cmtm7[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 17

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Number of Variants: 17

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4728631	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr3: 32,249,166-32,510,263 , GRCh38.p12 chr3: 32,207,674-32,468,771	CMTM7, CMTM8, 1 more genes
nsv6311966	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 16,710,965-41,275,270 , GRCh38.p12 chr3: 16,669,458-41,233,779	CMTM7, LOC102724104, 291 more genes
nsv3913369	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 29,206,432-35,025,542 , GRCh37.p13 chr3: 29,231,428-35,050,538 , GRCh38.p12 chr3: 29,189,937-35,009,046	CMTM7, MTND4LP9, 61 more genes
nsv3882929	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 29,689,082-34,233,218 , GRCh38.p12 chr3: 29,647,591-34,191,726	CMTM7, MIR548AY, 56 more genes
nsv3918147	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 32,322,382-36,775,606 , NCBI36 chr3: 32,338,878-36,792,101 , GRCh37 chr3: 32,363,874-36,817,097	CMTM7, TRIM71, 46 more genes
nsv3885606	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156	CMTM7, RNU4-62P, 2880 more genes
nsv3889228	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115	CMTM7, NDUFB4, 2876 more genes
nsv3880617	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391	CMTM7, RPL23AP49, 2875 more genes
nsv3905127	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 94,991-41,423,012 , NCBI36 chr3: 69,991-41,398,016 , GRCh38 chr3: 53,308-41,381,521	CMTM7, LINC02022, 540 more genes
nsv3876280	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,891-37,459,464 , GRCh38.p12 chr3: 20,213-37,417,973	CMTM7, OXTR, 460 more genes
nsv3892895	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 52,266-37,148,076 , GRCh37 chr3: 93,949-37,189,567 , NCBI36 chr3: 68,949-37,164,571	CMTM7, RPL34P11, 452 more genes
nsv3878718	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,891-36,710,181 , GRCh38.p12 chr3: 20,213-36,668,690	CMTM7, LRRC3B, 436 more genes
nsv3875913	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,891-33,958,201 , GRCh38.p12 chr3: 20,213-33,916,709	CMTM7, RPS27P11, 424 more genes
nsv3885169	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 16,923,595-45,249,923 , GRCh38.p12 chr3: 16,884,818-45,208,431	CMTM7, RNU6-243P, 382 more genes
nsv3923656	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 11,463,328-38,919,543 , NCBI36 chr3: 11,479,802-38,936,038 , GRCh37 chr3: 11,504,802-38,961,034	CMTM7, RN7SL4P, 348 more genes
nsv3888895	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr3: 25,045,365-32,691,140 , GRCh38.p12 chr3: 25,003,874-32,649,648	CMTM7, RARB, 83 more genes
nsv6313891	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 31,859,973-33,127,072 , GRCh38.p12 chr3: 31,818,481-33,085,580	CMTM7, RPL30P4, 22 more genes

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