nsmce2[All Fields] AND 1[has_clinical] - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4455544	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 126,179,381-126,241,524 , GRCh38.p12 chr8: 125,167,139-125,229,282	NSMCE2
nsv7097785	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 126,369,441-126,370,080 , GRCh38.p12 chr8: 125,357,199-125,357,838	NSMCE2
nsv4675167	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr8: 126,178,155-126,244,643 , GRCh38.p12 chr8: 125,165,913-125,232,401	NSMCE2
nsv3912704	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr8: 126,171,172-126,324,448 , GRCh37 chr8: 126,101,990-126,255,266 , GRCh38 chr8: 125,089,748-125,243,024	NSMCE2, WASHC5
nsv3923568	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr8: 126,165,978-126,238,485 , GRCh37 chr8: 126,096,796-126,169,303 , GRCh38 chr8: 125,084,554-125,157,061	NSMCE2, WASHC5
nsv6312901	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 126,163,393-126,379,127 , GRCh38.p12 chr8: 125,151,151-125,366,885	NSMCE2, RN7SL329P
nsv3902676	copy number variation	1	nstd102	human	Benign	GRCh37 chr8: 126,082,565-126,611,303 , GRCh38.p12 chr8: 125,070,323-125,599,059	NSMCE2, LINC02964, 3 more genes
nsv7097650	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 126,036,859-126,379,127 , GRCh38.p12 chr8: 125,024,617-125,366,885	NSMCE2, RN7SL329P, 1 more genes
nsv3903593	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 126,358,525-126,559,524 , GRCh38.p12 chr8: 125,346,283-125,547,282	NSMCE2, TRIB1, 1 more genes
nsv6637224	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 112,234,557-133,668,379 , GRCh38.p12 chr8: 111,222,328-132,656,133	NSMCE2, RNU4-37P, 220 more genes
nsv3876297	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 114,508,086-129,040,004 , GRCh38.p12 chr8: 113,495,857-128,027,758	NSMCE2, ZHX1-C8orf76, 172 more genes
nsv3914003	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 114,369,859-127,797,514 , GRCh38 chr8: 113,288,454-126,716,087 , GRCh37 chr8: 114,300,683-127,728,332	NSMCE2, RNU6-442P, 154 more genes
nsv4455511	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 124,120,772-135,265,846 , GRCh38.p12 chr8: 123,108,532-134,253,603	NSMCE2, MTSS1, 148 more genes
nsv7148124	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 118,185,471-126,635,744 , GRCh38.p12 chr8: 117,173,232-125,623,500	NSMCE2, LINC02964, 115 more genes
nsv4457220	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 123,074,293-131,113,892 , GRCh38.p12 chr8: 122,062,054-130,101,646	NSMCE2, ZHX1-C8orf76, 117 more genes
nsv3915173	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 3,938-146,274,826 , GRCh37.p13 chr8: 13,938-146,304,022 , GRCh38.p12 chr8: 63,938-145,078,636	NSMCE2, RN7SL474P, 2109 more genes
nsv3901821	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 10,213-146,293,414 , GRCh38.p12 chr8: 60,213-145,068,028	NSMCE2, TBC1D31, 2109 more genes
nsv4349554	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385	NSMCE2, LOC101929488, 2105 more genes
nsv3916777	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 158,048-146,295,771 , GRCh38 chr8: 208,048-145,070,385 , NCBI36 chr8: 148,048-146,266,575	NSMCE2, RPL5P22, 2105 more genes
nsv3898123	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr8: 158,049-146,295,771 , GRCh38.p12 chr8: 208,049-145,070,385	NSMCE2, SPAG1, 2105 more genes

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Number of Variants: 20

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Search results

Items: 1 to 20 of 63

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Number of Variants: 20

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