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Items: 1 to 20 of 199

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5883200copy number variation1nstd209human GRCh38 chr16: 81,042,597-81,043,916 , GRCh37.p13 chr16: 81,076,202-81,077,521 ATMIN
    nsv5529223copy number variation1nstd206human GRCh38 chr16: 81,038,191-81,038,808 , GRCh37.p13 chr16: 81,071,796-81,072,413 ATMIN, CENPN-AS1
    nsv5518867copy number variation1nstd206human GRCh38 chr16: 80,287,955-81,045,090 , GRCh37.p13 chr16: 80,321,852-81,078,695 , DYNLRB2-AS1, 8 more genes
    nsv5380217translocation1nstd200human GRCh38 chr16: 81,045,297-81,045,297 , GRCh38 chr18: 52,198,797-52,198,797 , GRCh37.p13 chr16: 81,078,902-81,078,902 , GRCh37.p13 chr18: 49,725,167-49,725,167 LOC105372121, ATMIN
    nsv5380216translocation1nstd200human GRCh38 chr16: 81,035,838-81,035,838 , GRCh38 chr17: 12,859,143-12,859,143 , GRCh37.p13 chr16: 81,069,443-81,069,443 , GRCh37.p13 chr17: 12,762,460-12,762,460 ARHGAP44, ATMIN, 1 more genes
    nsv5336752translocation1nstd200human GRCh37 chr16: 81,069,443-81,069,443 , GRCh37 chr17: 12,762,460-12,762,460 , GRCh38.p12 chr16: 81,035,838-81,035,838 , GRCh38.p12 chr17: 12,859,143-12,859,143 ARHGAP44, ATMIN, 1 more genes
    nsv5322354translocation1nstd204human GRCh37.p13 chr17: 12,762,460-12,762,460 , GRCh38.p13 chr17: 12,859,143-12,859,143 , GRCh38.p13 chr16: 81,035,838-81,035,838 , GRCh37.p13 chr16: 81,069,443-81,069,443 ARHGAP44, ATMIN, 1 more genes
    nsv5013455copy number variation1nstd200human GRCh38 chr16: 81,018,326-81,105,982 , GRCh37.p13 chr16: 81,051,931-81,139,587 PKD1L2, ATMIN, 6 more genes
    nsv5009643copy number variation1nstd200human GRCh38 chr16: 81,047,674-81,050,667 , GRCh37.p13 chr16: 81,081,279-81,084,272 ATMIN
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    nsv4729841copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 80,483,625-82,044,152 , GRCh38.p12 chr16: 80,449,728-82,010,547 GCSH, PLCG2, 25 more genes
    nsv4685754copy number variation1nstd102humannot provided GRCh37 chr16: 61,524,229-90,155,062 , GRCh38.p12 chr16: 61,490,325-90,088,654 LOC100422319, MLYCD, 547 more genes
    nsv4680010copy number variation1nstd189human GRCh37.p13 chr16: 80,886,227-81,577,179 , GRCh38.p12 chr16: 80,852,330-81,543,574 GCSH, GAN, 14 more genes
    nsv4675087copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 80,476,611-82,397,606 , GRCh38.p12 chr16: 80,442,714-82,364,001 GCSH, HSD17B2, 31 more genes
    nsv4628520copy number variation1nstd183human GRCh37 chr16: 80,886,727-81,097,625 , GRCh38.p12 chr16: 80,852,830-81,064,020 ATMIN, CENPN, 4 more genes
    nsv4626158copy number variation1nstd183human GRCh37 chr16: 81,069,171-81,070,144 , GRCh38.p12 chr16: 81,035,566-81,036,539 CENPN-AS1, ATMIN
    nsv4457298copy number variation1nstd102humanUncertain significance GRCh37 chr16: 80,892,482-81,147,086 , GRCh38.p12 chr16: 80,858,585-81,113,481 CENPN, LOC105371361, 8 more genes
    nsv4457074copy number variation1nstd102humanUncertain significance GRCh37 chr16: 79,254,648-84,827,672 , GRCh38.p12 chr16: 79,220,751-84,794,066 MEAK7, LOC654780, 74 more genes
    nsv4456228copy number variation1nstd102humanUncertain significance GRCh37 chr16: 80,892,672-81,133,120 , GRCh38.p12 chr16: 80,858,775-81,099,515 ATMIN, CENPN, 7 more genes
    nsv4436581complex substitution1nstd102humanUncertain significance GRCh38.p12 chr16: 56,334,777-90,074,947 , GRCh37 chr16: 56,368,689-90,141,355 AARS1, AP1G1, 662 more genes
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