itgad[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
nsv3906685	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 31,343,812-31,405,543 , GRCh38.p12 chr16: 31,332,491-31,394,222	ITGAD, ITGAM, 2 more genes
nsv3906108	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 61,451-90,294,632 , GRCh38.p12 chr16: 11,451-90,228,224	ITGAD, CKLF, 1882 more genes
nsv3904593	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 69,193-90,274,381 , GRCh38.p12 chr16: 19,193-90,207,973	ITGAD, LOC100128079, 1879 more genes
nsv3901410	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,165-90,274,695 , GRCh38.p12 chr16: 38,165-90,208,287	ITGAD, LINC02175, 1877 more genes
nsv3909417	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,165-90,163,275 , GRCh38.p12 chr16: 38,165-90,096,867	ITGAD, PRSS53, 1868 more genes
nsv3892266	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr16: 85,881-90,155,062 , GRCh38.p12 chr16: 35,881-90,088,654	ITGAD, FTLP14, 1868 more genes
nsv4685985	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 5,805,001-34,230,001 , GRCh38.p12 chr16: 5,755,000-34,995,630	ITGAD, LOC105371069, 654 more genes
nsv3913895	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 24,289,454-33,830,560 , GRCh37.p13 chr16: 24,381,953-33,923,059 , GRCh38.p12 chr16: 24,370,632-34,120,592	ITGAD, ITGAL, 310 more genes
nsv3914248	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 23,763,368-31,955,076 , GRCh38 chr16: 23,752,047-31,943,755 , NCBI36 chr16: 23,670,869-31,862,577	ITGAD, ZG16, 250 more genes
nsv3918492	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 30,703,233-35,147,508 , NCBI36 chr16: 30,610,734-35,005,009 , GRCh38 chr16: 30,691,912-36,160,463	ITGAD, KRBOX5P1, 213 more genes
nsv3924250	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 29,828,435-31,357,519 , GRCh37 chr16: 29,920,934-31,450,018 , GRCh38 chr16: 29,909,613-31,438,697	ITGAD, MIR4518, 95 more genes
nsv4436312	complex substitution	1	nstd102	human	Pathogenic	GRCh38.p12 chr16: 1,230,041-33,908,091 , GRCh37 chr16: 1,280,042-33,710,558	ITGAD, ABAT, 876 more genes
nsv3905126	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr16: 28,826,162-34,375,007 , GRCh38.p12 chr16: 28,814,841-35,140,636	ITGAD, ALDOA, 255 more genes
nsv3900464	copy number variation	1	nstd102	human	Benign	GRCh37 chr16: 30,738,551-34,194,635 , GRCh38.p12 chr16: 30,727,230-34,960,264	ITGAD, ZNF646, 139 more genes
nsv3888559	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 30,554,158-31,536,880 , GRCh38.p12 chr16: 30,542,837-31,525,559	ITGAD, SETD1A, 53 more genes
nsv3908692	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 31,198,100-31,407,832 , GRCh38.p12 chr16: 31,186,779-31,396,511	ITGAD, PYCARD-AS1, 7 more genes
nsv3895762	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 9,273,328-89,548,493 , GRCh38.p12 chr16: 9,179,471-89,482,085	ITGAD, HERC2P5, 1497 more genes
nsv1398399	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 1,279,324-31,926,800 , GRCh38.p12 chr16: 1,229,323-31,915,479	ITGAD, FLYWCH2, 817 more genes
nsv4729988	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 30,350,747-31,905,898 , GRCh38.p12 chr16: 30,339,426-31,894,577	ITGAD, VN1R3, 89 more genes
nsv1397922	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 31,154,186-31,926,800 , GRCh38.p12 chr16: 31,142,865-31,915,479	ITGAD, VN1R64P, 33 more genes

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Items: 20

Number of Variants: 20

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