,799,946 , GRCh38 chr7: 88,685,497-90,170,632 TEX47, STEAP1, 7 more genes
    nsv3894780copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,704-159,122,532 , GRCh38.p12 chr7: 10,704-159,329,842 TEX47, RNU6-565P, 2684 more genes
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 TEX47, RPL23AP51, 2684 more genes
    nsv3909087copy number variation1nstd102humanPathogenic GRCh37 chr7: 44,935-159,126,310 , GRCh38.p12 chr7: 44,935-159,333,620 TEX47, MNX1-AS2, 2682 more genes
    nsv3908592copy number variation2nstd102humanPathogenic GRCh37 chr7: 43,361-159,119,707 , GRCh38.p12 chr7: 43,361-159,327,017 TEX47, TRGV3, 2682 more genes
    nsv6313801copy number variation1nstd102humanPathogenic GRCh37 chr7: 77,821,356-93,340,137 , GRCh38.p12 chr7: 78,192,039-93,710,825 TEX47, SOCS5P1, 140 more genes
    nsv5381780copy number variation1nstd102humanPathogenic GRCh37 chr7: 87,477,185-100,333,327 , GRCh38.p12 chr7: 87,847,870-100,735,704 TEX47, ARPC1A, 265 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 TEX47, AOC1, 2682 more genes
    nsv4352523inversion1nstd102humanPathogenic GRCh37 chr7: 20,954,043-114,556,605 , GRCh38.p12 chr7: 20,914,424-114,916,550 TEX47, ACHE, 1532 more genes
    nsv3915824copy number variation2nstd102humanUncertain significance, Conflicting interpretations of pathogenicity GRCh37 chr7: 88,192,865-89,799,946 , NCBI36 chr7: 88,030,801-89,637,882 , GRCh38 chr7: 88,563,550-90,170,632 TEX47, STEAP1, 10 more genes
    nsv3917092copy number variation1nstd102humanLikely pathogenic NCBI36 chr7: 86,846,728-91,199,124 , GRCh37 chr7: 87,008,792-91,361,188 , GRCh38 chr7: 87,379,476-91,731,873 TEX47, CDK14, 44 more genes
    nsv4729326copy number variation1nstd102humanLikely benign GRCh37 chr7: 88,248,134-89,667,010 , GRCh38.p12 chr7: 88,618,820-90,037,696 TEX47, ZNF804B, 6 more genes
    nsv3924439copy number variation1nstd102humanLikely benign NCBI36 chr7: 88,230,908-89,533,783 , GRCh37 chr7: 88,392,972-89,695,847 , GRCh38 chr7: 88,763,658-90,066,533 TEX47, ZNF804B, 4 more genes
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