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Items: 1 to 20 of 232

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094410copy number variation1nstd102humanUncertain significance GRCh37 chr13: 51,484,213-52,602,726 , GRCh38.p12 chr13: 50,910,077-52,028,590 ATP7B, RNA5SP29, 29 more genes
    nsv6958064copy number variation1nstd229human GRCh38 chr13: 51,831,746-51,838,233 , GRCh37.p13 chr13: 52,405,882-52,412,369 TMEM272
    nsv6955562copy number variation1nstd229human GRCh38 chr13: 51,593,867-51,848,036 , GRCh37.p13 chr13: 52,168,003-52,422,172 RN7SL413P, TMEM272, 4 more genes
    nsv6953503copy number variation1nstd229human GRCh38 chr13: 51,819,249-51,827,273 , GRCh37.p13 chr13: 52,393,385-52,401,409 TMEM272
    nsv6952435copy number variation1nstd229human GRCh38 chr13: 48,165,561-51,834,243 , GRCh37.p13 chr13: 48,739,697-52,408,379 LPAR6, RNY4P30, 77 more genes
    nsv6952289copy number variation1nstd229human GRCh38 chr13: 46,982,261-52,142,641 , GRCh37.p13 chr13: 47,556,396-52,716,777 KCNRG, RNA5SP28, 99 more genes
    nsv6951969copy number variation1nstd229human GRCh38 chr13: 45,143,357-52,624,108 , GRCh37.p13 chr13: 45,717,492-53,198,243 SNRPGP14, EBPL, 158 more genes
    nsv6944555copy number variation1nstd229human GRCh38 chr13: 51,841,101-51,845,200 , GRCh37.p13 chr13: 52,415,237-52,419,336 TMEM272
    nsv6944523copy number variation1nstd229human GRCh38 chr13: 51,834,560-51,836,363 , GRCh37.p13 chr13: 52,408,696-52,410,499 TMEM272
    nsv6944138copy number variation1nstd229human GRCh38 chr13: 49,633,124-51,990,526 , GRCh37.p13 chr13: 50,207,260-52,564,662 LOC107984561, RPL5P31, 50 more genes
    nsv6943665copy number variation1nstd229human GRCh38 chr13: 51,817,015-51,845,247 , GRCh37.p13 chr13: 52,391,151-52,419,383 TMEM272
    nsv6941985copy number variation1nstd229human GRCh38 chr13: 51,745,017-52,075,317 , GRCh37.p13 chr13: 52,319,153-52,649,453 UTP14C, DHRS12, 9 more genes
    nsv6938473copy number variation1nstd229human GRCh38 chr13: 51,742,952-52,015,459 , GRCh37.p13 chr13: 52,317,088-52,589,595 DHRS12, WDFY2, 7 more genes
    nsv6637534copy number variation1nstd102humanUncertain significance GRCh37 chr13: 52,024,106-52,496,419 , GRCh38.p12 chr13: 51,449,970-51,922,283 RNU6-65P, LOC107984561, 14 more genes
    nsv6634431copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,253,848-115,108,937 , GRCh38.p12 chr13: 18,679,708-114,343,462 MTUS2-AS1, LOC105370213, 1330 more genes
    nsv6622061copy number variation1nstd224human GRCh37 chr13: 52,367,207-52,439,890 , GRCh38.p12 chr13: 51,793,071-51,865,754 DHRS12, LOC107984561, 2 more genes
    nsv6621936copy number variation1nstd224human GRCh37 chr13: 52,100,822-52,440,184 , GRCh38.p12 chr13: 51,526,686-51,866,048 TMEM272, WDFY2, 8 more genes
    nsv6489538copy number variation1nstd223human GRCh38 chr13: 51,745,101-52,075,300 , GRCh37.p13 chr13: 52,319,237-52,649,436 UTP14C, NEK5, 9 more genes
    nsv6481876copy number variation1nstd223human GRCh38 chr13: 51,834,560-51,836,363 , GRCh37.p13 chr13: 52,408,696-52,410,499 TMEM272
    nsv6477443copy number variation1nstd223human GRCh38 chr13: 51,819,249-51,827,280 , GRCh37.p13 chr13: 52,393,385-52,401,416 TMEM272
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