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Items: 1 to 20 of 531

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7141080insertion1nstd232human GRCh37.p13 chr12: 443,590-443,590 , GRCh38.p12 chr12: 334,424-334,424 KDM5A
    nsv7098813copy number variation1nstd102humanPathogenic GRCh37 chr12: 176,047-34,179,852 , GRCh38.p12 chr12: 66,881-34,026,917 TDGP1, RPS4XP14, 680 more genes
    nsv7074368inversion1nstd229human GRCh38 chr12: 340,695-349,356 , GRCh37.p13 chr12: 449,861-458,522 KDM5A
    nsv7073819inversion1nstd229human GRCh38 chr12: 209,911-509,567 , GRCh37.p13 chr12: 319,077-618,733 B4GALNT3, LOC105369594, 5 more genes
    nsv7064581inversion1nstd229human GRCh38 chr12: 98,201-316,224 , GRCh37.p13 chr12: 282,465-425,390 IQSEC3-AS1, SLC6A12, 7 more genes
    nsv7064565inversion1nstd229human GRCh38 chr12: 348,321-371,103 , GRCh37.p13 chr12: 457,487-480,269 KDM5A
    nsv7059434inversion1nstd229human GRCh38 chr12: 372,635-565,245 , GRCh37.p13 chr12: 481,801-674,411 CCDC77, B4GALNT3, 3 more genes
    nsv6917926copy number variation1nstd229human GRCh38 chr12: 323,157-645,016 , GRCh37.p13 chr12: 432,323-754,182 B4GALNT3, NINJ2, 6 more genes
    nsv6917747copy number variation1nstd229human GRCh38 chr12: 325,434-326,613 , GRCh37.p13 chr12: 434,600-435,779 KDM5A
    nsv6917607copy number variation1nstd229human GRCh38 chr12: 191,283-1,336,922 , GRCh37.p13 chr12: 300,449-1,446,088 RNU7-103P, NINJ2, 18 more genes
    nsv6917168copy number variation1nstd229human GRCh38 chr12: 163,567-522,136 , GRCh37.p13 chr12: 282,465-631,302 SLC6A12-AS1, LOC105369594, 8 more genes
    nsv6916580copy number variation1nstd229human GRCh38 chr12: 385,701-565,300 , GRCh37.p13 chr12: 494,867-674,466 B4GALNT3, CCDC77, 3 more genes
    nsv6914618copy number variation1nstd229human GRCh38 chr12: 262,012-284,446 , GRCh37.p13 chr12: 371,178-393,612 SLC6A13, KDM5A
    nsv6911426copy number variation1nstd229human GRCh38 chr12: 363,901-431,300 , GRCh37.p13 chr12: 473,067-540,466 CCDC77, KDM5A, 1 more genes
    nsv6911314copy number variation1nstd229human GRCh38 chr12: 237,370-427,821 , GRCh37.p13 chr12: 346,536-536,987 LOC105369594, LOC102723544, 3 more genes
    nsv6906257copy number variation1nstd229human GRCh38 chr12: 321,302-321,389 , GRCh37.p13 chr12: 430,468-430,555 KDM5A
    nsv6906238copy number variation1nstd229human GRCh38 chr12: 369,012-372,132 , GRCh37.p13 chr12: 478,178-481,298 KDM5A
    nsv6904973copy number variation1nstd229human GRCh38 chr12: 378,930-394,074 , GRCh37.p13 chr12: 488,096-503,240 CCDC77, KDM5A, 1 more genes
    nsv6904671copy number variation1nstd229human GRCh38 chr12: 330,518-580,767 , GRCh37.p13 chr12: 439,684-689,933 B4GALNT3, LOC105369594, 3 more genes
    nsv6903167copy number variation1nstd229human GRCh38 chr12: 287,570-432,783 , GRCh37.p13 chr12: 396,736-541,949 LOC105369594, KDM5A, 1 more genes
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